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Genome-wide association study suggests that variation at the RCOR1 locus is associated with tinnitus in UK Biobank.
Scientific reports 2021 (1): 6470. Wells Helena R R, Abidin Fatin N Zainul, Freidin Maxim B, Williams Frances M K, Dawson Sally |
| The genetic architecture of structural left-right asymmetry of the human brain.
Nature human behaviour 2021 . Sha Zhiqiang, Schijven Dick, Carrion-Castillo Amaia, Joliot Marc, Mazoyer Bernard, Fisher Simon E, Crivello Fabrice, Francks Cly |
| A Genome-wide Association Study for Concussion Risk.
Medicine and science in sports and exercise 2020 (4): 704-711. Kim Stuart K, Roche Megan D, Fredericson Michael, Dragoo Jason L, Horton Brandon H, Avins Andy L, Belanger Heather G, Ioannidis John P A, Abrams Geoffrey |
| The genetic architecture of the human cerebral cortex.
Science (New York, N.Y.) 2020 (6484): . Grasby Katrina L, Jahanshad Neda, Painter Jodie N, Colodro-Conde Lucía, Bralten Janita, Hibar Derrek P, Lind Penelope A, Pizzagalli Fabrizio, Ching Christopher R K, McMahon Mary Agnes B, Shatokhina Natalia, Zsembik Leo C P, Thomopoulos Sophia I, Zhu Alyssa H, Strike Lachlan T, Agartz Ingrid, Alhusaini Saud, Almeida Marcio A A, Alnæs Dag, Amlien Inge K, Andersson Micael, Ard Tyler, Armstrong Nicola J, Ashley-Koch Allison, Atkins Joshua R, Bernard Manon, Brouwer Rachel M, Buimer Elizabeth E L, Bülow Robin, Bürger Christian, Cannon Dara M, Chakravarty Mallar, Chen Qiang, Cheung Joshua W, Couvy-Duchesne Baptiste, Dale Anders M, Dalvie Shareefa, de Araujo Tânia K, de Zubicaray Greig I, de Zwarte Sonja M C, den Braber Anouk, Doan Nhat Trung, Dohm Katharina, Ehrlich Stefan, Engelbrecht Hannah-Ruth, Erk Susanne, Fan Chun Chieh, Fedko Iryna O, Foley Sonya F, Ford Judith M, Fukunaga Masaki, Garrett Melanie E, Ge Tian, Giddaluru Sudheer, Goldman Aaron L, Green Melissa J, Groenewold Nynke A, Grotegerd Dominik, Gurholt Tiril P, Gutman Boris A, Hansell Narelle K, Harris Mathew A, Harrison Marc B, Haswell Courtney C, Hauser Michael, Herms Stefan, Heslenfeld Dirk J, Ho New Fei, Hoehn David, Hoffmann Per, Holleran Laurena, Hoogman Martine, Hottenga Jouke-Jan, Ikeda Masashi, Janowitz Deborah, Jansen Iris E, Jia Tianye, Jockwitz Christiane, Kanai Ryota, Karama Sherif, Kasperaviciute Dalia, Kaufmann Tobias, Kelly Sinead, Kikuchi Masataka, Klein Marieke, Knapp Michael, Knodt Annchen R, Krämer Bernd, Lam Max, Lancaster Thomas M, Lee Phil H, Lett Tristram A, Lewis Lindsay B, Lopes-Cendes Iscia, Luciano Michelle, Macciardi Fabio, Marquand Andre F, Mathias Samuel R, Melzer Tracy R, Milaneschi Yuri, Mirza-Schreiber Nazanin, Moreira Jose C V, Mühleisen Thomas W, Müller-Myhsok Bertram, Najt Pablo, Nakahara Soichiro, Nho Kwangsik, Olde Loohuis Loes M, Orfanos Dimitri Papadopoulos, Pearson John F, Pitcher Toni L, Pütz Benno, Quidé Yann, Ragothaman Anjanibhargavi, Rashid Faisal M, Reay William