[Exploring parent-of-origin effects for non-syndromic cleft lip with or without cleft palate on PTCH1, PTCH2, SHH, SMO genes in Chinese case-parent trios].
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal Of Peking University. Health Sciences
Li, W Y WY; Wang, M Y MY; Zhou, R R; Wang, S Y SY; Zheng, H C HC; Zhu, H P HP; Zhou, Z B ZB; Wu, T T; Wang, H H; Shi, B B
Association between PTCH1 gene polymorphisms and chronic obstructive pulmonary disease susceptibility in a Chinese Han population: a case-control study.
Chinese Medical Journal
Kang, Xi X; Guo, Ting T; Liu, Lyu L; Ding, Shui-Zi SZ; Lei, Cheng C; Luo, Hong H
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene.
Genes
van Rooij, Iris Alm IA; Ludwig, Kerstin U KU; Welzenbach, Julia J; Ishorst, Nina N; Thonissen, Michelle M; Galesloot, Tessel E TE; Ongkosuwito, Edwin E; Bergé, Stefaan J SJ; Aldhorae, Khalid K; Rojas-Martinez, Augusto A; Kiemeney, Lambertus Alm LA; Vermeesch, Joris Robert JR; Brunner, Han H; Roeleveld, Nel N; Devriendt, Koen K; Dormaar, Titiaan T; Hens, Greet G; Knapp, Michael M; Carels, Carine C; Mangold, Elisabeth E
Genomic analyses in African populations identify novel risk loci for cleft palate.
Human Molecular Genetics
Butali, Azeez A; Mossey, Peter A PA; Adeyemo, Wasiu L WL; Eshete, Mekonen A MA; Gowans, Lord J J LJJ; Busch, Tamara D TD; Jain, Deepti D; Yu, Wenjie W; Huan, Liu L; Laurie, Cecelia A CA; Laurie, Cathy C CC; Nelson, Sarah S; Li, Mary M; Sanchez-Lara, Pedro A PA; Magee, William P WP; Magee, Kathleen S KS; Auslander, Allyn A; Brindopke, Frederick F; Kay, Denise M DM; Caggana, Michele M; Romitti, Paul A PA; Mills, James L JL; Audu, Rosemary R; Onwuamah, Chika C; Oseni, Ganiyu O GO; Owais, Arwa A; James, Olutayo O; Olaitan, Peter B PB; Aregbesola, Babatunde S BS; Braimah, Ramat O RO; Oginni, Fadekemi O FO; Oladele, Ayodeji O AO; Bello, Saidu A SA; Rhodes, Jennifer J; Shiang, Rita R; Donkor, Peter P; Obiri-Yeboah, Solomon S; Arthur, Fareed Kow Nanse FKN; Twumasi, Peter P; Agbenorku, Pius P; Plange-Rhule, Gyikua G; Oti, Alexander Acheampong AA; Ogunlewe, Olugbenga M OM; Oladega, Afisu A AA; Adekunle, Adegbayi A AA; Erinoso, Akinwunmi O AO; Adamson, Olatunbosun O OO; Elufowoju, Abosede A AA; Ayelomi, Oluwanifemi I OI; Hailu, Taiye T; Hailu, Abiye A; Demissie, Yohannes Y; Derebew, Miliard M; Eliason, Steve S; Romero-Bustillous, Miguel M; Lo, Cynthia C; Park, James J; Desai, Shaan S; Mohammed, Muiawa M; Abate, Firke F; Abdur-Rahman, Lukman O LO; Anand, Deepti D; Saadi, Irfaan I; Oladugba, Abimibola V AV; Lachke, Salil A SA; Amendt, Brad A BA; Rotimi, Charles N CN; Marazita, Mary L ML; Cornell, Robert A RA; Murray, Jeffrey C JC; Adeyemo, Adebowale A AA
Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation.
Frontiers In Genetics
Indencleef, Karlijne K; Roosenboom, Jasmien J; Hoskens, Hanne H; White, Julie D JD; Shriver, Mark D MD; Richmond, Stephen S; Peeters, Hilde H; Feingold, Eleanor E; Marazita, Mary L ML; Shaffer, John R JR; Weinberg, Seth M SM; Hens, Greet G; Claes, Peter P
Structural variants caused by Alu insertions are associated with risks for many human diseases.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Payer, Lindsay M LM; Steranka, Jared P JP; Yang, Wan Rou WR; Kryatova, Maria M; Medabalimi, Sibyl S; Ardeljan, Daniel D; Liu, Chunhong C; Boeke, Jef D JD; Avramopoulos, Dimitri D; Burns, Kathleen H KH
A systematic SNP selection approach to identify mechanisms underlying disease aetiology: linking height to post-menopausal breast and colorectal cancer risk.
