Stephen Warren

Emory University, School of Medicine, Human Genetics

Publications

• 1.

  2013

  Donna M. McDonald-McGinn; Somayyeh Fahiminiya; Timothée Revil; Beata A. Nowakowska; Joshua Suhl; Alice Bailey; Elisabeth Mlynarski; David R. Lynch; Albert C. Yan; Larissa T. Bilaniuk; et al.

  Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.12Ds

  Journal of Medical Genetics. 2013;50(2):80-90.

• 2.

  2013

  Reid S. Alisch; Tao Wang; Pankaj Chopra; Jeannie Visootsak; Karen N. Conneely; Stephen T. Warren

  Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus

  BMC Medical Genetics. 2013;14(1).

• 3.

  2012

  Tao Wang; Qian Pan; Li Lin; Keith E. Szulwach; Chun-Xiao Song; Chuan He; Hao Wu; Stephen T. Warren; Peng Jin; Ranhui Duan; et al.

  Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum

  Human Molecular Genetics. 2012;21(26):5500-5510.

Journals

•  
  Publications
• American Journal of Human Genetics
  20
• Human Molecular Genetics
  16
• Nature Genetics
  12
• Genomics
  11
• Proceedings of the National Academy of Sciences of the United States of America
  9

Institutional Network

• Internal Organizations
  Shared Pub.
• School of Medicine, Radiation Oncology
  1

  

• External Organizations
  Shared Pub.
• Emory University School of Medicine
  96
• Emory University
  31
• Baylor College of Medicine
  13
• Howard Hughes Medical Institute
  6
• Greenwood Genetics Center
  5
• Michigan State University, College of Human Medicine
  5

Coauthor Network

• Internal Coauthors
  Shared Pub.
• Paula Vertino
  1

  

• External Coauthors
  Shared Pub.
• Peng Jin
  15
• David L Nelson
  15
• Fuping Zhang
  15
• Yue Feng
  12
• Jennifer G Mulle
  11
• Stephanie Ceman
  9