R, Redlich Ronny, Reinbold Céline S, Repple Jonathan, Richard Geneviève, Riedel Brandalyn C, Risacher Shannon L, Rocha Cristiane S, Mota Nina Roth, Salminen Lauren, Saremi Arvin, Saykin Andrew J, Schlag Fenja, Schmaal Lianne, Schofield Peter R, Secolin Rodrigo, Shapland Chin Yang, Shen Li, Shin Jean, Shumskaya Elena, Sønderby Ida E, Sprooten Emma, Tansey Katherine E, Teumer Alexander, Thalamuthu Anbupalam, Tordesillas-Gutiérrez Diana, Turner Jessica A, Uhlmann Anne, Vallerga Costanza Ludovica, van der Meer Dennis, van Donkelaar Marjolein M J, van Eijk Liza, van Erp Theo G M, van Haren Neeltje E M, van Rooij Daan, van Tol Marie-José, Veldink Jan H, Verhoef Ellen, Walton Esther, Wang Mingyuan, Wang Yunpeng, Wardlaw Joanna M, Wen Wei, Westlye Lars T, Whelan Christopher D, Witt Stephanie H, Wittfeld Katharina, Wolf Christiane, Wolfers Thomas, Wu Jing Qin, Yasuda Clarissa L, Zaremba Dario, Zhang Zuo, Zwiers Marcel P, Artiges Eric, Assareh Amelia A, Ayesa-Arriola Rosa, Belger Aysenil, Brandt Christine L, Brown Gregory G, Cichon Sven, Curran Joanne E, Davies Gareth E, Degenhardt Franziska, Dennis Michelle F, Dietsche Bruno, Djurovic Srdjan, Doherty Colin P, Espiritu Ryan, Garijo Daniel, Gil Yolanda, Gowland Penny A, Green Robert C, Häusler Alexander N, Heindel Walter, Ho Beng-Choon, Hoffmann Wolfgang U, Holsboer Florian, Homuth Georg, Hosten Norbert, Jack Clifford R, Jang MiHyun, Jansen Andreas, Kimbrel Nathan A, Kolskår Knut, Koops Sanne, Krug Axel, Lim Kelvin O, Luykx Jurjen J, Mathalon Daniel H, Mather Karen A, Mattay Venkata S, Matthews Sarah, Mayoral Van Son Jaqueline, McEwen Sarah C, Melle Ingrid, Morris Derek W, Mueller Bryon A, Nauck Matthias, Nordvik Jan E, Nöthen Markus M, O'Leary Daniel S, Opel Nils, Martinot Marie-Laure Paillère, Pike G Bruce, Preda Adrian, Quinlan Erin B, Rasser Paul E, Ratnakar Varun, Reppermund Simone, Steen Vidar M, Tooney Paul A, Torres Fábio R, Veltman Dick J, Voyvodic James T, Whelan Robert, White Tonya, Yamamori Hidenaga, Adams Hieab H H, Bis Joshua C, Debette Stephanie, Decarli Charles, Fornage Myriam, Gudnason Vilmundur, Hofer Edith, Ikram M Arfan, Launer Lenore, Longstreth W T, Lopez Oscar L, Mazoyer Bernard, Mosley Thomas H, Roshchupkin Gennady V, Satizabal Claudia L, Schmidt Reinhold, Seshadri Sudha, Yang Qiong, , , , , , , Alvim Marina K M, Ames David, Anderson Tim J, Andreassen Ole A, Arias-Vasquez Alejandro, Bastin Mark E, Baune Bernhard T, Beckham Jean C, Blangero John, Boomsma Dorret I, Brodaty Henry, Brunner Han G, Buckner Randy L, Buitelaar Jan K, Bustillo Juan R, Cahn Wiepke, Cairns Murray J, Calhoun Vince, Carr Vaughan J, Caseras Xavier, Caspers Svenja, Cavalleri Gianpiero L, Cendes Fernando, Corvin Aiden, Crespo-Facorro Benedicto, Dalrymple-Alford John C, Dannlowski Udo, de Geus Eco J C, Deary Ian J, Delanty Norman, Depondt Chantal, Desrivières Sylvane, Donohoe Gary, Espeseth Thomas, Fernández Guillén, Fisher Simon E, Flor