Genomic sequencing research in pediatric cancer care: Decision-making, attitudes, and perceived utility among adolescents and young adults and their parents
(Posted May 18, 2024 4PM)
Public Attitudes, Interests, and Concerns Regarding Polygenic Embryo Screening
(Posted May 14, 2024 3PM)
Placental DNA methylation signatures of prenatal air pollution exposure and potential effects on birth outcomes: an analysis of three prospective cohorts
(Posted May 09, 2024 6PM)
Global, regional, and national burden of thalassemia, 1990–2021: a systematic analysis for the global burden of disease study 2021
(Posted May 09, 2024 6PM)
Karim Jalisa Lynn, et al. Journal of medical Internet research 2024 0 0. e53327
A national postgraduate nurse practitioner and physician assistant fellowship in cystic fibrosis: An innovative approach to the provider shortage in complex and rare disease.
Cynthia J Brady et al. J Am Assoc Nurse Pract 2024
Adolescents' implicit and explicit attitudes toward their peers with genetic conditions.
Tasha Wainstein et al. J Adolesc 2024
Australian public perspectives on genomic newborn screening: which conditions should be included?
Fiona Lynch et al. Hum Genomics 2024 18(1) 45
Clinical exome sequencing by general pediatricians: high clinical utility and no evidence of inappropriate testing.
Danya Salah Baz et al. Front Pediatr 2024 121392444
Clinical Genetic and Genomic Testing in Congenital Heart Disease and Cardiomyopathy.
Mahati Pidaparti et al. J Clin Med 2024 13(9)
Clinical Practice Patterns in Sickle Cell Disease Treatment: Disease-Modifying and Potentially Curative Therapies.
Luisanna M Sánchez et al. J Pediatr Hematol Oncol 2024
Exome sequencing in every pregnancy? Results of trio exome sequencing in structurally normal fetuses.
Michal Levy et al. Prenat Diagn 2024
New Insights beyond Established Norms: A Scoping Review of Genetic Testing for Infertile Men.
Hamid Kalantari et al. Urol J 2024
Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis and pregnancy outcomes of fetuses with polyhydramnios.
Yanyan Liu et al. J Matern Fetal Neonatal Med 2024 37(1) 2344089
Short developmental milestone risk assessment tool to identify Duchenne muscular dystrophy in primary care.
Paula van Dommelen et al. Orphanet J Rare Dis 2024 19(1) 192
Risk prediction model based on machine learning for predicting miscarriage among pregnant patients with immune abnormalities.
Yue Wu et al. Front Pharmacol 2024 151366529
Clinical and genomic landscape of RAS mutations in gynecologic cancers.
Ji Son et al. Clin Cancer Res 2024
Cost-Effectiveness of Lovotibeglogene Autotemcel (Lovo-Cel) Gene Therapy for Patients with Sickle Cell Disease and Recurrent Vaso-Occlusive Events in the United States.
William L Herring et al. Pharmacoeconomics 2024
Diagnosis, treatment, and surveillance of Diamond-Blackfan anaemia syndrome: international consensus statement.
Marcin W Wlodarski et al. Lancet Haematol 2024 11(5) e368-e382
Genetic counseling access and service delivery in New York State is variable for parents of infants with complex CFTR genotypes conferring uncertain phenotypes.
Denise M Kay et al. Pediatr Pulmonol 2024
It is Time to Screen for Homozygous Familial Hypercholesterolemia in the United States.
Samuel S Gidding et al. Glob Heart 2024 19(1) 43
Test performance and clinical utility of expanded non-invasive prenatal test: Experience on 71,883 unselected routine cases from one single center.
Monica Faieta et al. Prenat Diagn 2024
Utility of next generation sequencing in paediatric neurological disorders: experience from South Africa.
Magriet van Niekerk et al. Eur J Hum Genet 2024
Walking the tightrope: Fertility preservation among hereditary breast and ovarian Cancer syndrome Previvors.
Sharonne Holtzman et al. Gynecol Oncol 2024 186176-181
Adenosine Deaminase (ADA)-Deficient Severe Combined Immunodeficiency Unmasked by Persistent Lymphopenia and Prolonged Severe SARS-CoV-2 Infection in a Three-Week-Old Neonate.
Benslimane Zaineb, et al. Cureus 2024 0 0. (4) e57697
Advancing Newborn Screening Long-Term Follow-Up: Integration of Epic-Based Registries, Dashboards, and Efficient Workflows.
Katherine Raboin et al. Int J Neonatal Screen 2024 10(2)
An Opportunity to Fill a Gap for Newborn Screening of Neurodevelopmental Disorders.
Wendy K Chung et al. Int J Neonatal Screen 2024 10(2)
Approach and Management of Pregnancies with Risk Identified by Non-Invasive Prenatal Testing.
Miruna Gug et al. J Pers Med 2024 14(4)
Assessing the Benefits and Harms Associated with Early Diagnosis from the Perspective of Parents with Multiple Children Diagnosed with Duchenne Muscular Dystrophy.
Oindrila Bhattacharyya et al. Int J Neonatal Screen 2024 10(2)
Clinical Decision Analysis of Genetic Evaluation and Testing in 1013 Intensive Care Unit Infants with Congenital Heart Defects Supports Universal Genetic Testing.
Benjamin M Helm et al. Genes (Basel) 2024 15(4)
Cystic fibrosis newborn screening in Switzerland - evaluation and scenarios for improvement after 11 years of follow-up.
Esl Pedersen et al. J Cyst Fibros 2024
Danish Diabetes Birth Registry 2: a study protocol of a national prospective cohort study to monitor outcomes of pregnancies of women with pre-existing diabetes.
Sine Knorr et al. BMJ Open 2024 14(4) e082237
Evidence-based recommendations for delivering the diagnosis of X & Y chromosome multisomies in children, adolescents, and young adults: an integrative review.
Kirsten A Riggan et al. BMC Pediatr 2024 24(1) 263
International Perspectives of Extended Genetic Sequencing When Used as Part of Newborn Screening to Identify Cystic Fibrosis.
Corinna C A Clark et al. Int J Neonatal Screen 2024 10(2)
Long-Term Follow-Up Cares and Check Initiative: A Program to Advance Long-Term Follow-Up in Newborns Identified with a Disease through Newborn Screening.
Mei Lietsch et al. Int J Neonatal Screen 2024 10(2)
Navigating the outcome maze: a scoping review of outcomes and instruments in clinical trials in genetic neurodevelopmental disorders and intellectual disability.
Annelieke R Müller et al. Ther Adv Rare Dis 2024 526330040241245721
Newborn Screening Today and Tomorrow: A Brief Report from the International Primary Immunodeficiencies Congress.
Leire Solis et al. Int J Neonatal Screen 2024 10(2)
Prenatal Diagnosis by Trio Clinical Exome Sequencing: Single Center Experience.
Katia Margiotti et al. Curr Issues Mol Biol 2024 46(4) 3209-3217
Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing.
Anett Illés et al. BMC Med Genomics 2024 17(1) 98
Understanding the Awareness of Prenatal Genetic Screening Tests Among Pregnant Women in India: A Cross-Sectional Study.
Sangeetha Arumugam et al. Cureus 2024 16(3) e56932
Understanding the psychological impact of identifying carrier status on young adults: A qualitative study exploring peer reactions.
