" Sexual orientation, controversy, and science": Erratum. JM Bailey, PL Vasey, LM Diamond, SM Breedlove, E Vilain, M Epprecht Sage Publications, 2017 | 2 | 2017 |
“Straight-acting gays”: The relationship between masculine consciousness, anti-effeminacy, and negative gay identity FJ Sánchez, E Vilain Archives of sexual behavior 41, 111-119, 2012 | 277 | 2012 |
11Chapter EJN Vilain HANDBOOK OF, 329, 2008 | | 2008 |
1280: Increased Susceptibility to Genitovaginal Prolapse Associated with a Polymorphism in the Promoter of the Extracellular Matrix Protein LAMC1 G Nikolova, CO Twiss, H Lee, N Stanley, J Sinsheimer, E Vilain, ... The Journal of Urology 177 (4S), 421-422, 2007 | | 2007 |
3. Optical genome mapping reveals novel structural variants in pediatric high grade gliomas M Bornhorst, S Bhattacharya, Y Fu, A Eze, D Morinigo, J Nazarian, ... Cancer Genetics 260, 2, 2022 | | 2022 |
46, XX TRUE HERMAPHRODITES POSITIVE FOR Y-DNA SEQUENCE N ABBAS, R BRAUNER, E VILAIN, F RICHAUD, C MOREIRA, ... CYTOGENETICS AND CELL GENETICS 58 (3-4), 2093-2093, 1991 | | 1991 |
46, XX true hermaphroditism associated with a terminal deletion of the short arm of the X chromosome S Barbaux, E Vilain, K McElreavey American Journal of Human Genetics 55 (CONF-941009-), 1994 | | 1994 |
57. Identification of key molecular mechanisms in IDH-mutant brain tumors to enable precise risk stratification S Bhattacharya, A Dawood, H Barseghyan, E Vilain, M Bornhorst Cancer Genetics 268, 18-19, 2022 | | 2022 |
859: Autosomal Dominant Tranmission of Genitovaginal Prolapse GS Jack, R Bukkapatnam, G Nicolav, E Vilain, LV Rodriguez The Journal of Urology 173 (4S), 233-234, 2005 | 1 | 2005 |
A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative V Shashi, K Schoch, R Spillmann, H Cope, QKG Tan, N Walley, L Pena, ... Genetics in Medicine 21 (1), 161-172, 2019 | 80 | 2019 |
A familial missense mutation in the hinge region of DAX1 associated with late-onset AHC in a prepubertal female P Bernard, L Ludbrook, G Queipo, MB Dinulos, GB Kletter, YH Zhang, ... Molecular genetics and metabolism 88 (3), 272-279, 2006 | 35 | 2006 |
A familial mutation in the testis-determining gene SRY shared by an XY female and her normal father. BK Jordan, D Frasier, E Vilain AMERICAN JOURNAL OF HUMAN GENETICS 69 (4), 619-619, 2001 | | 2001 |
A genome-wide spectrum of tandem repeat expansions in 338,963 humans Y Cui, W Ye, JS Li, JJ Li, E Vilain, T Sallam, W Li Cell 187 (9), 2336-2341. e5, 2024 | 3 | 2024 |
A link between gender identity and genes involved in sex hormone signalling V Harley, L Hare, K Balakrishnan, K York, J Erasmus, F Harte, E Vilain CLINICAL ENDOCRINOLOGY 89, 29-30, 2018 | | 2018 |
A minority of 46, XX true hermaphrodites are positive for the Y-DNA sequence including SRY K McElreavey, R Rappaport, E Vilain, N Abbas, F Richaud, S Lortat-Jacob, ... Human genetics 90, 121-125, 1992 | 118 | 1992 |
A novel approach for structural variant calling: Combining data from whole genome next-generation sequencing and optical mapping Y Porat, O Lev, M Einhorn, O Shani, E Vilain, HBS Barseghyan, ... 68th Annual Meeting of the American Society of Human Genetics,(October 16–20 …, 2018 | 1 | 2018 |
A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing MS Bramble, EH Goldstein, A Lipson, T Ngun, A Eskin, JE Gosschalk, ... Human Reproduction 31 (4), 905-914, 2016 | 88 | 2016 |
A Novel FSH Receptor (FSHR) Mutation Causing Primary Amenorrhea: A Fertility Application of Whole Exome Sequencing. EH Goldstein, MS Bramble, A Lipson, T Ngun, A Eskin, H Barseghyan, ... REPRODUCTIVE SCIENCES 23, 79A-80A, 2016 | | 2016 |
A practical approach to ambiguous genitalia in the newborn period SM Lambert, EJN Vilain, TF Kolon Urologic Clinics 37 (2), 195-205, 2010 | 68 | 2010 |
A recurrent de novo variant in NACC1 causes a syndrome characterized by infantile epilepsy, cataracts, and profound developmental delay K Schoch, L Meng, S Szelinger, DR Bearden, A Stray-Pedersen, OL Busk, ... The American Journal of Human Genetics 100 (2), 343-351, 2017 | 49 | 2017 |