Herta, Forstner Andreas J, Francks Clyde, Franke Barbara, Glahn David C, Gollub Randy L, Grabe Hans J, Gruber Oliver, Håberg Asta K, Hariri Ahmad R, Hartman Catharina A, Hashimoto Ryota, Heinz Andreas, Henskens Frans A, Hillegers Manon H J, Hoekstra Pieter J, Holmes Avram J, Hong L Elliot, Hopkins William D, Hulshoff Pol Hilleke E, Jernigan Terry L, Jönsson Erik G, Kahn René S, Kennedy Martin A, Kircher Tilo T J, Kochunov Peter, Kwok John B J, Le Hellard Stephanie, Loughland Carmel M, Martin Nicholas G, Martinot Jean-Luc, McDonald Colm, McMahon Katie L, Meyer-Lindenberg Andreas, Michie Patricia T, Morey Rajendra A, Mowry Bryan, Nyberg Lars, Oosterlaan Jaap, Ophoff Roel A, Pantelis Christos, Paus Tomas, Pausova Zdenka, Penninx Brenda W J H, Polderman Tinca J C, Posthuma Danielle, Rietschel Marcella, Roffman Joshua L, Rowland Laura M, Sachdev Perminder S, Sämann Philipp G, Schall Ulrich, Schumann Gunter, Scott Rodney J, Sim Kang, Sisodiya Sanjay M, Smoller Jordan W, Sommer Iris E, St Pourcain Beate, Stein Dan J, Toga Arthur W, Trollor Julian N, Van der Wee Nic J A, van 't Ent Dennis, Völzke Henry, Walter Henrik, Weber Bernd, Weinberger Daniel R, Wright Margaret J, Zhou Juan, Stein Jason L, Thompson Paul M, Medland Sarah E, |
| Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew.
Cerebral cortex (New York, N.Y. : 1991) 2021 . Kong Xiang-Zhen, Postema Merel, Schijven Dick, Castillo Amaia Carrión, Pepe Antonietta, Crivello Fabrice, Joliot Marc, Mazoyer Bernard, Fisher Simon E, Francks Cly |
| Clinical and Genome-Wide Analysis of Multiple Severe Cisplatin-Induced Neurotoxicities in Adult-Onset Cancer Survivors.
Clinical cancer research : an official journal of the American Association for Cancer Research 2020 (24): 6550-6558. Trendowski Matthew R, Wheeler Heather E, El-Charif Omar, Feldman Darren R, Hamilton Robert J, Vaughn David J, Fung Chunkit, Kollmannsberger Christian, Einhorn Lawrence H, Travis Lois B, Dolan M Eile |
| Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality.
Human genetics 2021 Mar 140 (3): 529-552. Adewuyi Emmanuel O, Mehta Divya, Sapkota Yadav, , , Auta Asa, Yoshihara Kosuke, Nyegaard Mette, Griffiths Lyn R, Montgomery Grant W, Chasman Daniel I, Nyholt Dale |
| Secondary Genome-Wide Association Study Using Novel Analytical Strategies Disentangle Genetic Components of Cleft Lip and/or Cleft Palate in 1q32.2.
Genes 2020 Oct 11 (11): . Yang Yunju, Suzuki Akiko, Iwata Junichi, Jun G |
| Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study.
BMJ (Clinical research ed.) 2020 May 369 m1203. Richardson Tom G, Sanderson Eleanor, Elsworth Benjamin, Tilling Kate, Davey Smith Geor |
| Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women.
mSystems 2020 Jul 5 (4): . Mehta Supriya D, Nannini Drew R, Otieno Fredrick, Green Stefan J, Agingu Walter, Landay Alan, Zheng Yinan, Hou Lifa |
| Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan.
