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

Year Number of Results
2002 1
2007 2
2008 3
2009 4
2010 2
2012 1
2013 1
2014 3
2015 2
2016 3
2017 1
2018 1
2019 1
2020 1
2021 2
2022 4
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26 results
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Page 1
Genetics, Meiosis.
Gottlieb SF, Gulani A, Tegay DH. Gottlieb SF, et al. Among authors: tegay dh. 2021 Aug 11. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan–. 2021 Aug 11. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan–. PMID: 29494069 Free Books & Documents.
Genetics, Nondisjunction.
Gottlieb SF, Tupper C, Kerndt CC, Tegay DH. Gottlieb SF, et al. Among authors: tegay dh. 2021 Aug 11. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan–. 2021 Aug 11. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan–. PMID: 29489267 Free Books & Documents.
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
Kuechler A, Willemsen MH, Albrecht B, Bacino CA, Bartholomew DW, van Bokhoven H, van den Boogaard MJ, Bramswig N, Büttner C, Cremer K, Czeschik JC, Engels H, van Gassen K, Graf E, van Haelst M, He W, Hogue JS, Kempers M, Koolen D, Monroe G, de Munnik S, Pastore M, Reis A, Reuter MS, Tegay DH, Veltman J, Visser G, van Hasselt P, Smeets EE, Vissers L, Wieland T, Wissink W, Yntema H, Zink AM, Strom TM, Lüdecke HJ, Kleefstra T, Wieczorek D. Kuechler A, et al. Among authors: tegay dh. Hum Genet. 2015 Jan;134(1):97-109. doi: 10.1007/s00439-014-1498-1. Epub 2014 Oct 19. Hum Genet. 2015. PMID: 25326669
6-Mercaptopurine teratogenicity.
Tegay DH, Tepper R, Willner JP. Tegay DH, et al. Postgrad Med J. 2002 Sep;78(923):572; author reply 572. doi: 10.1136/pmj.78.923.572-a. Postgrad Med J. 2002. PMID: 12357029 Free PMC article. No abstract available.
Acceptance of technology-based tools in a sample of Parkinson's patients.
Duroseau N, Abramson T, Pergament K, Chan V, Govindavari JP, Ciraco C, Tegay D, Krishnamachari B. Duroseau N, et al. Among authors: tegay d. Chronic Illn. 2017 Mar;13(1):3-13. doi: 10.1177/1742395316653453. Epub 2016 Jul 8. Chronic Illn. 2017. PMID: 27269275
KBG syndrome involving a single-nucleotide duplication in ANKRD11.
Kleyner R, Malcolmson J, Tegay D, Ward K, Maughan A, Maughan G, Nelson L, Wang K, Robison R, Lyon GJ. Kleyner R, et al. Among authors: tegay d. Cold Spring Harb Mol Case Stud. 2016 Nov;2(6):a001131. doi: 10.1101/mcs.a001131. Cold Spring Harb Mol Case Stud. 2016. PMID: 27900361 Free PMC article.
Physician Risk Assessment Knowledge Regarding BRCA Genetics Testing.
Cohn J, Blazey W, Tegay D, Harper B, Koehler S, Laurent B, Chan V, Jung MK, Krishnamachari B. Cohn J, et al. Among authors: tegay d. J Cancer Educ. 2015 Sep;30(3):573-9. doi: 10.1007/s13187-014-0724-9. J Cancer Educ. 2015. PMID: 25234477
Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide.
Gonzaga-Jauregui C, Yesil G, Nistala H, Gezdirici A, Bayram Y, Nannuru KC, Pehlivan D, Yuan B, Jimenez J, Sahin Y, Paine IS, Akdemir ZC, Rajamani S, Staples J, Dronzek J, Howell K, Fatih JM, Smaldone S, Schlesinger AE, Ramírez N, Cornier AS, Kelly MA, Haber R, Chim SM, Nieman K, Wu N, Walls J; Baylor-Hopkins Center for Mendelian Genetics, Regeneron Genetics Center, Poueymirou W, Siao CJ, Sutton VR, Williams MS, Posey JE, Gibbs RA, Carlo S, Tegay DH, Economides AN, Lupski JR. Gonzaga-Jauregui C, et al. Among authors: tegay dh. Eur J Hum Genet. 2020 Sep;28(9):1243-1264. doi: 10.1038/s41431-020-0632-x. Epub 2020 May 6. Eur J Hum Genet. 2020. PMID: 32376988 Free PMC article.
26 results