Edie Bowen et al. J Genet Couns 2024
Artificial Intelligence (AI) for Early Diagnosis of Retinal Diseases.
Uday Pratap Singh Parmar et al. Medicina (Kaunas) 2024 60(4)
Use of Digitalisation and Machine Learning Techniques in Therapeutic Intervention at Early Ages: Supervised and Unsupervised Analysis.
María Consuelo Sáiz-Manzanares et al. Children (Basel) 2024 11(4)
Associations between genomic aberrations, increased nuchal translucency, and pregnancy outcomes: a comprehensive analysis of 2,272 singleton pregnancies in women under 35.
Jia Huang et al. Front Med (Lausanne) 2024 111376319
Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium.
Erica Soster et al. Mol Cytogenet 2024 17(1) 9
Cost-effectiveness of BRCA1 testing at time of obstetrical prenatal carrier screening for cancer prevention.
Shayan M Dioun et al. Am J Obstet Gynecol 2024
EXPANDED NEWBORN SCREENING FOR INBORN ERRORS OF IMMUNITY: THE EXPERIENCE OF TUSCANY.
Silvia Ricci et al. J Allergy Clin Immunol Pract 2024
Navigating equity in global access to genome therapy expanding access to potentially transformative therapies and benefiting those in need requires global policy changes.
Tsung-Ling Lee et al. Front Genet 2024 151381172
Postpartum Breast Cancer and Survival in Women With Germline BRCA Pathogenic Variants.
Zhenzhen Zhang et al. JAMA Netw Open 2024 7(4) e247421
Stigma associated with genetic testing for rare diseases-causes and recommendations.
Gareth Baynam et al. Front Genet 2024 151335768
Translational Research and Health Equity: Gene Therapies for Sickle Cell Disease as a Case Study.
Mary A Majumder et al. Ethics Hum Res 2024 46(3) 34-39
Accepting or declining preconception expanded carrier screening: An exploratory study with 407 couples.
Ariane J A G Van Tongerloo et al. J Genet Couns 2024
Expanding Access to Noninvasive Prenatal Diagnosis for Monogenic Conditions to Consanguineous Families.
Britt Hanson et al. Clin Chem 2024
Exploration of clinical and ethical issues in an expanded newborn metabolic screening programme: a qualitative interview study of healthcare professionals in Hong Kong.
O M Y Ngan et al. Hong Kong Med J 2024
Impact of Race, Socioeconomic Status, and Geography on Healthcare Outcomes for Children With Sickle Cell Disease in the United States: A Scoping Review.
Sameerah Wahab et al. Cureus 2024 16(3) e56089
Prenatal screening after preimplantation genetic testing for aneuploidy: time to evaluate old strategies.
María Gabriela Palacios-Verdú et al. Reprod Biomed Online 2024 48(6) 103761
Medication Usage Record-Based Predictive Modeling of Neurodevelopmental Abnormality in Infants under One Year: A Prospective Birth Cohort Study.
Tianyi Zhou et al. Healthcare (Basel) 2024 12(7)
Clinical application value of pre-pregnancy carrier screening in Chinese Han childbearing population.
Li Tan et al. Mol Genet Genomic Med 2024 12(4) e2425
Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID.
Deanna M Green et al. Pediatrics 2024
Evaluating thromboprophylaxis in the sickle cell disease population: Navigating the evidence gap.
Jennifer Davila et al. Br J Haematol 2024
Impact of a Genetic Diagnosis for a Child's Autism on Parental Perceptions.
Julia Wynn et al. J Autism Dev Disord 2024
Newborn Screening for Severe T and B Cell Lymphopenia Using TREC/KREC Detection: A Large-Scale Pilot Study of 202,908 Newborns.
Andrey V Marakhonov et al. J Clin Immunol 2024 44(4) 93
Non-invasive prenatal test identifies circulating cell-free DNA chromosomal abnormalities derived from clonal hematopoiesis in aggressive hematological malignancies.
Valentina Giudice et al. Clin Exp Med 2024 24(1) 69
The book is just being written: The enduring journey of parents of children with emerging- ultrarare disorders.
Bethany Stafford-Smith et al. J Genet Couns 2024
A rapid PCR-free next-generation sequencing method for comprehensive diagnosis of chromosome disease syndromes in prenatal samples.
Hong Su et al. Medicine (Baltimore) 2024 103(13) e37610
Current Methods of Newborn Screening Follow-Up for Sickle Cell Disease Are Highly Variable and without Quality Assurance: Results from the ENHANCE Study.
Najibah Galadanci et al. Int J Neonatal Screen 2024 10(1)
Iowa Newborn Screening Program Experience with Hemoglobinopathy Screening over the Last Two Decades and Its Increasing Global Relevance.
Ryan Jilek et al. Int J Neonatal Screen 2024 10(1)
Psychosocial Impact of a True-Positive, False-Positive, or Inconclusive Newborn Bloodspot Screening Result: A Questionnaire Study among Parents.
Lieke M van den Heuvel et al. Int J Neonatal Screen 2024 10(1)
Towards genomic-Newborn Screening: Technical feasibility of Exome Sequencing starting from dried blood spots.
Alessia Mauri et al. Mol Genet Metab Rep 2024 39101074
Ultrasonographic Fetal Nuchal Translucency Measurements and Cytogenetic Outcomes.
Kara Bellai-Dussault et al. JAMA Netw Open 2024 7(3) e243689
Equitable Artificial Intelligence in Obstetrics, Maternal-Fetal Medicine, and Neonatology.
Ryan M McAdams et al. Obstet Gynecol 2024
Parsimonious Waveform-derived Features consisting of Pulse Arrival Time and Heart Rate Variability Predicts the Onset of Septic Shock.
Moamen M Soliman et al. Biomed Signal Process Control 2024 92
Predictive value of ultrasonic artificial intelligence in placental characteristics of early pregnancy for gestational diabetes mellitus.
Huien Zhou et al. Front Endocrinol (Lausanne) 2024 151344666
Preparing for the bedside-optimizing a postpartum depression risk prediction model for clinical implementation in a health system.
Yifan Liu et al. J Am Med Inform Assoc 2024
The Effectiveness of Artificial Intelligence in Assisting Mothers with Assessing Infant Stool Consistency in a Breastfeeding Cohort Study in China.
Jieshu Wu et al. Nutrients 2024 16(6)
The Importance of Vaccination, Variants and Time Point of SARS-CoV-2 Infection in Pregnancy for Stillbirth and Preterm Birth Risk: An Analysis of the CRONOS Register Study.
Iannaccone Antonella, et al. Journal of clinical medicine 2024 0 0. (6)
A scoping review exploring cure definitions and language for inherited hemoglobinopathies.
Marilyn S Baffoe-Bonnie et al. Genet Med Open 2024 2
An AI-based approach driven by genotypes and phenotypes to uplift the diagnostic yield of genetic diseases.
S Zucca et al. Hum Genet 2024
Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children.
Danya F Vears et al. Twin Res Hum Genet 2024 1-8
Molecular autopsy for fetal structural anomaly: diagnostic and clinical utility of multidisciplinary team approach.
E Wall et al. Ultrasound Obstet Gynecol 2024
Newborn Screening: Current Practice and Our Journey over the Last 60 Years.
Jing Cao et al. J Appl Lab Med 2024
Parent perspectives following newborn screening resulting in diagnoses of fragile X syndrome or fragile X premutation.
