Human Genome Epidemiology Literature Finder
Reproductive and Child Health
Records 1 - 30 (of 45 Records) |
Query Trace: Developmental Disabilities[original query] |
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Fragile X analysis of 1112 prenatal samples from 1991 to 2010. Prenatal diagnosis 2011 Oct 31 (10): 925-31. Nolin Sarah L, Glicksman Anne, Ding Xiaohua, Ersalesi Nicole, Brown W Ted, Sherman Stephanie L, Dobkin Ca |
MTHFR 677C->T genotype is associated with folate and homocysteine concentrations in a large, population-based, double-blind trial of folic acid supplementation. The American journal of clinical nutrition 2011 Jun 93 (6): 1365-72. Crider Krista S, Zhu Jiang-Hui, Hao Ling, Yang Quan-He, Yang Thomas P, Gindler Jacqueline, Maneval David R, Quinlivan Eoin P, Li Zhu, Bailey Lynn B, Berry Robert |
Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease. Blood 2012 Nov 120 (18): 3822-8. Bean Christopher J, Boulet Sheree L, Ellingsen Dorothy, Pyle Meredith E, Barron-Casella Emily A, Casella James F, Payne Amanda B, Driggers Jennifer, Trau Heidi A, Yang Genyan, Jones Kimberly, Ofori-Acquah Solomon F, Hooper W Craig, DeBaun Michael |
Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks. Thrombosis research 2012 Dec 130 (6): 942-7. Bean Christopher J, Boulet Sheree L, Ellingsen Dorothy, Trau Heidi, Ghaji Nafisa, Hooper W Craig, Austin Harla |
The WNT2 gene polymorphism associated with speech delay inherent to autism. Research in developmental disabilities 0 33 (5): 1533-40. Lin Ping-I, Chien Yi-Ling, Wu Yu-Yu, Chen Chia-Hsiang, Gau Susan Shur-Fen, Huang Yu-Shu, Liu Shih-Kai, Tsai Wen-Che, Chiu Yen-N |
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia. British journal of haematology 2013 Oct 163 (2): 268-76. Bean Christopher J, Boulet Sheree L, Yang Genyan, Payne Amanda B, Ghaji Nafisa, Pyle Meredith E, Hooper W Craig, Bhatnagar Pallav, Keefer Jeffrey, Barron-Casella Emily A, Casella James F, Debaun Michael |
Catechol-O-methyltransferase Val158Met polymorphism and hyperactivity symptoms in Egyptian children with autism spectrum disorder. Research in developmental disabilities 2013 Jul 34 (7): 2092-7. Karam Rehab A, Rezk Noha A, Abdelrahman Hadeel M, Hassan Tamer H, Mohammad Doaa, Hashim Haitham M, Fattah Nelly R A Abd |
Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles. American journal of medical genetics. Part A 2013 Apr 161A (4): 771-8. Nolin Sarah L, Sah Sachin, Glicksman Anne, Sherman Stephanie L, Allen Emily, Berry-Kravis Elizabeth, Tassone Flora, Yrigollen Carolyn, Cronister Amy, Jodah Marcia, Ersalesi Nicole, Dobkin Carl, Brown W Ted, Shroff Raghav, Latham Gary J, Hadd Andrew |
Recent insights into genotype-phenotype relationships in patients with Rett syndrome using a fine grain scale. Research in developmental disabilities 2014 Nov 35 (11): 2976-86. Fabio Rosa Angela, Colombo Barbara, Russo Silvia, Cogliati Francesca, Masciadri Maura, Foglia Silvia, Antonietti Alessandro, Tavian Danie |
A genomic copy number variant analysis implicates the MBD5 and HNRNPU genes in Chinese children with infantile spasms and expands the clinical spectrum of 2q23.1 deletion. BMC medical genetics 2014 15 (1): 62. Du Xiaonan, An Yu, Yu Lifei, Liu Renchao, Qin Yanrong, Guo Xiaohong, Sun Daokan, Zhou Shuizhen, Wu Bailin, Jiang Yong-Hui, Wang |
Association of dopamine gene variants, emotion dysregulation and ADHD in autism spectrum disorder. Research in developmental disabilities 2014 Jul 35 (7): 1658-65. Gadow Kenneth D, Pinsonneault Julia K, Perlman Greg, Sadee Wolfga |
Association of 5-HT2A receptor gene polymorphisms with gastrointestinal disorders in Egyptian children with autistic disorder. Research in developmental disabilities 2014 Nov 36C 485-490. Abdelrahman Hadeel M, Sherief Laila M, Alghobashy Ashgan A, Abdel Salam Sanaa M, Hashim Haitham M, Abdel Fattah Nelly R, Mohamed Randa |
Association of toll-like receptors polymorphism and intrauterine transmission of cytomegalovirus. PloS one 2017 12 (12): e0189921. Eldar-Yedidia Yifat, Hillel Miriam, Cohen Amitay, Bar-Meir Maskit, Freier-Dror Yossi, Schlesinger Yechi |
Oxytocin receptors (OXTR) and early parental care: An interaction that modulates psychiatric disorders. Research in developmental disabilities 2017 10 82 27-38. Cataldo Ilaria, Azhari Atiqah, Lepri Bruno, Esposito Gianlu |
Parental overcontrol x OPRM1 genotype interaction predicts school-aged children's sympathetic nervous system activation in response to performance challenge. Research in developmental disabilities 2018 Apr . Partington Lindsey C, Borelli Jessica L, Smiley Patricia, Jarvik Ella, Rasmussen Hannah F, Seaman Lauren C, Nurmi Erika |
