Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: Data sharing[original query] |
---|
Folic acid supplementation use and the MTHFR C677T polymorphism in orofacial clefts etiology: An individual participant data pooled-analysis. Birth defects research. Part A, Clinical and molecular teratology 2013 Aug 97 (8): 509-14. Butali Azeez, Little Julian, Chevrier Cécile, Cordier Sylvian, Steegers-Theunissen Regine, Jugessur Astanand, Oladugba Bola, Mossey Peter |
The FTO A/T polymorphism and elite athletic performance: a study involving three groups of European athletes. PloS one 2013 8 (4): e60570. Eynon Nir, Nasibulina Emiliya S, Banting Lauren K, Cieszczyk Pawel, Maciejewska-Karlowska Agnieszka, Sawczuk Marek, Bondareva Elvira A, Shagimardanova Roza R, Raz Maytal, Sharon Yael, Williams Alun G, Ahmetov Ildus I, Lucia Alejandro, Birk Ru |
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior genetics 2015 Sep . Schwantes-An Tae-Hwi, Zhang Juan, Chen Li-Shiun, Hartz Sarah M, Culverhouse Robert C, Chen Xiangning, Coon Hilary, Frank Josef, Kamens Helen M, Konte Bettina, Kovanen Leena, Latvala Antti, Legrand Lisa N, Maher Brion S, Melroy Whitney E, Nelson Elliot C, Reid Mark W, Robinson Jason D, Shen Pei-Hong, Yang Bao-Zhu, Andrews Judy A, Aveyard Paul, Beltcheva Olga, Brown Sandra A, Cannon Dale S, Cichon Sven, Corley Robin P, Dahmen Norbert, Degenhardt Louisa, Foroud Tatiana, Gaebel Wolfgang, Giegling Ina, Glatt Stephen J, Grucza Richard A, Hardin Jill, Hartmann Annette M, Heath Andrew C, Herms Stefan, Hodgkinson Colin A, Hoffmann Per, Hops Hyman, Huizinga David, Ising Marcus, Johnson Eric O, Johnstone Elaine, Kaneva Radka P, Kendler Kenneth S, Kiefer Falk, Kranzler Henry R, Krauter Ken S, Levran Orna, Lucae Susanne, Lynskey Michael T, Maier Wolfgang, Mann Karl, Martin Nicholas G, Mattheisen Manuel, Montgomery Grant W, Müller-Myhsok Bertram, Murphy Michael F, Neale Michael C, Nikolov Momchil A, Nishita Denise, Nöthen Markus M, Nurnberger John, Partonen Timo, Pergadia Michele L, Reynolds Maureen, Ridinger Monika, Rose Richard J, Rouvinen-Lagerström Noora, Scherbaum Norbert, Schmäl Christine, Soyka Michael, Stallings Michael C, Steffens Michael, Treutlein Jens, Tsuang Ming, Wall Tamara L, Wodarz Norbert, Yuferov Vadim, Zill Peter, Bergen Andrew W, Chen Jingchun, Cinciripini Paul M, Edenberg Howard J, Ehringer Marissa A, Ferrell Robert E, Gelernter Joel, Goldman David, Hewitt John K, Hopfer Christian J, Iacono William G, Kaprio Jaakko, Kreek Mary Jeanne, Kremensky Ivo M, Madden Pamela A F, McGue Matt, Munafò Marcus R, Philibert Robert A, Rietschel Marcella, Roy Alec, Rujescu Dan, Saarikoski Sirkku T, Swan Gary E, Todorov Alexandre A, Vanyukov Michael M, Weiss Robert B, Bierut Laura J, Saccone Nancy |
Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy. Neurology. Genetics 2016 Dec 2 (6): e118. Møller Rikke S, Weckhuysen Sarah, Chipaux Mathilde, Marsan Elise, Taly Valerie, Bebin E Martina, Hiatt Susan M, Prokop Jeremy W, Bowling Kevin M, Mei Davide, Conti Valerio, de la Grange Pierre, Ferrand-Sorbets Sarah, Dorfmüller Georg, Lambrecq Virginie, Larsen Line H G, Leguern Eric, Guerrini Renzo, Rubboli Guido, Cooper Gregory M, Baulac Stéphan |
