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Research

MEIS1 in conferring sleep abnormalities and impaired cerebellar development" > Cross-species variant-to-function analyses implicate MEIS1 in conferring sleep abnormalities and impaired cerebellar development

  • Amber J. Zimmerman
  • Erika Almeraya Del Valle
  • Matthew C. Pahl
  • Fusun Doldur-Balli
  • Brendan T. Keenan
  • Patrick Z. Liu Zoe Y. Shetty Trisha R. Tsundupalli Justin Palermo Anitra Krishnan James A. Pippin Andrew D. Wells Olivia J. Veatch Alessandra Chesi
  • ... [+9 authors] ...,
  • Philip R. Gehrman
  • Alex C. Keene
  • Allan I. Pack
  • Struan F.A. Grant
  • First Published July 30, 2026
Resource

High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications

  • Tamim H. Shaikh
  • Xiaowu Gai
  • Juan C. Perin
  • Joseph T. Glessner
  • Hongbo Xie
  • Kevin Murphy Ryan O'Hara Tracy Casalunovo Laura K. Conlin Monica D'Arcy Edward C. Frackelton Elizabeth A. Geiger Chad Haldeman-Englert Marcin Imielinski Cecilia E. Kim Livija Medne Kiran Annaiah Jonathan P. Bradfield Elvira Dabaghyan Andrew Eckert Chioma C. Onyiah Svetlana Ostapenko F. George Otieno Erin Santa Julie L. Shaner Robert Skraban Ryan M. Smith Josephine Elia Elizabeth Goldmuntz Nancy B. Spinner Elaine H. Zackai Rosetta M. Chiavacci Robert Grundmeier
  • ... [+28 authors] ...,
  • Eric F. Rappaport
  • Struan F.A. Grant
  • Peter S. White
  • Hakon Hakonarson
  • First Published July 10, 2009
Methods

PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

  • Kai Wang
  • Mingyao Li
  • Dexter Hadley
  • Rui Liu
  • Joseph Glessner
  • Struan F.A. Grant
  • Hakon Hakonarson
  • Maja Bucan
  • First Published October 5, 2007
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