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

Year Number of Results
1991 1
1992 7
1993 7
1994 5
1995 3
1996 1
1997 1
1998 3
1999 2
2000 5
2001 3
2002 6
2003 5
2004 3
2005 3
2006 10
2007 5
2008 7
2009 8
2010 6
2011 8
2012 7
2013 7
2014 18
2015 13
2016 14
2017 7
2018 7
2019 15
2020 8
2021 12
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Search Results

182 results
Results by year
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Page 1
Sexual Orientation, Controversy, and Science.
Bailey JM, Vasey PL, Diamond LM, Breedlove SM, Vilain E, Epprecht M. Bailey JM, et al. Among authors: vilain e. Psychol Sci Public Interest. 2016 Sep;17(2):45-101. doi: 10.1177/1529100616637616. Psychol Sci Public Interest. 2016. PMID: 27113562 Review.
Global Disorders of Sex Development Update since 2006: Perceptions, Approach and Care.
Lee PA, Nordenström A, Houk CP, Ahmed SF, Auchus R, Baratz A, Baratz Dalke K, Liao LM, Lin-Su K, Looijenga LH 3rd, Mazur T, Meyer-Bahlburg HF, Mouriquand P, Quigley CA, Sandberg DE, Vilain E, Witchel S; Global DSD Update Consortium. Lee PA, et al. Among authors: vilain e. Horm Res Paediatr. 2016;85(3):158-80. doi: 10.1159/000442975. Epub 2016 Jan 28. Horm Res Paediatr. 2016. PMID: 26820577 Free article. Review.
Clinical exome sequencing for genetic identification of rare Mendelian disorders.
Lee H, Deignan JL, Dorrani N, Strom SP, Kantarci S, Quintero-Rivera F, Das K, Toy T, Harry B, Yourshaw M, Fox M, Fogel BL, Martinez-Agosto JA, Wong DA, Chang VY, Shieh PB, Palmer CG, Dipple KM, Grody WW, Vilain E, Nelson SF. Lee H, et al. Among authors: vilain e. JAMA. 2014 Nov 12;312(18):1880-7. doi: 10.1001/jama.2014.14604. JAMA. 2014. PMID: 25326637 Free PMC article.
Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients.
Bryant L, Li D, Cox SG, Marchione D, Joiner EF, Wilson K, Janssen K, Lee P, March ME, Nair D, Sherr E, Fregeau B, Wierenga KJ, Wadley A, Mancini GMS, Powell-Hamilton N, van de Kamp J, Grebe T, Dean J, Ross A, Crawford HP, Powis Z, Cho MT, Willing MC, Manwaring L, Schot R, Nava C, Afenjar A, Lessel D, Wagner M, Klopstock T, Winkelmann J, Catarino CB, Retterer K, Schuette JL, Innis JW, Pizzino A, Lüttgen S, Denecke J, Strom TM, Monaghan KG; DDD Study, Yuan ZF, Dubbs H, Bend R, Lee JA, Lyons MJ, Hoefele J, Günthner R, Reutter H, Keren B, Radtke K, Sherbini O, Mrokse C, Helbig KL, Odent S, Cogne B, Mercier S, Bezieau S, Besnard T, Kury S, Redon R, Reinson K, Wojcik MH, Õunap K, Ilves P, Innes AM, Kernohan KD; Care4Rare Canada Consortium, Costain G, Meyn MS, Chitayat D, Zackai E, Lehman A, Kitson H; CAUSES Study, Martin MG, Martinez-Agosto JA; Undiagnosed Diseases Network, Nelson SF, Palmer CGS, Papp JC, Parker NH, Sinsheimer JS, Vilain E, Wan J, Yoon AJ, Zheng A, Brimble E, Ferrero GB, Radio FC, Carli D, Barresi S, Brusco A, Tartaglia M, Thomas JM, Umana L, Weiss MM, Gotway G, Stuurman KE, Thompson ML, McWalter K, Stumpel CTRM, Stevens SJC, Stegmann APA, Tveten K, Vøllo A, Prescott T, Fagerberg C, Laulund LW, Larsen MJ, Byler M, Lebel RR, Hurst AC, Dean J, Schrier Vergano SA, Norman J, Mercimek-Andrews S, Neira J, Van Allen MI, Longo N, Sellars E, Louie RJ, Cathey SS, Brokamp E, Heron D, Snyder M, Vanderver A, Simon C, de la Cruz X, Padilla N, Crump JG, Chung W, Garcia B, Hakonarson HH, Bhoj EJ. Bryant L, et al. Among authors: vilain e. Sci Adv. 2020 Dec 2;6(49):eabc9207. doi: 10.1126/sciadv.abc9207. Print 2020 Dec. Sci Adv. 2020. PMID: 33268356 Free PMC article.