Allyson Corbo et al. Res Dev Disabil 2024 148104719
Ready for polygenic risk scores? An analysis of regulation of preimplantation genetic testing in European countries.
M Siermann et al. Hum Reprod 2024
Machine learning-enabled maternal risk assessment for women with pre-eclampsia (the PIERS-ML model): a modelling study.
Tünde Montgomery-Csobán et al. Lancet Digit Health 2024 6(4) e238-e250
Mendelian randomization supports genetic liability to hospitalization for COVID-19 as a risk factor of pre-eclampsia.
Wu Weizhen, et al. Frontiers in cardiovascular medicine 2024 0 0. 1327497
An International Learning Collaborative Phase 2 Trial for Haploidentical Bone Marrow Transplant in Sickle Cell Disease.
Adetola A Kassim et al. Blood 2024
Current state of gene therapy in sickle cell disease.
Mei San Tang et al. Vox Sang 2024
Development of a Low Cost Semiquantitative Polymerase Chain Reaction Assay for Molecular Diagnosis of Williams Syndrome.
Dinali M Ranaweera et al. Clin Lab 2024 70(3)
Experiences and concerns of parents of children with a 16p11.2 deletion or duplication diagnosis: a reflexive thematic analysis.
Charlotte E Butter et al. BMC Psychol 2024 12(1) 137
Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth disease.
Christopher J Record et al. Brain 2024
Artificial intelligence in imaging in the first trimester of pregnancy: a systematic review.
Emma Umans et al. Fetal Diagn Ther 2024
Identifying non-adult attention-deficit/hyperactivity disorder individuals using a stacked machine learning algorithm using administrative data population registers in a universal healthcare system.
David Roche et al. JCPP Adv 2024 4(1) e12193
Predicting risk of preterm birth in singleton pregnancies using machine learning algorithms.
Qiu-Yan Yu et al. Front Big Data 2024 71291196
'Something that helped the whole picture': Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service.
Hannah McInnes-Dean et al. Prenat Diagn 2024
An extra X chromosome among adult women in the Million Veteran Program: A more benign perspective of trisomy X.
Shanlee M Davis et al. Am J Med Genet C Semin Med Genet 2024 e32083
Clinical value of screening prenatal ultrasound combined with chromosomal microarrays in prenatal diagnosis of chromosomal abnormalities.
Hongru Jiang et al. J Matern Fetal Neonatal Med 2024 37(1) 2324348
De novo copy number variations in candidate genomic regions in patients of severe autism spectrum disorder in Vietnam.
Hoa Thi Phuong Bui et al. PLoS One 2024 19(3) e0290936
Dental caries in the permanent dentition and health-related quality of life among children and adolescents with sickle cell disease.
Vera Lúcia Duarte da Costa Mendes et al. Cien Saude Colet 2024 29(3) e06752023
Diagnostic utility of exome sequencing followed by research reanalysis in human brain malformations.
Daniz Kooshavar et al. Brain Commun 2024 6(2) fcae056
Estimation of carrier frequencies utilizing the gnomAD database for ACMG recommended carrier screening and Finnish disease heritage conditions in non-Finnish European, Finnish, and Ashkenazi Jewish populations.
Miska Kandolin et al. Am J Med Genet A 2024 e63588
Evaluation of Nanopore Sequencing on Polar Bodies for Routine Pre-Implantation Genetic Testing for Aneuploidy.
Anna Oberle et al. Clin Chem 2024
Improving newborn screening test performance for metachromatic leukodystrophy: Recommendation from a pre-pilot study that identified a late-infantile case for treatment.
Teresa H Y Wu et al. Mol Genet Metab 2024 142(1) 108349
Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey.
Alexis Ceecee Britten-Jones et al. Sci Rep 2024 14(1) 5403
Performance of cell-free DNA testing for common fetal trisomies in triplet pregnancies.
Hoda Zakaria et al. Prenat Diagn 2024
What do parents of nonverbal and minimally verbal autistic children think about genomic autism research?
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Young Women's Perspectives on Being Screened for Hereditary Breast and Ovarian Cancer Risk During Routine Primary Care.
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Artificial Intelligence in Pediatrics: Learning to Walk Together.
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Enhancing ASD detection accuracy: a combined approach of machine learning and deep learning models with natural language processing.
Sergio Rubio-Martín et al. Health Inf Sci Syst 2024 12(1) 20
Enhancing gestational diabetes mellitus risk assessment and treatment through GDMPredictor: a machine learning approach.
J Xing et al. J Endocrinol Invest 2024
Assessment of Barriers to Referral and Appointment Wait Times for the Evaluation of Spinal Muscular Atrophy (SMA): Findings from a Web-Based Physician Survey.
Mary A Curry et al. Neurol Ther 2024
Detecting missed diagnoses of spinal muscular atrophy in genome, exome, and panel sequencing datasets.
Ben Weisburd et al. medRxiv 2024
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement.
Alessandro Geroldi et al. Pediatr Neurol 2024 1544-8
Genetic Information to Share with Parents when Newborn Screening Reveals the Presence of Sickle Cell Trait.
Narcisse Elenga et al. Int J Pediatr 2024 20248910397
The majority of parents of children undergoing genetic testing report preference for earlier genetic counseling appointments.
Cami Cochrane et al. J Genet Couns 2024
The Multiple Odysseys in Research and Clinical Care for Neurogenetic Conditions.
Anne C Wheeler et al. Am J Intellect Dev Disabil 2024 129(2) 110-115
What importance do donors and recipients attribute to the nuclear DNA-related genetic heritage of oocyte donation?
A Mayeur et al. Hum Reprod 2024
Machine Learning-Based Approach for Identifying Research Gaps: COVID-19 as a Case Study.
Abd-Alrazaq Alaa, et al. JMIR formative research 2024 0 0. e49411
Promises, Pitfalls, and Clinical Applications of Artificial Intelligence in Pediatrics.
Hansa Bhargava et al. J Med Internet Res 2024 26e49022
EVALUATION OF THE EasyNAT SARS-CoV-2 ASSAY PCR TEST FOR THE DIAGNOSIS OF SARS-CoV-2 INFECTION.
Fernández-Sánchez Fernando, et al. Journal of virological methods 2024 0 0. 114908
A holistic approach to fragile X syndrome integrated guidance for person-centred care.
Kirsten Johnson et al. J Appl Res Intellect Disabil 2024 37(3) e13214
Clinical utility of polygenic risk scores for embryo selection: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).
Theresa A Grebe et al. Genet Med 2024 101052
Describing patterns of familial cancer risk in subfertile men using population pedigree data.
Joemy M Ramsay et al. Hum Reprod 2024
Leading Risk Factors for Congenital Deafness in the Context of Universal Neonatal Screening: Our Observations in a Four-Year Retrospective Study.
Antoine Paul et al. Int J Neonatal Screen 2024 10(1)
Newborn Screening for Krabbe Disease: Status Quo and Recommendations for Improvements.
Dietrich Matern et al. Int J Neonatal Screen 2024 10(1)
Perceptions and preferences for genetic testing for sickle cell disease or trait: a qualitative study in Cameroon, Ghana and Tanzania.
Nchangwi Syntia Munung et al. Eur J Hum Genet 2024
Transition from pediatric to adult care in patients with Turner syndrome in Italy: a consensus statement by the TRAMITI project.
