BRCA Share: A Collection of Clinical BRCA Gene Variants

https://phgkb.cdc.gov/GAPPKB/phgHome.do

From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• BRCA Share: A Collection of Clinical BRCA Gene Variants.  
  Human mutation 2016 Sep .
  Beroud Christophe, Letovsky Stanley I, Braastad Corey D, Caputo Sandrine M, Beaudoux Olivia, Bignon Yves Jean, De Paillerets Brigitte Bressac-, Bronner Myriam, Buell Crystal M, Collod-Béroud Gwenaëlle, Coulet Florence, Derive Nicolas, Divincenzo Christina, Elzinga Christopher D, Garrec Céline, Houdayer Claude, Karbassi Izabela, Lizard Sarab, Love Angela, Muller Danièle, Nagan Narasimhan, Nery Camille R, Rai Ghadi, Revillion Françoise, Salgado David, Sévenet Nicolas, Sinilnikova Olga, Sobol Hagay, Stoppa-Lyonnet Dominique, Toulas Christine, Trautman Edwin, Vaur Dominique, Vilquin Paul, Weymouth Katelyn S, Willis Alecia, , , , Eisenberg Marcia, Strom Charles
• 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
• 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

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