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals.
Ng BG, Sosicka P, Agadi S, Almannai M, Bacino CA, Barone R, Botto LD, Burton JE, Carlston C, Chung BH, Cohen JS, Coman D, Dipple KM, Dorrani N, Dobyns WB, Elias AF, Epstein L, Gahl WA, Garozzo D, Hammer TB, Haven J, Héron D, Herzog M, Hoganson GE, Hunter JM, Jain M, Juusola J, Lakhani S, Lee H, Lee J, Lewis K, Longo N, Lourenço CM, Mak CCY, McKnight D, Mendelsohn BA, Mignot C, Mirzaa G, Mitchell W, Muhle H, Nelson SF, Olczak M, Palmer CGS, Partikian A, Patterson MC, Pierson TM, Quinonez SC, Regan BM, Ross ME, Guillen Sacoto MJ, Scaglia F, Scheffer IE, Segal D, Singhal NS, Striano P, Sturiale L, Symonds JD, Tang S, Vilain E, Willis M, Wolfe LA, Yang H, Yano S, Powis Z, Suchy SF, Rosenfeld JA, Edmondson AC, Grunewald S, Freeze HH. Ng BG, et al. Among authors: vilain e. Hum Mutat. 2019 Jul;40(7):908-925. doi: 10.1002/humu.23731. Epub 2019 Apr 24. Hum Mutat. 2019. PMID: 30817854 Free PMC article.
COVID-19 and the International Academy of Sex Research: We Will Be Back.
Mustanski B, Vilain E, Dworkin SL, Suschinsky KD, Zucker KJ. Mustanski B, et al. Among authors: vilain e. Arch Sex Behav. 2020 Jul;49(5):1401. doi: 10.1007/s10508-020-01735-6. Arch Sex Behav. 2020. PMID: 32399914 Free PMC article. No abstract available.
Genetics of Disorders of Sex Development: The DSD-TRN Experience.
Délot EC, Papp JC; DSD-TRN Genetics Workgroup, Sandberg DE, Vilain E. Délot EC, et al. Among authors: vilain e. Endocrinol Metab Clin North Am. 2017 Jun;46(2):519-537. doi: 10.1016/j.ecl.2017.01.015. Epub 2017 Mar 28. Endocrinol Metab Clin North Am. 2017. PMID: 28476235 Free PMC article. Review.
[Sex genetics].
Vilain E, Elreavey KM, Richaud F, Fellous M. Vilain E, et al. Presse Med. 1992 May 16;21(18):852-6. Presse Med. 1992. PMID: 1535151 Review. French.
The importance of having two X chromosomes.
Arnold AP, Reue K, Eghbali M, Vilain E, Chen X, Ghahramani N, Itoh Y, Li J, Link JC, Ngun T, Williams-Burris SM. Arnold AP, et al. Among authors: vilain e. Philos Trans R Soc Lond B Biol Sci. 2016 Feb 19;371(1688):20150113. doi: 10.1098/rstb.2015.0113. Epub 2016 Feb 1. Philos Trans R Soc Lond B Biol Sci. 2016. PMID: 26833834 Free PMC article. Review.
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