T Aversa et al. J Endocrinol Invest 2024
Artificial Intelligence in Obstetric Anomaly Scan: Heart and Brain.
Iuliana-Alina Enache et al. Life (Basel) 2024 14(2)
Automated identification of abnormal infant movements from smart phone videos.
E Passmore et al. PLOS Digit Health 2024 3(2) e0000432
Current Updates on Involvement of Artificial Intelligence and Machine Learning in Semen Analysis.
Manesh Kumar Panner Selvam et al. Medicina (Kaunas) 2024 60(2)
Early childhood caries detection using smartphone artificial intelligence.
E Veseli et al. Eur Arch Paediatr Dent 2024
Prediction of pregnancy-related complications in women undergoing assisted reproduction, using machine learning methods.
Chen Wang et al. Fertil Steril 2024
Revolutionizing Women's Health: A Comprehensive Review of Artificial Intelligence Advancements in Gynecology.
Marta Brandão et al. J Clin Med 2024 13(4)
APOE ε4 and Intracerebral Hemorrhage in Patients With Brain Arteriovenous Malformation.
Daniela Renedo et al. JAMA Netw Open 2024 7(2) e2355368
Diagnostic Accuracy of Creatine Kinase Isoenzyme-MM Test in Newborn Screening for Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis.
Liang Tang et al. Pediatr Neurol 2024 15384-91
Eliciting parental preferences and values for the return of additional findings from genomic sequencing.
Ilias Goranitis et al. NPJ Genom Med 2024 9(1) 10
Lived experiences of genetic diagnosis for rare disease patients: a qualitative interview study.
Antonia Modelhart et al. Orphanet J Rare Dis 2024 19(1) 68
Parental Perspectives on Early Life Screening and Genetic Testing for ASD: A Systematic Review.
Katerina Dounavi et al. J Autism Dev Disord 2024
Patient Perceptions on the Advancement of Noninvasive Prenatal Testing for Sickle Cell Disease among Black Women in the United States.
Shameka P Thomas et al. AJOB Empir Bioeth 2024 1-10
Evaluation of Informative Content on Cerebral Palsy in the Era of Artificial Intelligence: The Value of ChatGPT.
Ayse Merve Ata et al. Phys Occup Ther Pediatr 2024 1-10
Predicting preterm birth using auto-ML frameworks: a large observational study using electronic inpatient discharge data.
Deming Kong et al. Front Pediatr 2024 121330420
An update review of new therapies in sickle cell disease: the prospects for drug combinations.
Sanne Lugthart et al. Expert Opin Pharmacother 2024
Implementation of rapid genomic sequencing in safety-net neonatal intensive care units: protocol for the VIrtual GenOme CenteR (VIGOR) proof-of-concept study.
Alissa M D'Gama et al. BMJ Open 2024 14(2) e080529
Wales Infants' and childreN's Genome Service (WINGS): providing rapid genetic diagnoses for unwell children.
Emily Sloper et al. Arch Dis Child 2024
Prediction of emergency department revisits among child and youth mental health outpatients using deep learning techniques.
Simran Saggu et al. BMC Med Inform Decis Mak 2024 24(1) 42
Global Transcriptomic Analysis of Placentas from Women with Gestational SARS-CoV-2 Infection during the Third Trimester of Pregnancy.
Yiqun Tang et al. Int J Mol Sci 2024 2 (3)
Blood Spotlight Review on Gene Therapy for Sickle Cell Disease.
Edward J Benz et al. Blood 2024
Clinical evaluation of noninvasive prenatal testing for sex chromosome aneuploidies in 9,176 Korean pregnant women: a single-center retrospective study.
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Comprehensive Care in Sickle Cell Disease.
Ananya Chandra et al. Pediatr Ann 2024 53(2) e43-e46
Genetic testing of children with familial tall stature: is it worth doing?
Katerina Gregorova et al. J Clin Endocrinol Metab 2024
Knowledge gaps and confidence in counseling about aneuploidy screening and testing: A survey of prenatal care clinicians.
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Polygenic risk scores mediating functioning outcomes through cognitive and clinical features in youth at family risk and controls.
Alex G Segura et al. Eur Neuropsychopharmacol 2024 8128-37
Provider-reported experiences, barriers, and perspectives on genetic testing as part of autism diagnosis.
Amy Wang et al. PLoS One 2024 19(2) e0296942
The detection efficacy of noninvasive prenatal genetic testing (NIPT) for sex chromosome abnormalities and copy number variation and its differentiation in pregnant women of different ages.
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The effectiveness of expanded carrier screening based on next-generation sequencing for severe monogenic genetic diseases.
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The value of genomic testing in severe childhood speech disorders.
Yan Meng et al. Eur J Hum Genet 2024
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder.
Ashraf Yahia et al. Hum Genet 2024
Young adults with a 22q11.2 microdeletion and the cost of aging with complexity in a population-based context.
Sarah L Malecki et al. Genet Med 2024 101088
Deep Survival Analysis for Interpretable Time-Varying Prediction of Preeclampsia Risk.
Braden W Eberhard et al. medRxiv 2024
The Clinical Use of Artificial Intelligence and Machine Learning in Pediatrics.
Joseph R Hageman et al. Pediatr Ann 2024 53(2) e37-e38
Impact of COVID-19 pandemic in the Brazilian maternal mortality ratio: A comparative analysis of Neural Networks Autoregression, Holt-Winters exponential smoothing, and Autoregressive Integrated Moving Average models.
Cañedo Mayara Carolina, et al. PloS one 2024 0 0. (1) e0296064
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation.
Fiona Lynch et al. Int J Neonatal Screen 2024 10(1)
Clinical value of positive CNVs results by NIPT without fetal ultrasonography-identified structural anomalies.
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Clinically significant findings in a decade-long retrospective study of prenatal chromosomal microarray testing.
Joie O Olayiwola et al. Mol Genet Genomic Med 2024 e2349
Exploring Genetic Testing for Rare Disorders of Obesity: Experience and Perspectives of Pediatric Weight Management Providers.
Karyn J Roberts et al. Child Obes 2024
Gene Therapy Versus Common Care for Eligible Individuals With Sickle Cell Disease in the United States : A Cost-Effectiveness Analysis.
Anirban Basu et al. Ann Intern Med 2024
Genetic risk for attention-deficit/hyperactivity disorder predicts cognitive decline and development of Alzheimer's disease pathophysiology in cognitively unimpaired older adults.
Douglas T Leffa et al. Mol Psychiatry 2022 28(3) 1248-1255
Genomic Medicine Guidance: A Point-of-Care App for Heritable Thoracic Aortic Diseases.
Rohan Patil et al. medRxiv 2024
Incidental Detection of Classical Galactosemia through Newborn Screening for Phenylketonuria: A 10-Year Retrospective Audit to Determine the Efficacy of This Approach.
Nathan W P Cantley et al. Int J Neonatal Screen 2024 10(1)
International Atherosclerosis Society Roadmap for Familial Hypercholesterolaemia.
Gerald F Watts et al. Glob Heart 2024 19(1) 12
Landscape Analysis of Neurodevelopmental Comorbidities in Newborn Screening Conditions: Challenges and Opportunities.
Zohreh Talebizadeh et al. Int J Neonatal Screen 2024 10(1)
Preimplantation genetic testing in couples with balanced chromosome rearrangement: a four-year period real world retrospective cohort study.
