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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
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Last data update: Apr 23, 2024
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Anemia[original query]>>Original Studies[Product Type]
Prevalence of common autosomal recessive mutation carriers in women in the Southern Vietnam following the application of expanded carrier screening.
Xuan-Hong To-Mai et al. Sci Rep 2024 14(1) 7461
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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
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Two-Dimensional Ultrasound Assessment of Long-Term Intra-Abdominal Organ Changes in Children with Sickle Cell Anemia during Steady State: A Comparative Study.
C S Nwosu et al. Niger J Clin Pract 2023 26(12) 1861-1867
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Newborn screening for sickle cell anemia in Antalya, Türkiye.
Zeynep Öztürk et al. Turk J Pediatr 2024 65(6) 959-963
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Comparing Active Surveillance and Watchful Waiting With Radical Treatment Using Machine Learning Models Among Patients With Prostate Cancer.
Siqi Hu et al. JCO Clin Cancer Inform 2023 7e2300083
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A Newborn Screening Program for Sickle Cell Disease in Murcia (Spain).
María Sánchez-Villalobos et al. Int J Neonatal Screen 2023 9(4)
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Identifying patients at risk for hereditary myeloid malignancy syndromes incorporating a novel, self-administered questionnaire to an initial screening platform.
Mohammad Faizan Zahid et al. Eur J Haematol 2023
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Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome.
Dervla M Connaughton et al. J Mol Med (Berl) 2023
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Food Consumption of People with Sickle Cell Anemia in a Middle-Income Country.
Tamara Vilhena Teixeira et al. Nutrients 2023 15(6)
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Iron Status in Sickle Cell Anemia: Deficiency or Overload?
Varsha P Patel et al. Cureus 2023 15(2) e35310
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Development and validation of machine learning models for postoperative venous thromboembolism prediction in colorectal cancer inpatients: a retrospective study.
Li Qin et al. Journal of gastrointestinal oncology 2023 14(1) 220-232
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Predicting Pain in People With Sickle Cell Disease in the Day Hospital Using the Commercial Wearable Apple Watch: Feasibility Study.
Rebecca Sofia Stojancic et al. JMIR formative research 2023 7e45355
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Evaluation of Alisertib Alone or Combined With Fulvestrant in Patients With Endocrine-Resistant Advanced Breast Cancer: The Phase 2 TBCRC041 Randomized Clinical Trial.
Tufia C Haddad et al. JAMA oncology 2023
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Effectiveness of intermittent screening and treatment of malaria in pregnancy on maternal and birth outcomes in selected districts in Rwanda: A cluster randomized controlled trial.
Aline Uwimana et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2023
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Genomic Analyses of Germline and Somatic Variation in High-Grade Serous Ovarian Cancer.
Aaron W Adamson et al. Research square 2023
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Five Years' Experience with Gene Panel Sequencing in Hereditary Hemolytic Anemia Screened by Routine Peripheral Blood Smear Examination.
Namsu Kim et al. Diagnostics (Basel, Switzerland) 2023 13(4)
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Clinical Utility of Targeted Next-Generation Sequencing Panel in Routine Diagnosis of Hereditary Hemolytic Anemia: A national reference laboratory experience.
Archana M Agarwal et al. European journal of haematology 2023
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Functional interpretation, cataloging, and analysis of 1,341 glucose-6-phosphate dehydrogenase variants.
Geck Renee C et al. American journal of human genetics 2023
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Basic biochemical and hematological parameters of structural hemoglobin variants in the postpartum women and their respective newborn from Manaus, Amazonas, Brazil.
da Silva Brito Roberta et al. BMC pregnancy and childbirth 2022 22(1) 936
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A non-invasive machine learning mechanism for early disease recognition on Twitter: The case of anemia.
Sarsam Samer Muthana et al. Artificial intelligence in medicine 2022 134102428
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Prediction of anemia using facial images and deep learning technology in the emergency department.
Zhang Aixian et al. Frontiers in public health 2022 10964385
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Cobimetinib Plus Vemurafenib in Patients With Colorectal Cancer With BRAF Mutations: Results From the Targeted Agent and Profiling Utilization Registry (TAPUR) Study.
Klute Kelsey A et al. JCO precision oncology 2022 6e2200191
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Creating an Automated Contemporaneous Cohort in Sickle Cell Anemia to Predict Survival After Disease-Modifying Therapy.
Cronin Robert M et al. Blood advances 2022
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Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia.
Ranza Emmanuelle et al. American journal of medical genetics. Part A 2022
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ASSESSING PATIENT ATTITUDES TOWARD GENETIC TESTING FOR HEREDITARY HEMATOLOGIC MALIGNANCY.
Johnson Addison Q et al. European journal of haematology 2022
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Surveillance for Sickle Cell Disease - Sickle Cell Data Collection Program, Two States, 2004-2018.
Snyder Angela B et al. Morbidity and mortality weekly report. Surveillance summaries (Washington, D.C. : 2002) 2022 71(9) 1-18
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Newborn screening for propionic, methylmalonic acidemia and vitamin B12 deficiency. Analysis of 588,793 newborns.
Martín-Rivada Álvaro et al. Journal of pediatric endocrinology & metabolism : JPEM 2022
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Vital Signs: Use of Recommended Health Care Measures to Prevent Selected Complications of Sickle Cell Anemia in Children and Adolescents — Selected U.S. States, 2019
LA Schieve et al, CDC, MMWR, September 20, 2022
Stroke Prevention with Hydroxyurea Enabled through Research and Education (SPHERE): a Phase 2 primary stroke prevention trial in sub-Saharan Africa.
Smart Luke R et al. Acta haematologica 2022
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Phase II Study of Afatinib in Patients With Tumors With Human Epidermal Growth Factor Receptor 2-Activating Mutations: Results From the National Cancer Institute-Molecular Analysis for Therapy Choice ECOG-ACRIN Trial (EAY131) Subprotocol EAY131-B.
Bedard Philippe L et al. JCO precision oncology 2022 6e2200165
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 23, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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