Scientific Reports
Elands, Rachel J J RJ; Simons, Colinda C J M CC; Riemenschneider, Mona M; Isaacs, Aaron A; Schouten, Leo J LJ; Verhage, Bas A BA; Van Steen, Kristel K; Godschalk, Roger W L RW; van den Brandt, Piet A PA; Stoll, Monika M; Weijenberg, Matty P MP
Molecular mechanisms underlying variations in lung function: a systems genetics analysis.
The Lancet. Respiratory Medicine
Obeidat, Ma'en M; Hao, Ke K; Bossé, Yohan Y; Nickle, David C DC; Nie, Yunlong Y; Postma, Dirkje S DS; Laviolette, Michel M; Sandford, Andrew J AJ; Daley, Denise D DD; Hogg, James C JC; Elliott, W Mark WM; Fishbane, Nick N; Timens, Wim W; Hysi, Pirro G PG; Kaprio, Jaakko J; Wilson, James F JF; Hui, Jennie J; Rawal, Rajesh R; Schulz, Holger H; Stubbe, Beate B; Hayward, Caroline C; Polasek, Ozren O; Järvelin, Marjo-Riitta MR; Zhao, Jing Hua JH; Jarvis, Deborah D; Kähönen, Mika M; Franceschini, Nora N; North, Kari E KE; Loth, Daan W DW; Brusselle, Guy G GG; Smith, Albert Vernon AV; Gudnason, Vilmundur V; Bartz, Traci M TM; Wilk, Jemma B JB; O'Connor, George T GT; Cassano, Patricia A PA; Tang, Wenbo W; Wain, Louise V LV; Soler Artigas, María M; Gharib, Sina A SA; Strachan, David P DP; Sin, Don D DD; Tobin, Martin D MD; London, Stephanie J SJ; Hall, Ian P IP; Paré, Peter D PD
CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma.
Journal Of Neuro-Oncology
Dahlin, Anna M AM; Hollegaard, Mads V MV; Wibom, Carl C; Andersson, Ulrika U; Hougaard, David M DM; Deltour, Isabelle I; Hjalmars, Ulf U; Melin, Beatrice B
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits.
Nature Genetics
Yang, Jian J; Ferreira, Teresa T; Morris, Andrew P AP; Medland, Sarah E SE; , ; , ; Madden, Pamela A F PA; Heath, Andrew C AC; Martin, Nicholas G NG; Montgomery, Grant W GW; Weedon, Michael N MN; Loos, Ruth J RJ; Frayling, Timothy M TM; McCarthy, Mark I MI; Hirschhorn, Joel N JN; Goddard, Michael E ME; Visscher, Peter M PM
Genetic contributions to the association between adult height and testicular germ cell tumors.
International Journal Of Epidemiology
Cook, Michael B MB; Chia, Victoria M VM; Berndt, Sonja I SI; Graubard, Barry I BI; Chanock, Stephen J SJ; Rubertone, Mark V MV; Erickson, Ralph L RL; Hayes, Richard B RB; McGlynn, Katherine A KA
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.