Fan Zhou et al. BMC Pregnancy Childbirth 2024 24(1) 86
Real-World Outcomes in Patients with Spinal Muscular Atrophy Treated with Onasemnogene Abeparvovec Monotherapy: Findings from the RESTORE Registry.
Laurent Servais et al. J Neuromuscul Dis 2024
The Impact of Integration of a Genetic Clinic Into a Pediatric Cardiac Unit.
Ayman Elfky et al. Cureus 2024 15(12) e50941
The psychological impact of genetic testing in childhood cancer: A systematic review.
Sophie Van Hoyweghen et al. Psychooncology 2024 33(1) e6279
The Psychological Impact on Parents of Children who Receive an Inconclusive Diagnosis for Cystic Fibrosis following Newborn Screening: A Systematic Mini-Review.
Ioanna Loukou et al. Children (Basel) 2024 11(1)
Whole-genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting.
E Westenius et al. Ultrasound Obstet Gynecol 2024
Cloud-Integrated Smart Nanomembrane Wearables for Remote Wireless Continuous Health Monitoring of Postpartum Women.
Jared Matthews et al. Adv Sci (Weinh) 2024 e2307609
External evaluation of the Dynamic Criticality Index: A machine learning model to predict future need for ICU care in hospitalized pediatric patients.
Anita K Patel et al. PLoS One 2024 19(1) e0288233
Recommendations for initial diabetic retinopathy screening of diabetic patients using large language model-based artificial intelligence in real-life case scenarios.
Nikhil Gopalakrishnan et al. Int J Retina Vitreous 2024 10(1) 11
Role of artificial intelligence in early detection of congenital heart diseases in neonates.
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Radniecki, Tyler et al. Research Square July 08 2021
Editorial: Maternal SARS-CoV-2 Infection and Pregnancy Outcomes from Current Global Study Data.
Parums Dinah V, et al. Medical science monitor : international medical journal of experimental and clinical research 2021 0 0. e933831
Protein S: function, regulation, and clinical perspectives.
Majumder Rinku, et al. Current opinion in hematology 2021 0 0.
SARS-CoV-2 infection in patients with β-thalassemia: the French experience.
Jean-Mignard Estelle, et al. Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine 2021 0 0.
The COVID-19 pandemic and reproductive genetic counseling: Changes in access and service delivery at an academic medical center in the United States.
Mann Caitlin, et al. Journal of genetic counseling 2021 0 0.
COVID 19 pandemic and lockdown: A double whammy for patients with thalassemia.
Kakkar Shruti, et al. Acta bio-medica : Atenei Parmensis 2021 0 0. (3) e2021212
In Silico Identification of miRNA-lncRNA Interactions in Male Reproductive Disorder Associated with COVID-19 Infection.
Sabetian Soudabeh, et al. Cells 2021 0 0. (6)
Respiratory Telerehabilitation of Boys and Young Men with Duchenne Muscular Dystrophy in the COVID-19 Pandemic.
Sobierajska-Rek Agnieszka, et al. International journal of environmental research and public health 2021 0 0. (12)
Comorbidities are risk factors for hospitalization and serious COVID-19 illness in children and adults with sickle cell disease.
Mucalo Lana, et al. Blood advances 2021 0 0. (13) 2717-2724
SARS-CoV-2 lineage B.1.1.7 is associated with greater disease severity among hospitalised women but not men
O Stirrup et al, MEDRXIV, June 28, 2021
Expression of SARS-CoV-2 entry genes ACE2 and TMPRSS2 at single cell resolution in the peripartum decidua.
Li Qi, et al. American journal of translational research 2021 0 0. (5) 4389-4400
Inefficient Placental Virus Replication and Absence of Neonatal Cell-Specific Immunity Upon Sars-CoV-2 Infection During Pregnancy.
Tallarek Ann-Christin, et al. Frontiers in immunology 2021 0 0. 698578
Association of Sickle Cell Trait with Risk and Mortality of COVID-19: Results from the United Kingdom Biobank.
Resurreccion W Kyle, et al. The American journal of tropical medicine and hygiene 2021 0 0.
Evaluating the efficacy and safety of human anti-SARS-CoV-2 convalescent plasma in severely ill adults with COVID-19: A structured summary of a study protocol for a randomized controlled trial.
Eckhardt Christina M, et al. Trials 2020 0 0. (1) 499
Individuals with Down syndrome hospitalized with COVID-19 have more severe disease.
Malle Louise, et al. Genetics in medicine : official journal of the American College of Medical Genetics 2020 0 0. (3) 576-580
Preliminary Findings of mRNA Covid-19 Vaccine Safety in Pregnant Persons.
Shimabukuro Tom T et al. The New England journal of medicine 2021 4 (24) 2273-2282
Using BCG vaccine to enhance non-specific protection of health care workers during the COVID-19 pandemic: A structured summary of a study protocol for a randomised controlled trial in Denmark.
Madsen Anne Marie Rosendahl, et al. Trials 2020 0 0. (1) 799
[Consensus of the Genetics Branch of the Chilean Society of Pediatrics on the prioritization of people with Down syndrome and rare diseases for vaccination against SARS-CoV-2].
Faundes Victor, et al. Andes pediatrica : revista Chilena de pediatria 2021 0 0. (2) 309-315
A Patient-Focused Survey to Assess the Effects of the COVID-19 Pandemic and Social Guidelines on People with Muscular Dystrophy.
Eichinger Katy, et al. Muscle & nerve 2021 0 0.
Changes in motor function in Duchenne muscular dystrophy patients after travel restrictions due to COVID-19.
Nishizawa Hitomi, et al. Muscle & nerve 2021 0 0.
Risk Factors Associated With COVID-19 Outcomes Among People With Intellectual and Developmental Disabilities Receiving Residential Services.
Landes Scott D, et al. JAMA network open 2021 0 0. (6) e2112862
The statistical risk of diagnosing coincidental acquired hemophilia A following anti-SARS-CoV-2 vaccination.
Cittone Micol G, et al. Journal of thrombosis and haemostasis : JTH 2021 0 0.
Beneficial Effects of Remote Medical Care for Patients with Hereditary Hemorrhagic Telangiectasia during the COVID-19 Pandemic.
Gaetani Eleonora, et al. Journal of clinical medicine 2021 0 0. (11)
Impact of the COVID-19 Italian Lockdown on the Physiological and Psychological Well-Being of Children with Fragile X Syndrome and Their Families.
Di Giorgio Elisa, et al. International journal of environmental research and public health 2021 0 0. (11)
SARS-CoV-2-Morphology, Transmission and Diagnosis during Pandemic, Review with Element of Meta-Analysis.
Grudlewska-Buda Katarzyna, et al. Journal of clinical medicine 2021 0 0. (9)
COVID-19 in advanced Duchenne/Becker muscular dystrophy patients.
Levine Hagit, et al. Neuromuscular disorders : NMD 2021 0 0.
SARS-CoV-2 Infects Syncytiotrophoblast and Activates Inflammatory Responses in the Placenta.
Argueta Lissenya B, et al. bioRxiv : the preprint server for biology 2021 0 0.
Applying Genomic Epidemiology to Characterize a COVID-19 Outbreak in a Developmentally Disabled Adult Group Home Setting, Arizona.
Yaglom Hayley D et al. Frontiers in public health 2021 6 668214
How the clinical research community responded to the COVID-19 pandemic: an analysis of the COVID-19 clinical studies in ClinicalTrials.gov.