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants. CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2018 2 190 (5): E126-E136. Reuter Miriam S, Walker Susan, Thiruvahindrapuram Bhooma, Whitney Joe, Cohn Iris, Sondheimer Neal, Yuen Ryan K C, Trost Brett, Paton Tara A, Pereira Sergio L, Herbrick Jo-Anne, Wintle Richard F, Merico Daniele, Howe Jennifer, MacDonald Jeffrey R, Lu Chao, Nalpathamkalam Thomas, Sung Wilson W L, Wang Zhuozhi, Patel Rohan V, Pellecchia Giovanna, Wei John, Strug Lisa J, Bell Sherilyn, Kellam Barbara, Mahtani Melanie M, Bassett Anne S, Bombard Yvonne, Weksberg Rosanna, Shuman Cheryl, Cohn Ronald D, Stavropoulos Dimitri J, Bowdin Sarah, Hildebrandt Matthew R, Wei Wei, Romm Asli, Pasceri Peter, Ellis James, Ray Peter, Meyn M Stephen, Monfared Nasim, Hosseini S Mohsen, Joseph-George Ann M, Keeley Fred W, Cook Ryan A, Fiume Marc, Lee Hin C, Marshall Christian R, Davies Jill, Hazell Allison, Buchanan Janet A, Szego Michael J, Scherer Stephen |
Frequency of frontotemporal dementia gene variants in C9ORF72, MAPT, and GRN in academic versus commercial laboratory cohorts. Advances in genomics and genetics 2019 4 8 23-33. Steele Natasha Zr, Bright Alison R, Lee Suzee E, Fong Jamie C, Bonham Luke W, Karydas Anna, Karbassi Izabela D, Pribadi Mochtar, Meservey Marc A, Gallen Matthew C, Ramos Eliana Marisa, Liaquat Khalida, Hoffman Carol C, Krasner Meagan R, Dodge Whitney, L Miller Bruce, Coppola Giovanni, Rankin Katherine P, Yokoyama Jennifer S, Higgins Joseph |
Germline Missense Variants in BRCA1: New Trends and Challenges for Clinical Annotation. Cancers 2019 Apr 11 (4): . Golubeva Volha A, Nepomuceno Thales C, Monteiro Alvaro N |
Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience. American journal of medical genetics. Part A 2019 3 179 (6): 927-935. Al-Dewik Nader, Mohd Howaida, Al-Mureikhi Mariam, Ali Rehab, Al-Mesaifri Fatma, Mahmoud Laila, Shahbeck Noora, El-Akouri Karen, Almulla Mariam, Al Sulaiman Reem, Musa Sara, Al-Marri Ajayeb Al-Nabet, Richard Gabriele, Juusola Jane, Solomon Benjamin D, Alkuraya Fowzan S, Ben-Omran Tawf |
SNP-HLA Reference Consortium (SHLARC): HLA and SNP data sharing for promoting MHC-centric analyses in genomics. Genetic epidemiology 2020 7 44 (7): 733-740. Vince Nicolas, Douillard Venceslas, Geffard Estelle, Meyer Diogo, Castelli Erick C, Mack Steven J, Limou Sophie, Gourraud Pierre-Antoi |
Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing? Journal of the American Heart Association 2020 4 9 (8): e015473. Mazzarotto Francesco, Olivotto Iacopo, Boschi Beatrice, Girolami Francesca, Poggesi Corrado, Barton Paul J R, Walsh Rod |
Spectrum of Somatic Cancer Gene Variations Among Adults With Appendiceal Cancer by Age at Disease Onset. JAMA network open 2020 12 3 (12): e2028644. Holowatyj Andreana N, Eng Cathy, Wen Wanqing, Idrees Kamran, Guo Xing |
Detailed Phenotype of GLA Variants Identified by the Nationwide Neurological Screening of Stroke Patients in the Czech Republic. Journal of clinical medicine 2021 8 10 (16): . Reková Petra, Dostálová Gabriela, Kemlink David, Paulasová Schwabová Jaroslava, Dubská Zora, Vaneckova Manuela, Mašek Martin, Kodet Ond?ej, Poup?tová Helena, Mazurová Stella, Rajdova Aneta, Vlckova Eva, Tábo?íková Alena, Fafejtová Št?pánka, Nevsimalova Miroslava, Linhart Aleš, Tomek Al |
Safe Linkage of Cohort and Population-Based Register Data in a Genomewide Association Study on Health Care Expenditure. Twin research and human genetics : the official journal of the International Society for Twin Studies 2021 7 24 (2): 103-109. de Zeeuw Eveline L, Voort Lykle, Schoonhoven Ruurd, Nivard Michel G, Emery Thomas, Hottenga Jouke-Jan, Willemsen Gonneke A H M, Dykstra Pearl A, Zarrabi Narges, Kartopawiro John D, Boomsma Dorret |
