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Eric Vilain
Eric Vilain
Professor of Human Genetics, UCLA
在 ucla.edu 的电子邮件经过验证
标题
引用次数
年份
" Sexual orientation, controversy, and science": Erratum.
JM Bailey, PL Vasey, LM Diamond, SM Breedlove, E Vilain, M Epprecht
Sage Publications, 2017
22017
“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
2772012
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
12005
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
802019
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
352006
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
32024
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
1181992
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
12018
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
882016
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
682010
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
492017
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