He Zhe, et al. JAMIA open 2021 0 0. (2) ooab032
Probing nano-QSAR to assess the interactions between carbon nanoparticles and a SARS-CoV-2 RNA fragment.
Zhang Fan, et al. Ecotoxicology and environmental safety 2021 0 0. 112357
Coagulation Abnormalities Due to COVID-19 in a Child with Thalassemia: Correspondence.
Mungmunpuntipantip Rujittika, et al. Indian journal of pediatrics 2021 0 0.
Sound prescriptions to mitigate the effects of COVID-19 in the population with Down syndrome.
Verd Sergio, et al. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021 0 0.
Effective high-throughput isolation of fully human antibodies targeting infectious pathogens.
Gieselmann Lutz, et al. Nature protocols 2021 0 0.
Population stratification enables modeling effects of reopening policies on mortality and hospitalization rates.
Huang Tongtong, et al. Journal of biomedical informatics 2021 0 0. 103818
Incidence Rate of COVID-19 Infection in Hemoglobinopathies: A Systematic Review and Meta-analysis.
Haghpanah Sezaneh, et al. Hemoglobin 2021 0 0. 1-9
Parsonage-turner syndrome associated with SARS-CoV2 (COVID-19) infection.
Mitry Maria A, et al. Clinical imaging 2020 0 0. 8-10
Toddler With New Onset Diabetes and Atypical Hemolytic-Uremic Syndrome in the Setting of COVID-19.
Alizadeh Faraz, et al. Pediatrics 2020 0 0. (2)
Performance of the TaqMan™ COVID-19 Pooling Kit for detection of SARS-CoV-2 in Asymptomatic and Symptomatic populations at an Institution of Higher Education
Ganz, Troy et al. medRxiv May 21 2021
COVID-19 Lung Lesion Segmentation Using a Sparsely Supervised Mask R-CNN on Chest X-rays Automatically Computed from Volumetric CTs
Ramesh, Vignav et al. arXiv May 19 2021
Implementation Research for the Evaluation of the Child Health Education and Surveillance Tool Application
Westgard, Christopher M et al. Research Square May 11 2021
Higher case fatality rate among obstetric patients with COVID-19 in the second year of pandemic in Brazil: do new genetic variants play a role?
M Libertad et al, MEDRXIV, May 8, 2021
Teletherapy for children with developmental disorders during the COVID-19 pandemic in the Philippines: a mixed-methods evaluation from the perspectives of parents and therapists
KF Eguia et al, MEDRXIV, May 9, 2021
A Cross-National Survey of People Living with Hemophilia: Impact on Daily Living and Patient Education in Central Europe.
Banchev Atanas, et al. Patient preference and adherence 2021 0 0. 871-883
Effects of the COVID-19 pandemic and lockdown on the mental and physical health of adults with Prader-Willi syndrome.
Mosbah Helena, et al. Orphanet journal of rare diseases 2021 0 0. (1) 202
Accelerating Epidemiological Investigation Analysis by Using NLP and Knowledge Reasoning: A Case Study on COVID-19.
Wang Jian, et al. AMIA ... Annual Symposium proceedings. AMIA Symposium 2021 0 0. 1258-1267
SARS-CoV-2 Infection in Hereditary Hemorrhagic Telangiectasia Patients Suggests Less Clinical Impact Than in the General Population.
Marcos Sol, et al. Journal of clinical medicine 2021 0 0. (9)
SARS-CoV-2 infection in patients with β-thalassemia: Experience from Lebanon.
Bou-Fakhredin Rayan, et al. American journal of hematology 2021 0 0.
Generation of a Sleeping Beauty transposon-based cellular system for rapid and sensitive identification of SARS-CoV-2 host dependency and restriction factors
Widera, Marek et al. bioRxiv April 27 2021
Increased VWF and Decreased ADAMTS-13 in COVID-19: Creating a Milieu for (Micro)Thrombosis.
Favaloro Emmanuel J, et al. Seminars in thrombosis and hemostasis 2021 0 0.
COV-ID: A LAMP sequencing approach for high-throughput co-detection of SARS-CoV-2 and influenza virus in human saliva
RW Thomson et al, MEDRXIV, April 23, 2021
Double stranded RNA drives anti-viral innate immune responses, sickness behavior and cognitive dysfunction dependent on dsRNA length, IFNAR1 expression and age.
McGarry Niamh, et al. Brain, behavior, and immunity 2021 0 0. 413-428
Telemedicine for adult congenital heart disease patients during the first wave of COVID-19 era: a single center experience.
Grandinetti Maria, et al. Journal of cardiovascular medicine (Hagerstown, Md.) 2021 0 0.
Life-threatening DRESS syndrome with kidney damage following severe COVID-19 in a patient with Down syndrome.
Mata Lorena, et al. BMJ case reports 2021 0 0. (4)
Trace Analysis of Emerging Virus: an Ultrasensitive ECL-Scan Imaging System for Viral Infectious Disease
Wu, Yunxia et al. Research Square April 01 2021
A rapid, cost efficient and simple method to identify current SARS-CoV-2 variants of concern by Sanger sequencing part of the spike protein gene
Jorgensen, Tue Sparholt et al. medRxiv March 29 2021
Autism Spectrum Disorder, Family Health History, and Genetics
CDC, March 2021
Viral Haplotypes in COVID-19 Patients Associated with Prolonged Viral Shedding
Wu, Yingping et al. SSRN March 25 2021
COVID-19: ORF8 Synthesizes Nitric Oxide to Break the Blood-Brain/Testi Barrier and Damage the Reproductive System
Wenzhong, Liu et al. ChemRxiv March 24 2021
v-safe COVID-19 Vaccine Pregnancy Registry
CDC, March 2021
Development of multi-epitope peptide-based vaccines against SARS-CoV-2.
Lim Hui Xuan, et al. Biomedical journal 2021 0 0. (1) 18-30
Coagulopathy of hospitalised COVID-19: A Pragmatic Randomised Controlled Trial of Therapeutic Anticoagulation versus Standard Care as a Rapid Response to the COVID-19 Pandemic (RAPID COVID COAG - RAPID Trial): A structured summary of a study protocol for a randomised controlled trial.
Sholzberg Michelle, et al. Trials 2021 0 0. (1) 202
3D U-Net For Segmentation of Covid-19-Associated Pulmonary Infiltrates Using Transfer Learning: State-Of-The-Art Results on Affordable Hardware
Bressem, Keno K et al. Research Square March 11 2021
3D U-Net for segmentation of COVID-19 associated pulmonary infiltrates using transfer learning: State-of-the-art results on affordable hardware
Bressem, Keno K. et al. arXiv January 25 2021
Having Down syndrome increases your risk of severe illness from COVID-19.
CDC, January 7, 2021
[Epidemiological and clinical profile of children with Coronavirus disease (COVID-19) at the Center for the Treatment of Epidemics and Infection Prevention (CTEIP) of the University Hospital of Donka in Conakry].
Camara Emmanuel, et al. The Pan African medical journal 2021 0 0. 363
Early use of corticosteroids in non-critical patients with COVID-19 pneumonia (PREDCOVID): a structured summary of a study protocol for a randomised controlled trial.
Salinas Mauricio, et al. Trials 2021 0 0. (1) 92
Remote assessment in adults with Autism or ADHD: A service user satisfaction survey.