Nature communications 2020 03 11 (1): 1536. Hollis Ben, Day Felix R, Busch Alexander S, Thompson Deborah J, Soares Ana Luiza G, Timmers Paul R H J, Kwong Alex, Easton Doug F, Joshi Peter K, Timpson Nicholas J, , , Ong Ken K, Perry John R |
| Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women.
Nature communications 2020 11 11 (1): 5976. Steinthorsdottir Valgerdur, McGinnis Ralph, Williams Nicholas O, Stefansdottir Lilja, Thorleifsson Gudmar, Shooter Scott, Fadista João, Sigurdsson Jon K, Auro Kirsi M, Berezina Galina, Borges Maria-Carolina, Bumpstead Suzannah, Bybjerg-Grauholm Jonas, Colgiu Irina, Dolby Vivien A, Dudbridge Frank, Engel Stephanie M, Franklin Christopher S, Frigge Michael L, Frisbaek Yr, Geirsson Reynir T, Geller Frank, Gretarsdottir Solveig, Gudbjartsson Daniel F, Harmon Quaker, Hougaard David Michael, Hegay Tatyana, Helgadottir Anna, Hjartardottir Sigrun, Jääskeläinen Tiina, Johannsdottir Hrefna, Jonsdottir Ingileif, Juliusdottir Thorhildur, Kalsheker Noor, Kasimov Abdumadjit, Kemp John P, Kivinen Katja, Klungsøyr Kari, Lee Wai K, Melbye Mads, Miedzybrodska Zosia, Moffett Ashley, Najmutdinova Dilbar, Nishanova Firuza, Olafsdottir Thorunn, Perola Markus, Pipkin Fiona Broughton, Poston Lucilla, Prescott Gordon, Saevarsdottir Saedis, Salimbayeva Damilya, Scaife Paula Juliet, Skotte Line, Staines-Urias Eleonora, Stefansson Olafur A, Sørensen Karina Meden, Thomsen Liv Cecilie Vestrheim, Tragante Vinicius, Trogstad Lill, Simpson Nigel A B, , , Aripova Tamara, Casas Juan P, Dominiczak Anna F, Walker James J, Thorsteinsdottir Unnur, Iversen Ann-Charlotte, Feenstra Bjarke, Lawlor Deborah A, Boyd Heather Allison, Magnus Per, Laivuori Hannele, Zakhidova Nodira, Svyatova Gulnara, Stefansson Kari, Morgan Lin |
| Genome-wide Association Studies Reveal Novel Locus With Sex-/Therapy-Specific Fracture Risk Effects in Childhood Cancer Survivors.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2020 Dec . Im Cindy, Li Nan, Moon Wonjong, Liu Qi, Morton Lindsay M, Leisenring Wendy M, Howell Rebecca M, Chow Eric J, Sklar Charles A, Wilson Carmen L, Wang Zhaoming, Sapkota Yadav, Chemaitilly Wassim, Ness Kirsten K, Hudson Melissa M, Robison Leslie L, Bhatia Smita, Armstrong Gregory T, Yasui Yuta |
| Genome-Wide Association of Kidney Traits in Hispanics/Latinos Using Dense Imputed Whole-Genome Sequencing Data: The Hispanic Community Health Study/Study of Latinos.
Circulation. Genomic and precision medicine 2020 Aug 13 (4): e002891. Qian Huijun, Kowalski Madeline H, Kramer Holly J, Tao Ran, Lash James P, Stilp Adrienne M, Cai Jianwen, Li Yun, Franceschini No |
| Risk Y-haplotypes and pathogenic variants of Arab-ancestry boys with autism by an exome-wide association study.
Molecular biology reports 2020 Oct 47 (10): 7623-7632. Alsubaie Laila M, Alsuwat Hind Saleh, Almandil Noor B, AlSulaiman Abdulla, AbdulAzeez Sayed, Borgio J Franc |
| Common variation at 16p11.2 is associated with glycosuria in pregnancy: findings from a genome-wide association study in European women.
