Eric Vilain

Research.com Recognitions

• 2011 - E. Mead Johnson Award, Society for Pediatric Research

Overview

Best Publications

• Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders

  Hane Lee;Joshua L. Deignan;Naghmeh Dorrani;Samuel P. Strom

  1042
  Citations

• Epigenetic Predictor of Age

  Sven Bocklandt;Wen Lin;Mary E. Sehl;Francisco J. Sánchez

  984
  Citations

• Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation

  Kristi Kerkel;Alexandra Spadola;Eric Yuan;Jolanta Kosek

  510
  Citations

• The genetics of sex differences in brain and behavior.

  Tuck C. Ngun;Negar Ghahramani;Francisco J. Sánchez;Sven Bocklandt

  460
  Citations

• Sexually dimorphic gene expression in mouse brain precedes gonadal differentiation

  Phoebe Dewing;Tao Shi;Steve Horvath;Eric Vilain

  439
  Citations

• Up-Regulation of WNT-4 Signaling and Dosage-Sensitive Sex Reversal in Humans

  Brian K. Jordan;Mansoor Mohammed;Saunders T. Ching;Emmanuèle Délot

  413
  Citations

• Direct Regulation of Adult Brain Function by the Male-Specific Factor SRY

  Phoebe Dewing;Charleston W K Chiang;Kevin Sinchak;Helena Sim

  394
  Citations

• Identification of SOX3 as an XX male sex reversal gene in mice and humans

  Edwina Sutton;James Hughes;Stefan John White;Ryohei Sekido

  301
  Citations

• Mutant Cohesin in Premature Ovarian Failure

  Sandrine Caburet;Valerie A. Arboleda;Elena Llano;Paul A. Overbeek

  300
  Citations

• Androgen Receptor Repeat Length Polymorphism Associated with Male-to-Female Transsexualism

  Lauren May Hare;Pascal Bernard;Francisco J Sanchez;Paul N Baird

  294
  Citations

• Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts

  Laure Frésard;Craig Smail;Nicole M. Ferraro;Nicole A. Teran

  268
  Citations

• Collective self-esteem as a coping resource for male-to-female transsexuals.

  Francisco J. Sánchez;Eric Vilain

  267
  Citations

• Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia.

  Brent L. Fogel;Hane Lee;Joshua L. Deignan;Samuel P. Strom

  258
  Citations

• Wnt4 overexpression disrupts normal testicular vasculature and inhibits testosterone synthesis by repressing steroidogenic factor 1/β-catenin synergy

  Brian K. Jordan;Jennifer H.-C. Shen;Robert Olaso;Holly A. Ingraham

  231
  Citations

• Summary of Consensus Statement on Intersex Disorders and Their Management

  Christopher P. Houk;Ieuan A. Hughes;S. Faisal Ahmed;Peter A. Lee

  226
  Citations

• Exome sequencing for the diagnosis of 46,XY disorders of sex development.

  Ruth M. Baxter;Valerie A. Arboleda;Hane Lee;Hayk Barseghyan

  223
  Citations

• Dimerization of SOX9 is required for chondrogenesis, but not for sex determination

  Pascal Bernard;Paisu Tang;Siyuan Liu;Phoebe Dewing

  208
  Citations

• DSDs: genetics, underlying pathologies and psychosexual differentiation

  Valerie A. Arboleda;David E. Sandberg;Eric Vilain

  205
  Citations

• Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome

  Valerie A Arboleda;Hane Lee;Rahul Parnaik;Alice Fleming

  189
  Citations

• MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.

  Julia Wang;Rami Al-Ouran;Yanhui Hu;Seon-Young Kim

  189
  Citations