Adamou Marios, et al. PloS one 2021 0 0. (3) e0249237
The Yin and Yang of traditional Chinese and Western medicine.
Fu Rao, et al. Medicinal research reviews 2021 0 0.
Direct measurement of B lymphocyte gene expression biomarkers in peripheral blood enables early prediction of seroconversion after vaccination
Huang, Dan et al. bioRxiv December 30 2020
Recent Advances in Computer Audition for Diagnosing COVID-19: An Overview
Qian, Kun et al. arXiv December 08 2020
Network of “drug-target-SARS-CoV-2 Related Genes” Through Integrated Analysis of Pharmacology and Geo Database
Hou, Jin Ping et al. Research Square December 04 2020
Glasgow Early Treatment Arm Favirpiravir (GETAFIX) for adults with early stage COVID-19: A structured summary of a study protocol for a randomised controlled trial.
Hanna Catherine R, et al. Trials 2020 0 0. (1) 935
Clinical, regional, and genetic characteristics of Covid-19 patients from UK Biobank.
Kolin David A, et al. PloS one 2020 0 0. (11) e0241264
Bioinformatic analysis of SMN1-ACE/ACE2 interactions hinted at a potential protective effect of spinal muscular atrophy against COVID-19-induced lung injury.
Li Zheng, et al. Briefings in bioinformatics 2020 0 0. (2) 1291-1296
Clinical and molecular characterization of COVID-19 hospitalized patients
Benetti, Elisa et al. medRxiv November 02 2020
A Machine Learning Study of 534,023 Medicare Beneficiaries with COVID-19: Implications for Personalized Risk Prediction
Dun, Chen et al. medRxiv October 30 2020
Single-cell expression profiles of ACE2 and TMPRSS2 reveals potential vertical transmission and fetus infection of SARS-CoV-2.
Lü Mengdie, et al. Aging 2020 0 0. (20) 19880-19897
Immunity and coagulation and fibrinolytic processes may reduce the risk of severe illness in pregnant women with coronavirus disease 2019.
Zhong Yajuan, et al. American journal of obstetrics and gynecology 2020 0 0. (4) 393.e1-393.e25
The clinical effect of Nano micelles containing curcumin as a therapeutic supplement in patients with COVID-19 and the immune responses balance changes following treatment: A structured summary of a study protocol for a randomised controlled trial.
Hassaniazad Mehdi, et al. Trials 2020 0 0. (1) 876
Clinical Spectrum of Sickle Cell Disease and COVID-19: Laboratory and Clinical Factors Associated with Morbidity and Mortality
Minniti, Caterina P et al. SSRN October 15 2020
A k-mer based approach for virus classification identifies coronavirus infections and viral associations in human and plant microbiomes
Garcia, Benjamin et al. Research Square October 13 2020
A rapid and cost-effective multiplex ARMS-PCR method for the simultaneous genotyping of the circulating SARS-CoV-2 phylogenetic clades
Islam, Md Tanvir et al. medRxiv October 13 2020
Hybrid-COVID: A novel hybrid 2D/3D CNN based on cross-domain adaptation approach for COVID-19 screening from chest X-ray images
Bayoudh, Khaled et al. Research Square October 09 2020
Placental maternal vascular malperfusion affecting late fetuses development and multi-organ infection caused by SARS-CoV-2
Behling, J A K et al. Research Square October 09 2020
The metabolic and immunological characteristics of pregnant women with COVID-19 and their neonates.
Zhou Jingjiao, et al. European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology 2020 0 0. (3) 565-574
Renin Angiotensin System, COVID-19 and Male Fertility: Any Risk for Conceiving?
Pascolo Lorella, et al. Microorganisms 2020 0 0. (10)
SARS-CoV-2 cell entry gene ACE2 expression in immune cells that infiltrate the placenta in infection-associated preterm birth
Lye, Phetcharawan et al. medRxiv September 29 2020
Evaluation of the potency of FDA-approved drugs on wild type and mutant SARS-CoV-2 helicase (Nsp13).
Ugurel Osman Mutluhan, et al. International journal of biological macromolecules 2020 0 0. 1687-1696
Personalized predictive models for symptomatic COVID-19 patients using basic preconditions: Hospitalizations, mortality, and the need for an ICU or ventilator.
Wollenstein-Betech Salomón, et al. International journal of medical informatics 2020 0 0. 104258
Data on COVID-19 during Pregnancy
CDC, August 2020
The effect of prostacyclin (Iloprost) infusion at a dose of 1 ng/kg/min for 72 hours compared to placebo in mechanically ventilated patients with COVID-19: A structured summary of a study protocol for a randomized controlled trial.
Johansson Pär Ingemar, et al. Trials 2020 0 0. (1) 746
The novel roles of choline transporter-like 1 and 2 in ethanolamine transport
Taylor, Adrian et al. bioRxiv August 28 2020
Changes in Cause-of-Death Attribution During the Covid-19 Pandemic: Association with Hospital Quality Metrics and Implications for Future Research
Fairman, Kathleen A et al. medRxiv July 28 2020
Molecular mechanisms of Cardiac Injury associated with myocardial SARS-CoV-2 infection
Liu, Xian Fang et al. bioRxiv July 27 2020
Automated Fast-Flow Synthesis of Antisense Phosphorodiamidate Morpholino Oligomers
Li, Chengxi et al. ChemRxiv July 22 2020
SARS-CoV-2 and Dengue Virus Coinfection in An Adult with Heterozygous Beta Thalassemia: A Case Report from Bangladesh with Literature Review
Hossain, Md Rezaul et al. SSRN July 15 2020
Outpatient treatment of COVID-19 with steroids in the phase of mild pneumonia without the need for admission as an opportunity to modify the course of the disease: A structured summary of a randomised controlled trial.
Saiz-Rodríguez Miriam, et al. Trials 2020 0 0. (1) 632
Genomic modeling as an approach to identify surrogates for use in experimental validation of SARS-CoV-2 and HuNoVs inactivation by UV-C treatment
Pendyala, Brahmaiah et al. bioRxiv June 16 2020
Proactive Prophylaxis With Azithromycin and HydroxyChloroquine in Hospitalised Patients With COVID-19 (ProPAC-COVID): A structured summary of a study protocol for a randomised controlled trial.
Sivapalan Pradeesh, et al. Trials 2020 0 0. (1) 513
The SARS-CoV-2 Ivermectin Navarra-ISGlobal Trial (SAINT) to Evaluate the Potential of Ivermectin to Reduce COVID-19 Transmission in low risk, non-severe COVID-19 patients in the first 48 hours after symptoms onset: A structured summary of a study protocol for a randomized control pilot trial.
Chaccour Carlos, et al. Trials 2020 0 0. (1) 498
Norwegian Coronavirus Disease 2019 (NO COVID-19) Pragmatic Open label Study to assess early use of hydroxychloroquine sulphate in moderately severe hospitalised patients with coronavirus disease 2019: A structured summary of a study protocol for a randomised controlled trial.
Lyngbakken Magnus Nakrem, et al. Trials 2020 0 0. (1) 485
Controlled, double-blind, randomized trial to assess the efficacy and safety of hydroxychloroquine chemoprophylaxis in SARS CoV2 infection in healthcare personnel in the hospital setting: A structured summary of a study protocol for a randomised controlled trial.
