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3 Article(s) on File
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Reduced transcript expression of genes affected by inherited and de novo CNVs in autism
Nord AS,
Roeb W,
Dickel DE,
Walsh T,
Kusenda M,
OConnor KL,
Malhotra D,
McCarthy SE,
Stray SM,
Taylor SM,
Sebat J,
King B,
King MC,
McClellan JM

European Journal of Human Genetics
  19 (6): 727-731; Jun 2011   Elsevier PMC3110052
[Abstract]
[DOI]

Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51
Walsh T,
Pierce SB,
Lenz DR,
Brownstein Z,
Dagan-Rosenfeld O,
Shahin H,
Roeb W,
McCarthy SE,
Nord AS,
Gordon CR,
Ben-Neriah Z,
Sebat J,
Kanaan M,
Lee MK,
Frydman M,
King MC,
Avraham KB

American Journal of Human Genetics
  87 (1): 101-109 ; Jul 9 2010   PMCID: PMC2896780
[Abstract]
[DOI] [Full Text] [PDF]

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
Walsh T,
McClellan JM,
McCarthy SE,
Addington AM,
Pierce SB,
Cooper GM,
Nord AS,
Kusenda M,
Malhotra D,
Bhandari A,
Stray SM,
Rippey CF,
Roccanova P,
Makarov V,
Lakshmi B,
Findling RL,
Sikich L,
Stromberg T,
Merriman B,
Gogtay N,
Butler P,
Eckstrand K,
Noory L,
Gochman P,
Long R,
Chen Z,
Davis S,
Baker C,
Eichler EE,
Meltzer PS,
Nelson SF,
Singleton AB,
Lee MK,
Rapoport JL,
King MC,
Sebat J

Science
  320 (5875): 539-43; Apr 25 2008  
[Abstract]
[DOI] [Full Text] [PDF]


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