Human molecular genetics 2020 Jul 29 (12): 2098-2106. Lee Matthew A, McMahon George, Karhunen Ville, Wade Kaitlin H, Corbin Laura J, Hughes David A, Smith George Davey, Lawlor Debbie A, Jarvelin Marjo-Riitta, Timpson Nicholas |
| Multi-trait analysis for genome-wide association study of five psychiatric disorders.
Translational psychiatry 2020 06 10 (1): 209. Wu Yulu, Cao Hongbao, Baranova Ancha, Huang Hailiang, Li Sheng, Cai Lei, Rao Shuquan, Dai Minhan, Xie Min, Dou Yikai, Hao Qinjian, Zhu Ling, Zhang Xiangrong, Yao Yin, Zhang Fuquan, Xu Mingqing, Wang Qia |
| Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism.
Translational psychiatry 2020 08 10 (1): 265. Matoba Nana, Liang Dan, Sun Huaigu, Aygün Nil, McAfee Jessica C, Davis Jessica E, Raffield Laura M, Qian Huijun, Piven Joseph, Li Yun, Kosuri Sriam, Won Hyejung, Stein Jason |
| Metabolomic and genetic associations with insulin resistance in pregnancy.
Diabetologia 2020 Sep 63 (9): 1783-1795. Liu Yu, Kuang Alan, Talbot Octavious, Bain James R, Muehlbauer Michael J, Hayes M Geoffrey, Ilkayeva Olga R, Lowe Lynn P, Metzger Boyd E, Newgard Christopher B, Scholtens Denise M, Lowe William L, |
| Genome-wide Association Analysis of Proinflammatory Cytokines and Gene-lifestyle Interaction for Invasive Breast Cancer Risk: The WHI dbGaP Study.
Cancer prevention research (Philadelphia, Pa.) 2020 Sep . Jung Su Yon, Scott Peter A, Papp Jeanette C, Sobel Eric M, Pellegrini Matteo, Yu Herbert, Han Sihao, Zhang Zuo-Fe |
| Single nucleotide polymorphism heritability and differential patterns of genetic overlap between inattention and four neurocognitive factors in youth.
Development and psychopathology 2020 Jan 1-11. Micalizzi Lauren, Brick Leslie A, Marraccini Marisa E, Benca-Bachman Chelsie E, Palmer Rohan H C, Knopik Valerie |
| Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.
Communications biology 2020 Mar 3 (1): 129. Olafsdottir Thorhildur, Thorleifsson Gudmar, Sulem Patrick, Stefansson Olafur A, Medek Helga, Olafsson Karl, Ingthorsson Orri, Gudmundsson Valur, Jonsdottir Ingileif, Halldorsson Gisli H, Kristjansson Ragnar P, Frigge Michael L, Stefansdottir Lilja, Sigurdsson Jon K, Oddsson Asmundur, Sigurdsson Asgeir, Eggertsson Hannes P, Melsted Pall, Halldorsson Bjarni V, Lund Sigrun H, Styrkarsdottir Unnur, Steinthorsdottir Valgerdur, Gudmundsson Julius, Holm Hilma, Tragante Vinicius, Asselbergs Folkert W, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Jonsdottir Kristin, Rafnar Thorunn, Stefansson Ka |
| Genetic Contributions to Maternal and Neonatal Vitamin D Levels.
Genetics 2020 Apr 214 (4): 1091-1102. Traglia Michela, Windham Gayle C, Pearl Michelle, Poon Victor, Eyles Darryl, Jones Karen L, Lyall Kristen, Kharrazi Martin, Croen Lisa A, Weiss Lauren |
| Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
Translational psychiatry 2020 Jul 10 (1): 215. Yousaf Afsheen, Waltes Regina, Haslinger Denise, Klauck Sabine M, Duketis Eftichia, Sachse Michael, Voran Anette, Biscaldi Monica, Schulte-Rüther Martin, Cichon Sven, Nöthen Markus, Ackermann Jörg, Koch Ina, Freitag Christine M, Chiocchetti Andreas |
| Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths.