Cuadrado-Lavín Antonio, et al. Trials 2020 0 0. (1) 472
AIDCOV: An Interpretable Artificial Intelligence Model for Detection of COVID-19 from Chest Radiography Images
Zokaeinikoo, Maryam et al. medRxiv May 25 2020
Exploratory Study of the Effectiveness of Granulocyte and Monocyte Adsorptive Apheresis Before Initiation of Steroids in Patients with Active Ulcerative Colitis During the COVID-19 Outbreak (EXPECT Study): A Multicenter Prospective Clinical Trial
Kakimoto, Kazuki et al. SSRN May 24 2020
Activation of the SARS-CoV-2 Receptor Ace2 by Cytokines Through Pan JAK-STAT Enhancers
Hennighausen, Lothar et al. SSRN May 22 2020
Development and Validation of Two In-house, Low-Cost SARS-CoV-2 Detection Assays
Alhamlan, Fatimah S et al. medRxiv May 21 2020
REMBRANDT: A high-throughput barcoded sequencing approach for COVID-19 screening
Palmieri, Dario et al. bioRxiv May 17 2020
SARS-CoV-2 transcriptome analysis and molecular cataloguing of immunodominant epitopes for multi-epitope based vaccine design
Kushwaha, Sandeep Kumar et al. bioRxiv May 15 2020
Diagnosis of Coronavirus Disease 2019 (COVID-19) with Structured Latent Multi-View Representation Learning
Kang, Hengyuan et al. arXiv May 06 2020
COVID-DA: Deep Domain Adaptation from Typical Pneumonia to COVID-19
Zhang, Yifan et al. arXiv April 29 2020
'All In': a pragmatic framework for COVID-19 testing and action on a global scale.
Pettit Syril D, et al. EMBO molecular medicine 2020 0 0. (6) e12634
A 16-Year-Old Boy With Cough and Fever in the Era of COVID-19.
Anderson Kelsey R, et al. Pediatrics 2020 0 0. (1)
A 67-Year-Old Woman with Sudden Hearing Loss Associated with SARS-CoV-2 Infection.
Lamounier Pauliana, et al. The American journal of case reports 2020 0 0. e927519
A comprehensive review of the impact of COVID-19 on human reproductive biology, assisted reproduction care and pregnancy: a Canadian perspective.
Madjunkov Mitko, et al. Journal of ovarian research 2020 0 0. (1) 140
A connectivity map-based drug repurposing study and integrative analysis of transcriptomic profiling of SARS-CoV-2 infection.
Mousavi Seyedeh Zahra, et al. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2020 0 0. 104610
An adaptive randomised placebo controlled phase II trial of antivirals for COVID-19 infection (VIRCO): A structured summary of a study protocol for a randomised controlled trial.
McMahon James H, et al. Trials 2020 0 0. (1) 847
Clinical analysis of pregnant women with 2019 novel coronavirus pneumonia.
Chen Siyu, et al. Journal of medical virology 2020 0 0. (9) 1556-1561
Clinical molecular genetics evaluation in women with reproductive failures.
Bilal Mahmood Y, et al. American journal of reproductive immunology (New York, N.Y. : 1989) 2020 0 0. e13313
Could sudden sensorineural hearing loss be the sole manifestation of COVID-19? An investigation into SARS-COV-2 in the etiology of sudden sensorineural hearing loss.
Kilic Osman, et al. International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases 2020 0 0. 208-211
COVID-19 infection in first trimester of pregnancy marked by a liver cytolysis in a woman previously treated by hydroxychloroquine for repeated implantation failure: a case report.
Lamazou F, et al. BMC infectious diseases 2020 0 0. (1) 845
Delay in IVF treatment up to 180 days does not affect pregnancy outcomes in women with diminished ovarian reserve.
Romanski Phillip A, et al. Human reproduction (Oxford, England) 2020 0 0. (7) 1630-1636
Efficacy of a novel SARS-CoV-2 detection kit without RNA extraction and purification.
Fukumoto Tatsuya, et al. International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases 2020 0 0. 16-17
Host-pathogen interaction in COVID-19: Pathogenesis, potential therapeutics and vaccination strategies.
Varghese Praveen Mathews, et al. Immunobiology 2020 0 0. (6) 152008
Is highly expressed ACE 2 in pregnant women "a curse" in times of COVID-19 pandemic?
Dhaundiyal Ankit, et al. Life sciences 2020 0 0. 118676
Is Vertical Transmission of SARS-CoV-2 Infection Possible in Preterm Triplet Pregnancy? A Case Series.
Alwardi Talal Hamood, et al. The Pediatric infectious disease journal 2020 0 0. (12) e456-e458
Maternal and perinatal outcomes of pregnant women with SARS-CoV-2 infection.
, et al. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2020 0 0. (2) 232-241
Maternal health care management during the outbreak of coronavirus disease 2019.
Chen Yu, et al. Journal of medical virology 2020 0 0. (7) 731-739
Post lockdown COVID-19 seroprevalence and circulation at the time of delivery, France.
Mattern Jérémie, et al. PloS one 2020 0 0. (10) e0240782
Pregnancy and COVID-19: pharmacologic considerations.
D'Souza R, et al. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2020 0 0. (2) 195-203
Prognosis of patients with sickle cell disease and COVID-19: a French experience.
Arlet Jean-Benoît, et al. The Lancet. Haematology 2020 0 0. (9) e632-e634
SARS-CoV-2 in the semen: Where does it come from?
Massarotti Claudia, et al. Andrology 2020 0 0. (1) 39-41
SARS-CoV-2 infection of the placenta.
Hosier Hillary, et al. The Journal of clinical investigation 2020 0 0. (9) 4947-4953
Segmenting areas of potential contamination for adaptive robotic disinfection in built environments.
Hu Da, et al. Building and environment 2020 0 0. 107226
Sickle cell trait and the potential risk of severe coronavirus disease 2019-A mini-review.
Kehinde Tawakalitu Abosede, et al. European journal of haematology 2020 0 0. (5) 519-523
Starting a regional collaborative research group for COVID-19 in pregnancy: the Southern Michigan experience.
Bahado-Singh Ray, et al. Journal of perinatal medicine 2020 0 0. (9) 883-891
The 4 D's of Pellagra and Progress.
Williams Adrian C, et al. International journal of tryptophan research : IJTR 2020 0 0. 1178646920910159
The Efficacy of Famotidine in improvement of outcomes in Hospitalized COVID-19 Patients: A structured summary of a study protocol for a randomised controlled trial.
Samimagham Hamid Reza, et al. Trials 2020 0 0. (1) 848
The SARS-CoV-2 receptor ACE2 expression of maternal-fetal interface and fetal organs by single-cell transcriptome study.
Li Mengmeng, et al. PloS one 2020 0 0. (4) e0230295
Universal screening for SARS-CoV-2 before labor admission during Covid-19 pandemic in Madrid.
Herraiz Ignacio, et al. Journal of perinatal medicine 2020 0 0. (9) 981-984
Vaginal delivery report of a healthy neonate born to a convalescent mother with COVID--19.
Xiong Xiali, et al. Journal of medical virology 2020 0 0. (9) 1657-1659
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About RCH PHGKB
Reproductive and Child Health PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to reproductive and child Health...more
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Common RCH Related Topics
- Attention Deficit/Hyperactivity Disorder
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:May 18, 2024
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