D Walsh

On familial factors in the attentional deficit in schizophrenia: a review and report of two new subject samples.

A F Mirsky, S. Kugelmass, K. Kendler, 1992, Journal of psychiatric research.

No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF)

B. Neale, K. Kendler, B. Riley, 2004, Molecular Psychiatry.

Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families

K. Kendler, D. Walsh, X. Wang, 2004, Molecular Psychiatry.

The Roscommon Family Study. I. Methods, diagnosis of probands, and risk of schizophrenia in relatives.

K. Kendler, D. Walsh, K S Kendler, 1993, Archives of general psychiatry.

Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families.

P. Sullivan, K. Kendler, B. Riley, 2003, Molecular Psychiatry.

Meta-analysis of 32 genome-wide linkage studies of schizophrenia

E M Wijsman, G Kalsi, T Sigmundsson, 2009, Molecular Psychiatry.