Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: BBS9[original query] |
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Capitalizing on admixture in genome-wide association studies: a two-stage testing procedure and application to height in African-Americans. Frontiers in genetics 2011 2 . Kang Guolian, Gao Guimin, Shete Sanjay, Redden David T, Chang Bao-Li, Rebbeck Timothy R, Barnholtz-Sloan Jill S, Pajewski Nicholas M, Allison David |
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.
Nature genetics 2012 Nov . Justice CM, Yagnik G, Kim Y, Peter I, Jabs EW, Erazo M, Ye X, Ainehsazan E, Shi L, Cunningham ML, Kimonis V, Roscioli T, Wall SA, Wilkie AO, Stoler J, Richtsmeier JT, Heuzé Y, Sanchez-Lara PA, Buckley MF, Druschel CM, Mills JL, Caggana M, Romitti PA, Kay DM, Senders C, Taub PJ, Klein OD, Boggan J, Zwienenberg-Lee M, Naydenov C, Kim J, Wilson AF, Boyadjiev SA |
Common FSNP variants of fourteen Bardet-Biedl syndrome genes and adult body mass. Obesity (Silver Spring, Md.) 2013 Aug 21 (8): 1684-9. Birk Ruth Z, Ermakov Sergey, Livshits Grego |
Genome-wide association study of acute kidney injury after coronary bypass graft surgery identifies susceptibility loci.
Kidney international 2015 Jun . Stafford-Smith Mark, Li Yi-Ju, Mathew Joseph P, Li Yen-Wei, Ji Yunqi, Phillips-Bute Barbara G, Milano Carmelo A, Newman Mark F, Kraus William E, Kertai Miklos D, Shah Svati H, Podgoreanu Mihai |
Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.
International journal of obesity (2005) 2016 Apr 40 (4): 662-74. Sung Y J, Pérusse L, Sarzynski M A, Fornage M, Sidney S, Sternfeld B, Rice T, Terry J G, Jacobs D R, Katzmarzyk P, Curran J E, Jeffrey Carr J, Blangero J, Ghosh S, Després J-P, Rankinen T, Rao D C, Bouchard |
Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome. American journal of human genetics 2016 Aug 99 (2): 318-36. Lindstrand Anna, Frangakis Stephan, Carvalho Claudia M B, Richardson Ellen B, McFadden Kelsey A, Willer Jason R, Pehlivan Davut, Liu Pengfei, Pediaditakis Igor L, Sabo Aniko, Lewis Richard Alan, Banin Eyal, Lupski James R, Davis Erica E, Katsanis Nichol |
Genetic variants and acute kidney injury: A review of the literature. Journal of critical care 2017 Nov 44 203-211. Larach Daniel B, Engoren Milo C, Schmidt Ellen M, Heung Micha |
Pharmacogenomics and Placebo Response in a Randomized Clinical Trial in Asthma.
Clinical pharmacology and therapeutics 2019 Dec 106 (6): 1261-1267. Wang Rui-Sheng, Croteau-Chonka Damien C, Silverman Edwin K, Loscalzo J, Weiss Scott T, Hall Kathryn |
Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.
BMC cardiovascular disorders 2019 Jan 19 (1): 26. Westphal Sabine, Stoppe Christian, Gruenewald Matthias, Bein Berthold, Renner Jochen, Cremer Jochen, Coburn Mark, Schaelte Gereon, Boening Andreas, Niemann Bernd, Kletzin Frank, Roesner Jan, Strouhal Ulrich, Reyher Christian, Laufenberg-Feldmann Rita, Ferner Marion, Brandes Ivo F, Bauer Martin, Kortgen Andreas, Stehr Sebastian N, Wittmann Maria, Baumgarten Georg, Struck Rafael, Meyer-Treschan Tanja, Kienbaum Peter, Heringlake Matthias, Schoen Julika, Sander Michael, Treskatsch Sascha, Smul Thorsten, Wolwender Ewa, Schilling Thomas, Degenhardt Frauke, Franke Andre, Mucha Soeren, Tittmann Lukas, Kohlhaas Madeline, Fuernau Georg, Brosteanu Oana, Hasenclever Dirk, Zacharowski Kai, Meybohm Patrick, |
Nonsyndromic craniosynostosis: novel coding variants. Pediatric research 2019 1 85 (4): 463-468. Sewda Anshuman, White Sierra R, Erazo Monica, Hao Ke, García-Fructuoso Gemma, Fernández-Rodriguez Ivette, Heuzé Yann, Richtsmeier Joan T, Romitti Paul A, Reva Boris, Jabs Ethylin Wang, Peter In |
Clinical and exome sequencing findings in seven children with Bardet-Biedl syndrome from Turkey. Annals of human genetics 2020 7 85 (1): 27-36. Gumus Evren, Tuncez Ebru, Oz Ozlem, Saka Guvenc Mer |
Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher Syndromes. Genes 2020 1 10 (12): . Jaffal Lama, Joumaa Wissam H, Assi Alexandre, Helou Charles, Cherfan George, Zibara Kazem, Audo Isabelle, Zeitz Christina, El Shamieh Sa |
Exome Sequencing of 21 Bardet-Biedl Syndrome (BBS) Genes to Identify Obesity Variants in 6,851 American Indians. Obesity (Silver Spring, Md.) 2021 2 29 (4): 748-754. Day Samantha E, Muller Yunhua L, Koroglu Cigdem, Kobes Sayuko, Wiedrich Kim, Mahkee Darin, Kim Hye In, Van Hout Cris, Gosalia Nehal, Ye Bin, , Shuldiner Alan R, Knowler William C, Hanson Robert L, Bogardus Clifton, Baier Leslie |
Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic Craniosynostosis. Genes 2022 5 13 (5): . Justice Cristina M, Musolf Anthony M, Cuellar Araceli, Lattanzi Wanda, Simeonov Emil, Kaneva Radka, Paschall Justin, Cunningham Michael, Wilkie Andrew O M, Wilson Alexander F, Romitti Paul A, Boyadjiev Simeon |
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure. Kidney international reports 2023 10 8 (10): 2126-2135. Yishay Ben-Moshe, Omer Shlomovitz, Danit Atias-Varon, Orly Haskin, Efrat Ben-Shalom, Hadas Shasha Lavsky, Oded Volovelsky, Shrikant Mane, Dror Ben-Ruby, Guy Chowers, Karl Skorecki, Yael Borovitz, Maayan Kagan, Nofar Mor, Yulia Khavkin, Shimrit Tzvi-Behr, Shirley Pollack, Moran Plonsky Toder, Michael Geylis, Aviad Schnapp, Rachel Becker-Cohen, Irith Weissman, Ruth Schreiber, Miriam Davidovits, Yaacov Frishberg, Daniella Magen, Ortal Barel, Asaf Vivan |
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- Page last updated:Apr 29, 2024
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