Molecular medicine tumor board: whole-genome sequencing to inform on personalized medicine for a man with advanced prostate cancer. Prostate cancer and prostatic diseases 2021 2 24 (3): 786-793. Armstrong Andrew J, Li Xiaotong, Tucker Matthew, Li Shantao, Mu Xinmeng Jasmine, Eng Kenneth Wha, Sboner Andrea, Rubin Mark, Gerstein Ma |
[Neurogenetics of schizophrenia: findings from studies based on data sharing and global partnerships]. Der Nervenarzt 2021 1 92 (3): 199-207. Adorjan K, Schulze T G, Budde M, Heilbronner U, Tessema F, Mekonnen Z, Falkai |
Is blockchain the breakthrough we are looking for to facilitate genomic data sharing? The European Union perspective. Digital health 2022 7 8 20552076221114225. Cascini Fidelia, Beccia Flavia, Causio Francesco A, Gentili Andrea, Melnyk Andriy, Boccia Stefania, Ricciardi Walt |
Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes. Genetics in medicine : official journal of the American College of Medical Genetics 2022 3 24 (6): 1336-1348. Cohen Ana S A, Farrow Emily G, Abdelmoity Ahmed T, Alaimo Joseph T, Amudhavalli Shivarajan M, Anderson John T, Bansal Lalit, Bartik Lauren, Baybayan Primo, Belden Bradley, Berrios Courtney D, Biswell Rebecca L, Buczkowicz Pawel, Buske Orion, Chakraborty Shreyasee, Cheung Warren A, Coffman Keith A, Cooper Ashley M, Cross Laura A, Curran Tom, Dang Thuy Tien T, Elfrink Mary M, Engleman Kendra L, Fecske Erin D, Fieser Cynthia, Fitzgerald Keely, Fleming Emily A, Gadea Randi N, Gannon Jennifer L, Gelineau-Morel Rose N, Gibson Margaret, Goldstein Jeffrey, Grundberg Elin, Halpin Kelsee, Harvey Brian S, Heese Bryce A, Hein Wendy, Herd Suzanne M, Hughes Susan S, Ilyas Mohammed, Jacobson Jill, Jenkins Janda L, Jiang Shao, Johnston Jeffrey J, Keeler Kathryn, Korlach Jonas, Kussmann Jennifer, Lambert Christine, Lawson Caitlin, Le Pichon Jean-Baptiste, Leeder James Steven, Little Vicki C, Louiselle Daniel A, Lypka Michael, McDonald Brittany D, Miller Neil, Modrcin Ann, Nair Annapoorna, Neal Shelby H, Oermann Christopher M, Pacicca Donna M, Pawar Kailash, Posey Nyshele L, Price Nigel, Puckett Laura M B, Quezada Julio F, Raje Nikita, Rowell William J, Rush Eric T, Sampath Venkatesh, Saunders Carol J, Schwager Caitlin, Schwend Richard M, Shaffer Elizabeth, Smail Craig, Soden Sarah, Strenk Meghan E, Sullivan Bonnie R, Sweeney Brooke R, Tam-Williams Jade B, Walter Adam M, Welsh Holly, Wenger Aaron M, Willig Laurel K, Yan Yun, Younger Scott T, Zhou Dihong, Zion Tricia N, Thiffault Isabelle, Pastinen To |
Auditory oddball hypoactivation in schizophrenia. Psychiatry research. Neuroimaging 2023 9 335 111710. Soichiro Nakahara, Alie G Male, Jessica A Turner, Vince D Calhoun, Kelvin O Lim, Bryon A Mueller, Juan R Bustillo, Daniel S O'Leary, James Voyvodic, Aysenil Belger, Adrian Preda, Daniel H Mathalon, Judith M Ford, Guia Guffanti, Fabio Macciardi, Steven G Potkin, Theo G M Van E |
DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts. BJPsych open 2023 2 9 (2): e32. Lynham Amy J, Knott Sarah, Underwood Jack F G, Hubbard Leon, Agha Sharifah S, Bisson Jonathan I, van den Bree Marianne B M, Chawner Samuel J R A, Craddock Nicholas, O'Donovan Michael, Jones Ian R, Kirov George, Langley Kate, Martin Joanna, Rice Frances, Roberts Neil P, Thapar Anita, Anney Richard, Owen Michael J, Hall Jeremy, Pardiñas Antonio F, Walters James T |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: