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Reproductive and Child Health
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Shared genetics between autism spectrum disorder and attention-deficit/hyperactivity disorder and their association with extraversion.
Psychiatry research 2022 6 314 114679. Baranova Ancha, Wang Jun, Cao Hongbao, Chen Jiang-Huan, Chen Jiu, Chen Miao, Ni Sulin, Xu Xijia, Ke Xiaoyan, Xie Shiping, Sun Jing, Zhang Fuqu |
| Maternal selenium levels and whole genome screen in recurrent spontaneous preterm birth population: A nested case control study.
European journal of obstetrics, gynecology, and reproductive biology 2021 9 265 203-211. Care Angharad G, Gupta Juhi K, Goodfellow Laura, Zhang Ge, Monangi Nagendra, Belling Elizabeth, Landero Julio, Chappell Joanne, Sharp Andrew, Alfirevic Ana, Müller-Myhsok Bertram, Muglia Louis J, Alfirevic Zar |
| Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes.
American journal of human genetics 2022 5 109 (6): 1117-1139. Nieves-Colón Maria A, Badillo Rivera Keyla M, Sandoval Karla, Villanueva Dávalos Vanessa, Enriquez Lencinas Luis E, Mendoza-Revilla Javier, Adhikari Kaustubh, González-Buenfil Ram, Chen Jessica W, Zhang Elisa T, Sockell Alexandra, Ortiz-Tello Patricia, Hurtado Gloria Malena, Condori Salas Ramiro, Cebrecos Ricardo, Manzaneda Choque José C, Manzaneda Choque Franz P, Yábar Pilco Germán P, Rawls Erin, Eng Celeste, Huntsman Scott, Burchard Esteban, Ruiz-Linares Andrés, González-José Rolando, Bedoya Gabriel, Rothhammer Francisco, Bortolini Maria Cátira, Poletti Giovanni, Gallo Carla, Bustamante Carlos D, Baker Julie C, Gignoux Christopher R, Wojcik Genevieve L, Moreno-Estrada Andr |
| Genome-wide association study meta-analysis identifies three novel loci for circulating anti-Müllerian hormone levels in women.
Human reproduction (Oxford, England) 2022 3 37 (5): 1069-1082. Verdiesen Renée M G, van der Schouw Yvonne T, van Gils Carla H, Verschuren W M Monique, Broekmans Frank J M, Borges Maria C, Gonçalves Soares Ana L, Lawlor Deborah A, Eliassen A Heather, Kraft Peter, Sandler Dale P, Harlow Siobán D, Smith Jennifer A, Santoro Nanette, Schoemaker Minouk J, Swerdlow Anthony J, Murray Anna, Ruth Katherine S, Onland-Moret N Charlot |
| GWAS on birth year infant mortality rates provides evidence of recent natural selection.
Proceedings of the National Academy of Sciences of the United States of America 2022 3 119 (12): e2117312119. Wu Yuchang, Furuya Shiro, Wang Zihang, Nobles Jenna E, Fletcher Jason M, Lu Qiongs |
| Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder.
Nature genetics 2022 8 54 (8): 1117-1124. Rajagopal Veera M, Duan Jinjie, Vilar-Ribó Laura, Grove Jakob, Zayats Tetyana, Ramos-Quiroga J Antoni, Satterstrom F Kyle, Artigas María Soler, Bybjerg-Grauholm Jonas, Bækvad-Hansen Marie, Als Thomas D, Rosengren Anders, Daly Mark J, Neale Benjamin M, Nordentoft Merete, Werge Thomas, Mors Ole, Hougaard David M, Mortensen Preben B, Ribasés Marta, Børglum Anders D, Demontis Dit |
| A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study.
American journal of medical genetics. Part A 2022 4 188 (8): 2303-2314. Rashkin Sara R, Cleves Mario, Shaw Gary M, Nembhard Wendy N, Nestoridi Eirini, Jenkins Mary M, Romitti Paul A, Lou Xiang-Yang, Browne Marilyn L, Mitchell Laura E, Olshan Andrew F, Lomangino Kevin, Bhattacharyya Sudeepa, Witte John S, Hobbs Charlotte A, |
| Genome-wide Interaction Study Implicates
Frontiers in cell and developmental biology 2022 3 10 621261. Carlson Jenna C, Shaffer John R, Deleyiannis Fred, Hecht Jacqueline T, Wehby George L, Christensen Kaare, Feingold Eleanor, Weinberg Seth M, Marazita Mary L, Leslie Elizabeth |
| Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways.
Human reproduction (Oxford, England) 2022 4 37 (2): 366-383. Adewuyi E O, Mehta D, , , Nyholt D |
| Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer.
Genome medicine 2022 3 14 (1): 32. Dong Qian, Song Nan, Qin Na, Chen Cheng, Li Zhenghong, Sun Xiaojun, Easton John, Mulder Heather, Plyler Emily, Neale Geoffrey, Walker Emily, Li Qian, Ma Xiaotu, Chen Xiang, Huang I-Chan, Yasui Yutaka, Ness Kirsten K, Zhang Jinghui, Hudson Melissa M, Robison Leslie L, Wang Zhaomi |
| Association of Single-Nucleotide Variants in the Human Leukocyte Antigen and Other Loci With Childhood Hodgkin Lymphoma.