Soa--ch'ongsonyon chongsin uihak = Journal of child & adolescent psychiatry 2018 Apr 29 (2): 62-72. Kweon Kukju, Shin Eun-Soon, Park Kee Jeong, Lee Jong-Keuk, Joo Yeonho, Kim Hyo-W |
| A genome-wide association study of polycystic ovary syndrome identified from electronic health records.
American journal of obstetrics and gynecology 2020 Apr . Zhang Yanfei, Ho Kevin, Keaton Jacob M, Hartzel Dustin N, Day Felix, Justice Anne E, Josyula Navya S, Pendergrass Sarah A, Actkins Ky'Era, Davis Lea K, Velez Edwards Digna R, Holohan Brody, Ramirez Andrea, Stanaway Ian B, Crosslin David R, Jarvik Gail P, Sleiman Patrick, Hakonarson Hakon, Williams Marc S, Michael Lee Ming |
| Shared genetic background between children and adults with attention deficit/hyperactivity disorder.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2020 Apr . Rovira Paula, Demontis Ditte, Sánchez-Mora Cristina, Zayats Tetyana, Klein Marieke, Mota Nina Roth, Weber Heike, Garcia-Martínez Iris, Pagerols Mireia, Vilar Laura, Arribas Lorena, Richarte Vanesa, Corrales Montserrat, Fadeuilhe Christian, Bosch Rosa, Martin Gemma Español, Almos Peter, Doyle Alysa E, Grevet Eugenio Horacio, Grimm Oliver, Halmøy Anne, Hoogman Martine, Hutz Mara, Jacob Christian P, Kittel-Schneider Sarah, Knappskog Per M, Lundervold Astri J, Rivero Olga, Rovaris Diego Luiz, Salatino-Oliveira Angelica, da Silva Bruna Santos, Svirin Evgeniy, Sprooten Emma, Strekalova Tatyana, , , Arias-Vasquez Alejandro, Sonuga-Barke Edmund J S, Asherson Philip, Bau Claiton Henrique Dotto, Buitelaar Jan K, Cormand Bru, Faraone Stephen V, Haavik Jan, Johansson Stefan E, Kuntsi Jonna, Larsson Henrik, Lesch Klaus-Peter, Reif Andreas, Rohde Luis Augusto, Casas Miquel, Børglum Anders D, Franke Barbara, Ramos-Quiroga Josep Antoni, Artigas María Soler, Ribasés Mar |
| A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness.
Human genetics 2020 Mar . Nudel Ron, Appadurai Vivek, Schork Andrew J, Buil Alfonso, Bybjerg-Grauholm Jonas, Børglum Anders D, Daly Mark J, Mors Ole, Hougaard David M, Mortensen Preben Bo, Werge Thomas, Nordentoft Merete, Thompson Wesley K, Benros Michael |
| Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity.
Genes 2020 Feb 11 (3): . Adewuyi Emmanuel O, Sapkota Yadav, International Endogene Consortium Iec , andMe Research Team , International Headache Genetics Consortium Ihgc , Auta Asa, Yoshihara Kosuke, Nyegaard Mette, Griffiths Lyn R, Montgomery Grant W, Chasman Daniel I, Nyholt Dale |
| Genome-wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders.
Genes, brain, and behavior 2020 Feb e12648. Price Kaitlyn M, Wigg Karen G, Feng Yu, Blokland Kirsten, Wilkinson Margaret, He Gengming, Kerr Elizabeth N, Carter Tasha-Cate, Guger Sharon L, Lovett Maureen W, Strug Lisa J, Barr Cathy |
| Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment.
Cortex; a journal devoted to the study of the nervous system and behavior 2019 Nov 124 137-153. Carrion-Castillo Amaia, Pepe Antonietta, Kong Xiang-Zhen, Fisher Simon E, Mazoyer Bernard, Tzourio-Mazoyer Nathalie, Crivello Fabrice, Francks Cly |
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- Page last updated:Oct 20, 2021
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