American Journal Of Human Genetics
Lanktree, Matthew B MB; Guo, Yiran Y; Murtaza, Muhammed M; Glessner, Joseph T JT; Bailey, Swneke D SD; Onland-Moret, N Charlotte NC; Lettre, Guillaume G; Ongen, Halit H; Rajagopalan, Ramakrishnan R; Johnson, Toby T; Shen, Haiqing H; Nelson, Christopher P CP; Klopp, Norman N; Baumert, Jens J; Padmanabhan, Sandosh S; Pankratz, Nathan N; Pankow, James S JS; Shah, Sonia S; Taylor, Kira K; Barnard, John J; Peters, Bas J BJ; Maloney, Cliona M CM; Lobmeyer, Maximilian T MT; Stanton, Alice A; Zafarmand, M Hadi MH; Romaine, Simon P R SP; Mehta, Amar A; van Iperen, Erik P A EP; Gong, Yan Y; Price, Tom S TS; Smith, Erin N EN; Kim, Cecilia E CE; Li, Yun R YR; Asselbergs, Folkert W FW; Atwood, Larry D LD; Bailey, Kristian M KM; Bhatt, Deepak D; Bauer, Florianne F; Behr, Elijah R ER; Bhangale, Tushar T; Boer, Jolanda M A JM; Boehm, Bernhard O BO; Bradfield, Jonathan P JP; Brown, Morris M; Braund, Peter S PS; Burton, Paul R PR; Carty, Cara C; Chandrupatla, Hareesh R HR; Chen, Wei W; Connell, John J; Dalgeorgou, Chrysoula C; Boer, Anthonius de Ad; Drenos, Fotios F; Elbers, Clara C CC; Fang, James C JC; Fox, Caroline S CS; Frackelton, Edward C EC; Fuchs, Barry B; Furlong, Clement E CE; Gibson, Quince Q; Gieger, Christian C; Goel, Anuj A; Grobbee, Diederik E DE; Hastie, Claire C; Howard, Philip J PJ; Huang, Guan-Hua GH; Johnson, W Craig WC; Li, Qing Q; Kleber, Marcus E ME; Klein, Barbara E K BE; Klein, Ronald R; Kooperberg, Charles C; Ky, Bonnie B; Lacroix, Andrea A; Lanken, Paul P; Lathrop, Mark M; Li, Mingyao M; Marshall, Vanessa V; Melander, Olle O; Mentch, Frank D FD; Meyer, Nuala J NJ; Monda, Keri L KL; Montpetit, Alexandre A; Murugesan, Gurunathan G; Nakayama, Karen K; Nondahl, Dave D; Onipinla, Abiodun A; Rafelt, Suzanne S; Newhouse, Stephen J SJ; Otieno, F George FG; Patel, Sanjey R SR; Putt, Mary E ME; Rodriguez, Santiago S; Safa, Radwan N RN; Sawyer, Douglas B DB; Schreiner, Pamela J PJ; Simpson, Claire C; Sivapalaratnam, Suthesh S; Srinivasan, Sathanur R SR; Suver, Christine C; Swergold, Gary G; Sweitzer, Nancy K NK; Thomas, Kelly A KA; Thorand, Barbara B; Timpson, Nicholas J NJ; Tischfield, Sam S; Tobin, Martin M; Tomaszewski, Maciej M; Tomaszweski, Maciej M; Verschuren, W M Monique WM; Wallace, Chris C; Winkelmann, Bernhard B; Zhang, Haitao H; Zheng, Dongling D; Zhang, Li L; Zmuda, Joseph M JM; Clarke, Robert R; Balmforth, Anthony J AJ; Danesh, John J; Day, Ian N IN; Schork, Nicholas J NJ; de Bakker, Paul I W PI; Delles, Christian C; Duggan, David D; Hingorani, Aroon D AD; Hirschhorn, Joel N JN; Hofker, Marten H MH; Humphries, Steve E SE; Kivimaki, Mika M; Lawlor, Debbie A DA; Kottke-Marchant, Kandice K; Mega, Jessica L JL; Mitchell, Braxton D BD; Morrow, David A DA; Palmen, Jutta J; Redline, Susan S; Shields, Denis C DC; Shuldiner, Alan R AR; Sleiman, Patrick M PM; Smith, George Davey GD; Farrall, Martin M; Jamshidi, Yalda Y; Christiani, David C DC; Casas, Juan P JP; Hall, Alistair S AS; Doevendans, Pieter A PA; Christie, Jason D JD; Berenson, Gerald S GS; Murray, Sarah S SS; Illig, Thomas T; Dorn, Gerald W GW; Cappola, Thomas P TP; Boerwinkle, Eric E; Sever, Peter P; Rader, Daniel J DJ; Reilly, Muredach P MP; Caulfield, Mark M; Talmud, Philippa J PJ; Topol, Eric E; Engert, James C JC; Wang, Kai K; Dominiczak, Anna A; Hamsten, Anders A; Curtis, Sean P SP; Silverstein, Roy L RL; Lange, Leslie A LA; Sabatine, Marc S MS; Trip, Mieke M; Saleheen, Danish D; Peden, John F JF; Cruickshanks, Karen J KJ; März, Winfried W; O'Connell, Jeffrey R JR; Klungel, Olaf H OH; Wijmenga, Cisca C; Maitland-van der Zee, Anke Hilse AH; Schadt, Eric E EE; Johnson, Julie A JA; Jarvik, Gail P GP; Papanicolaou, George J GJ; , ; Grant, Struan F A SF; Munroe, Patricia B PB; North, Kari E KE; Samani, Nilesh J NJ; Koenig, Wolfgang W; Gaunt, Tom R TR; Anand, Sonia S SS; van der Schouw, Yvonne T YT; , ; Soranzo, Nicole N; Fitzgerald, Garret A GA; Reiner, Alex A; Hegele, Robert A RA; Hakonarson, Hakon H; Keating, Brendan J BJ
Follow-up association studies of chromosome region 9q and nonsyndromic cleft lip/palate.
