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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1986 1
1987 3
1988 2
1989 1
1990 5
1991 1
1992 2
1993 2
1994 6
1995 3
1997 1
1998 2
1999 3
2000 3
2001 1
2002 3
2003 2
2004 3
2005 3
2006 4
2007 3
2008 4
2009 2
2010 2
2011 7
2012 5
2013 7
2014 6
2015 6
2016 1
2017 1
2018 1
2020 1
2021 3
2022 3
2023 3
2024 1

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99 results

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Page 1
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes.
Wheway G, Schmidts M, Mans DA, Szymanska K, Nguyen TT, Racher H, Phelps IG, Toedt G, Kennedy J, Wunderlich KA, Sorusch N, Abdelhamed ZA, Natarajan S, Herridge W, van Reeuwijk J, Horn N, Boldt K, Parry DA, Letteboer SJF, Roosing S, Adams M, Bell SM, Bond J, Higgins J, Morrison EE, Tomlinson DC, Slaats GG, van Dam TJP, Huang L, Kessler K, Giessl A, Logan CV, Boyle EA, Shendure J, Anazi S, Aldahmesh M, Al Hazzaa S, Hegele RA, Ober C, Frosk P, Mhanni AA, Chodirker BN, Chudley AE, Lamont R, Bernier FP, Beaulieu CL, Gordon P, Pon RT, Donahue C, Barkovich AJ, Wolf L, Toomes C, Thiel CT, Boycott KM, McKibbin M, Inglehearn CF; UK10K Consortium; University of Washington Center for Mendelian Genomics; Stewart F, Omran H, Huynen MA, Sergouniotis PI, Alkuraya FS, Parboosingh JS, Innes AM, Willoughby CE, Giles RH, Webster AR, Ueffing M, Blacque O, Gleeson JG, Wolfrum U, Beales PL, Gibson T, Doherty D, Mitchison HM, Roepman R, Johnson CA. Wheway G, et al. Among authors: chodirker bn. Nat Cell Biol. 2015 Aug;17(8):1074-1087. doi: 10.1038/ncb3201. Epub 2015 Jul 13. Nat Cell Biol. 2015. PMID: 26167768 Free PMC article.
Recurrent miscarriage.
Chodirker BN, Dawson AJ. Chodirker BN, et al. N Engl J Med. 2011 Feb 24;364(8):783; author reply 784. doi: 10.1056/NEJMc1014103. N Engl J Med. 2011. PMID: 21345124 No abstract available.
Severe acro-renal-uterine-mandibular syndrome.
Evans JA, Phillips S, Reed M, Chodirker BN. Evans JA, et al. Among authors: chodirker bn. Am J Med Genet. 2000 Jul 3;93(1):67-73. doi: 10.1002/1096-8628(20000703)93:1<67::aid-ajmg11>3.0.co;2-k. Am J Med Genet. 2000. PMID: 10861684
Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability.
Lee YR, Thomas MG, Roychaudhury A, Skinner C, Maconachie G, Crosier M, Horak H, Constantinescu CS, Choi TI, Kyung JJ, Wang T, Ku B, Chodirker BN, Hammer MF, Gottlob I, Norton WHJ, Chudley AE, Schwartz CE, Kim CH. Lee YR, et al. Among authors: chodirker bn. Res Sq [Preprint]. 2023 Mar 20:rs.3.rs-2683050. doi: 10.21203/rs.3.rs-2683050/v1. Res Sq. 2023. PMID: 36993381 Free PMC article. Preprint.
A Canadian Provincial Screening Program for Lynch Syndrome.
Stone JK, Winter R, Khan D, Rothenmund H, Klein J, Chodirker B, Wightman R, Kim CA, Nugent Z, Singh H. Stone JK, et al. Among authors: chodirker b. Am J Gastroenterol. 2023 Feb 1;118(2):345-353. doi: 10.14309/ajg.0000000000002059. Epub 2022 Oct 11. Am J Gastroenterol. 2023. PMID: 36219179
Clinical genetics and the Hutterite population: a review of Mendelian disorders.
Boycott KM, Parboosingh JS, Chodirker BN, Lowry RB, McLeod DR, Morris J, Greenberg CR, Chudley AE, Bernier FP, Midgley J, Møller LB, Innes AM. Boycott KM, et al. Among authors: chodirker bn. Am J Med Genet A. 2008 Apr 15;146A(8):1088-98. doi: 10.1002/ajmg.a.32245. Am J Med Genet A. 2008. PMID: 18348266 Review.
Province-Wide Ascertainment of Lynch Syndrome in Manitoba.
Rothenmund H, Lambert P, Khan D, Kim C, Sharma B, Serfas K, Chodirker B, Singh H. Rothenmund H, et al. Among authors: chodirker b. Clin Gastroenterol Hepatol. 2024 Mar;22(3):642-652.e2. doi: 10.1016/j.cgh.2023.10.005. Epub 2023 Oct 23. Clin Gastroenterol Hepatol. 2024. PMID: 37879520
Routine genetic testing for Asperger syndrome.
Chodirker BN, Chudley AE. Chodirker BN, et al. Genet Med. 2008 Nov;10(11):843-5; author reply 845. doi: 10.1097/GIM.0b013e31818b0c76. Genet Med. 2008. PMID: 18941416 Free article. No abstract available.
99 results