JAMA network open 2022 08 5 (8): e2225647. Chen Cheng, Song Nan, Dong Qian, Sun Xiaojun, Mulder Heather L, Easton John, Zhang Jinghui, Yasui Yutaka, Bhatia Smita, Armstrong Gregory T, Wang Hui, Ness Kirsten K, Hudson Melissa M, Robison Leslie L, Wang Zhaomi |
| Polygenic risk scores and the need for pharmacotherapy in neonatal abstinence syndrome.
Pediatric research 2022 Aug . Bibi Shawana, Gaddis Nathan, Johnson Eric O, Lester Barry M, Kraft Walter, Singh Rachana, Terrin Norma, Adeniyi-Jones Susan, Davis Jonathan |
| GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements.
Nature communications 2022 08 13 (1): 4840. Dixon Peter H, Levine Adam P, Cebola Inês, Chan Melanie M Y, Amin Aliya S, Aich Anshul, Mozere Monika, Maude Hannah, Mitchell Alice L, Zhang Jun, , , Chambers Jenny, Syngelaki Argyro, Donnelly Jennifer, Cooley Sharon, Geary Michael, Nicolaides Kypros, Thorsell Malin, Hague William M, Estiu Maria Cecilia, Marschall Hanns-Ulrich, Gale Daniel P, Williamson Catheri |
| Population-scale analysis of common and rare genetic variation associated with hearing loss in adults.
Communications biology 2022 06 5 (1): 540. Praveen Kavita, Dobbyn Lee, Gurski Lauren, Ayer Ariane H, Staples Jeffrey, Mishra Shawn, Bai Yu, Kaufman Alexandra, Moscati Arden, Benner Christian, Chen Esteban, Chen Siying, Popov Alexander, Smith Janell, , , , Melander Olle, Jones Marcus B, Marchini Jonathan, Balasubramanian Suganthi, Zambrowicz Brian, Drummond Meghan C, Baras Aris, Abecasis Goncalo R, Ferreira Manuel A, Stahl Eli A, Coppola Giovan |
| Genome-Wide Admixture Mapping of Estimated Glomerular Filtration Rate and Chronic Kidney Disease Identifies European and African Ancestry-of-Origin Loci in Hispanic and Latino Individuals in the United States.
Journal of the American Society of Nephrology : JASN 2021 10 33 (1): 77-87. Horimoto Andrea R V R, Xue Diane, Cai Jianwen, Lash James P, Daviglus Martha L, Franceschini Nora, Thornton Timothy |
| Platelet response to aspirin in UK and Irish pregnancy cohorts: a genome-wide approach.
Platelets 2021 12 1-7. Mone Fionnuala, Gupta Juhi K, Phelan Marie M, Meher Shireen, Lian Lu Yung, Francis Ben, Zhang Eunice, Mulcahy Cecilia, Alfirevic Ana, Mcauliffe Fionnuala M, Navaratnam Ka |
| Shared genetic influences on depression and menopause symptoms.
Psychological medicine 2021 12 1-11. Meijsen Joeri J, Shen Hanyang, Vemuri Mytilee, Rasgon Natalie L, Koenen Karestan C, Duncan Laramie |
| Integration of Transcriptome and Exome Genotyping Identifies Significant Variants with Autism Spectrum Disorder.
Pharmaceuticals (Basel, Switzerland) 2022 Jan 15 (2): . Almandil Noor B, AlSulaiman Abdulla, Aldakeel Sumayh A, Alkuroud Deem N, Aljofi Halah Egal, Alzahrani Safah, Al-Mana Aishah, Alfuraih Asma A, Alabdali Majed, Alkhamis Fahd A, AbdulAzeez Sayed, Borgio J Franc |
| Genetic Link Determining the Maternal-Fetal Circulation of Vitamin D.
Frontiers in genetics 2021 10 12 721488. Sampathkumar Aparna, Tan Karen M, Chen Li, Chong Mary F F, Yap Fabian, Godfrey Keith M, Chong Yap Seng, Gluckman Peter D, Ramasamy Adaikalavan, Karnani Neer |
| Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia.
American journal of human genetics 2021 9 108 (10): 1823-1835. Kachuri Linda, Jeon Soyoung, DeWan Andrew T, Metayer Catherine, Ma Xiaomei, Witte John S, Chiang Charleston W K, Wiemels Joseph L, de Smith Adam |
| Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
PLoS genetics 2021 7 17 (7): e1009584. Ray Debashree, Venkataraghavan Sowmya, Zhang Wanying, Leslie Elizabeth J, Hetmanski Jacqueline B, Weinberg Seth M, Murray Jeffrey C, Marazita Mary L, Ruczinski Ingo, Taub Margaret A, Beaty Terri |
| Role of Sex on the Genetic Susceptibility to Childhood Asthma in Latinos and African Americans.