American Journal Of Medical Genetics. Part A
Letra, Ariadne A; Menezes, Renato R; Govil, Manika M; Fonseca, Renata F RF; McHenry, Toby T; Granjeiro, José M JM; Castilla, Eduardo E EE; Orioli, Iêda M IM; Marazita, Mary L ML; Vieira, Alexandre R AR
Genome-wide association study of height and body mass index in Australian twin families.
Twin Research And Human Genetics : The Official Journal Of The International Society For Twin Studies
Liu, Jimmy Z JZ; Medland, Sarah E SE; Wright, Margaret J MJ; Henders, Anjali K AK; Heath, Andrew C AC; Madden, Pamela A F PA; Duncan, Alexis A; Montgomery, Grant W GW; Martin, Nicholas G NG; McRae, Allan F AF
Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs.
Human Molecular Genetics
Tönjes, Anke A; Koriath, Moritz M; Schleinitz, Dorit D; Dietrich, Kerstin K; Böttcher, Yvonne Y; Rayner, Nigel W NW; Almgren, Peter P; Enigk, Beate B; Richter, Olaf O; Rohm, Silvio S; Fischer-Rosinsky, Antje A; Pfeiffer, Andreas A; Hoffmann, Katrin K; Krohn, Knut K; Aust, Gabriela G; Spranger, Joachim J; Groop, Leif L; Blüher, Matthias M; Kovacs, Peter P; Stumvoll, Michael M
Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966.
Plos Genetics
Sovio, Ulla U; Bennett, Amanda J AJ; Millwood, Iona Y IY; Molitor, John J; O'Reilly, Paul F PF; Timpson, Nicholas J NJ; Kaakinen, Marika M; Laitinen, Jaana J; Haukka, Jari J; Pillas, Demetris D; Tzoulaki, Ioanna I; Molitor, Jassy J; Hoggart, Clive C; Coin, Lachlan J M LJ; Whittaker, John J; Pouta, Anneli A; Hartikainen, Anna-Liisa AL; Freimer, Nelson B NB; Widen, Elisabeth E; Peltonen, Leena L; Elliott, Paul P; McCarthy, Mark I MI; Jarvelin, Marjo-Riitta MR
Genome-wide association analysis identifies 20 loci that influence adult height.
Nature Genetics
Weedon, Michael N MN; Lango, Hana H; Lindgren, Cecilia M CM; Wallace, Chris C; Evans, David M DM; Mangino, Massimo M; Freathy, Rachel M RM; Perry, John R B JR; Stevens, Suzanne S; Hall, Alistair S AS; Samani, Nilesh J NJ; Shields, Beverly B; Prokopenko, Inga I; Farrall, Martin M; Dominiczak, Anna A; , ; , ; Johnson, Toby T; Bergmann, Sven S; Beckmann, Jacques S JS; Vollenweider, Peter P; Waterworth, Dawn M DM; Mooser, Vincent V; Palmer, Colin N A CN; Morris, Andrew D AD; Ouwehand, Willem H WH; , ; Zhao, Jing Hua JH; Li, Shengxu S; Loos, Ruth J F RJ; Barroso, Inês I; Deloukas, Panagiotis P; Sandhu, Manjinder S MS; Wheeler, Eleanor E; Soranzo, Nicole N; Inouye, Michael M; Wareham, Nicholas J NJ; Caulfield, Mark M; Munroe, Patricia B PB; Hattersley, Andrew T AT; McCarthy, Mark I MI; Frayling, Timothy M TM