Interaction between the Opioid Receptor OPRM1 Gene and Mother-Child Language Style Matching Prospectively Predicts Children's Separation Anxiety Disorder Symptoms. Research in developmental disabilities 2018 3 82 120-131. Boparai Sameen, Borelli Jessica L, Partington Lindsey, Smiley Patricia, Jarvik Ella, Rasmussen Hannah F, Seaman Lauren C, Nurmi Erika |
Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis. BMC medical genetics 2018 3 19 (1): 46. Prasad Aparna, Sdano Matthew A, Vanzo Rena J, Mowery-Rushton Patricia A, Serrano Moises A, Hensel Charles H, Wassman E Robe |
Association between single nucleotide polymorphisms in estrogen receptor 1/2 genes and symptomatic severity of autism spectrum disorder. Research in developmental disabilities 2018 Mar . Doi Hirokazu, Fujisawa Takashi X, Iwanaga Ryoichiro, Matsuzaki Junko, Kawasaki Chisato, Tochigi Mamoru, Sasaki Tsukasa, Kato Nobumasa, Shinohara Kazuyu |
Aberrant, autistic, and food-related behaviors in adults with Prader-Willi syndrome. The comparison between young adults and adults. Research in developmental disabilities 2018 1 73 126-134. Ogata Hiroyuki, Ihara Hiroshi, Gito Masao, Sayama Masayuki, Murakami Nobuyuki, Ayabe Tadayuki, Oto Yuji, Nagai Toshiro, Shimoda Kazuta |
Dopamine transporter genotype modulates brain activity during a working memory task in children with ADHD. Research in developmental disabilities 2019 Jul 92 103430. Pineau Guillaume, Villemonteix Thomas, Slama Hichem, Kavec Martin, Balériaux Danielle, Metens Thierry, Baijot Simon, Mary Alison, Ramoz Nicolas, Gorwood Philip, Peigneux Philippe, Massat Isabel |
KCNQ2 related early-onset epileptic encephalopathies in Chinese children. Journal of neurology 2019 6 266 (9): 2224-2232. Fang Zhi-Xu, Zhang Min, Xie Ling-Ling, Jiang Li, Hong Si-Qi, Li Xiu-Juan, Hu Yue, Chen J |
Evaluating the Role of MAST1 as an Intellectual Disability Disease Gene: Identification of a Novel De Novo Variant in a Patient with Developmental Disabilities. Journal of molecular neuroscience : MN 2019 11 70 (3): 320-327. Ben-Mahmoud Afif, Al-Shamsi Aisha M, Ali Bassam R, Al-Gazali Liha |
Associations Among Diurnal Salivary Cortisol Patterns, Medication Use, and Behavioral Phenotype Features in a Community Sample of Rett Syndrome. American journal on intellectual and developmental disabilities 2020 9 125 (5): 353-368. Byiers Breanne J, Payen Ameante, Feyma Timothy, Panoskaltsis-Mortari Angela, Ehrhardt Michael J, Symons Frank |
Application of Chromosome Microarray Analysis in the Investigation of Developmental Disabilities and Congenital Anomalies: Single Center Experience and Review of NRXN3 and NEDD4L Deletions. Molecular syndromology 2020 11 11 (4): 197-206. Çebi Alper Han, Alt?ner ?u |
Is FMR1 CGG Repeat Number Polymorphism Associated With Phenotypic Variation in the General Population? Report From a Cohort of 5,499 Adults. Frontiers in psychiatry 2021 8 12 727085. Hong Jinkuk, DaWalt Leann, Baker Mei Wang, Berry-Kravis Elizabeth M, Mailick Marsha |
Behavioral Inflexibility Across Two Neurogenetic Conditions: Down Syndrome and Fragile X Syndrome. American journal on intellectual and developmental disabilities 2021 8 126 (5): 409-420. Harrop Clare, Dallman Aaron R, Lecavalier Luc, Bodfish James W, Boyd Brian |
A Tiered Genetic Screening Strategy for the Molecular Diagnosis of Intellectual Disability in Chinese Patients. Frontiers in genetics 2021 10 12 669217. Dai Limeng, Zhang Danyan, Wu Zhifeng, Guan Xingying, Ma Mingfu, Li Lianbing, Zhang Yuping, Bai Yun, Guo Ho |
Linked nosocomial COVID-19 outbreak in three facilities for people with intellectual and developmental disabilities due to SARS-CoV-2 variant B.1.1.519 with spike mutation T478K in the Netherlands. BMC infectious diseases 2022 2 22 (1): 139. Gorgels Koen M F, Dingemans Jozef, van der Veer Brian M J W, Hackert Volker, Hensels Audrey Y J, den Heijer Casper D J, van Alphen Lieke B, Savelkoul Paul H M, Hoebe Christian J P |
The first genome-wide association study of internet addiction; Revealed substantial shared risk factors with neurodevelopmental psychiatric disorders.
Research in developmental disabilities 2022 12 133 104393. Haghighatfard Arvin, Ghaderi Amir Hossein, Mostajabi Parmida, Kashfi Seyedeh Sara, Mohabati Somehsarayee Hediyeh, Shahrani Maryam, Mehrasa Mahla, Haghighat Saba, Farhadi Mahdi, Momayez Sefat Maryam, Shiryazdi Atena Alsadat, Ezzati Naghmeh, Qazvini Masoume Ghasemzadeh, Alizadenik Atie, Moghadam Elham Rastega |
Health Effects of Sleep Quality in Premutation Carrier Mothers of Individuals With Fragile X Syndrome. American journal on intellectual and developmental disabilities 2023 4 128 (3): 254-268. Robert S Dembo, Jinkuk Hong, Leann Smith DaWalt, Elizabeth M Berry-Kravis, Marsha R Maili |
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- Page last updated:Apr 22, 2024
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