Journal of personalized medicine 2021 Nov 11 (11): . Espuela-Ortiz Antonio, Herrera-Luis Esther, Lorenzo-Díaz Fabián, Hu Donglei, Eng Celeste, Villar Jesús, Rodriguez-Santana Jose R, Burchard Esteban G, Pino-Yanes Mar |
| Interaction of Polygenetic Variants for Gestational Diabetes Mellitus Risk with Breastfeeding and Korean Balanced Diet to Influence Type 2 Diabetes Risk in Later Life in a Large Hospital-Based Cohort.
Journal of personalized medicine 2021 Nov 11 (11): . Park Sunm |
| Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour.
Nature human behaviour 2021 7 . Mills Melinda C, Tropf Felix C, Brazel David M, van Zuydam Natalie, Vaez Ahmad, , , , Pers Tune H, Snieder Harold, Perry John R B, Ong Ken K, den Hoed Marcel, Barban Nicola, Day Felix |
| TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study.
NPJ precision oncology 2021 7 5 (1): 64. Meijer A J M, Diepstraten F A, Langer T, Broer L, Domingo I K, Clemens E, Uitterlinden A G, de Vries A C H, van Grotel M, Vermeij W P, Ozinga R A, Binder H, Byrne J, van Dulmen-den Broeder E, Garrè M L, Grabow D, Kaatsch P, Kaiser M, Kenborg L, Winther J F, Rechnitzer C, Hasle H, Kepak T, Kepakova K, Tissing W J E, van der Kooi A L F, Kremer L C M, Kruseova J, Pluijm S M F, Kuehni C E, van der Pal H J H, Parfitt R, Spix C, Tillmanns A, Deuster D, Matulat P, Calaminus G, Hoetink A E, Elsner S, Gebauer J, Haupt R, Lackner H, Blattmann C, Neggers S J C M M, Rassekh S R, Wright G E B, Brooks B, Nagtegaal A P, Drögemöller B I, Ross C J D, Bhavsar A P, Am Zehnhoff-Dinnesen A G, Carleton B C, Zolk O, van den Heuvel-Eibrink M M, , |
| Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction.
Nature neuroscience 2021 8 24 (10): 1367-1376. Karlsson Linnér Richard, Mallard Travis T, Barr Peter B, Sanchez-Roige Sandra, Madole James W, Driver Morgan N, Poore Holly E, de Vlaming Ronald, Grotzinger Andrew D, Tielbeek Jorim J, Johnson Emma C, Liu Mengzhen, Rosenthal Sara Brin, Ideker Trey, Zhou Hang, Kember Rachel L, Pasman Joëlle A, Verweij Karin J H, Liu Dajiang J, Vrieze Scott, , Kranzler Henry R, Gelernter Joel, Harris Kathleen Mullan, Tucker-Drob Elliot M, Waldman Irwin D, Palmer Abraham A, Harden K Paige, Koellinger Philipp D, Dick Danielle |
| Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort.
NeuroImage. Clinical 2021 Sep 32 102823. Zainul Abidin Fatin N, Scelsi Marzia A, Dawson Sally J, Altmann Andre, |
| Host Genetic Risk Factors for Chlamydia trachomatis-Related Infertility in Women.
The Journal of infectious diseases 2021 Aug 224 (Supplement_2): S64-S71. Zheng Xiaojing, Zhong Wujuan, O'Connell Catherine M, Liu Yutong, Haggerty Catherine L, Geisler William M, Anyalechi Gloria E, Kirkcaldy Robert D, Wiesenfeld Harold C, Hillier Sharon L, Steinkampf Michael P, Hammond Karen R, Fine Jason, Li Yun, Darville To |
| Genetic factors of idiopathic central precocious puberty and their polygenic risk in early puberty.
European journal of endocrinology 2021 Jul . Lin Wei-De, Cheng Chi-Fung, Wang Chung-Hsing, Liang Wen-Miin, Chen Chien-Hsiun, Hsieh Ai-Ru, Chiu Mu-Lin, Lin Ting-Hsu, Liao Chiu-Chu, Huang Shao-Mei, Tsai Chang-Hai, Chang Cherry Yin-Yi, Lin Ying-Ju, Tsai Fuu-J |
| Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci.
Communications biology 2021 Jul 4 (1): 908. Qu Hui-Qi, Qu Jingchun, Bradfield Jonathan, Marchand Luc, Glessner Joseph, Chang Xiao, March Michael, Li Jin, Connolly John J, Roizen Jeffrey D, Sleiman Patrick, Polychronakos Constantin, Hakonarson Hak |
| Genetic, Clinical, and Sociodemographic Factors Associated With Stimulant Treatment Outcomes in ADHD.
The American journal of psychiatry 2021 Jun appiajp202020121686. Brikell Isabell, Wimberley Theresa, Albiñana Clara, Pedersen Emil Michael, Vilhjálmsson Bjarni Jóhann, Agerbo Esben, Demontis Ditte, Børglum Anders D, Schork Andrew J, LaBianca Sonja, Werge Thomas, Mors Ole, Hougaard David M, Thapar Anita, Mortensen Preben Bo, Dalsgaard Sør |
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- Page last updated:Feb 07, 2023
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