Teare

Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis

*American Journal of Human Genetics* 2003; 73(4):791-800

Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13

*American Journal of Human Genetics* 2003; 73(1):198-204

Two percent of men with early-onset prostate cancer harbor germline mutations in the BRCA2 gene

*American Journal of Human Genetics* 2003; 72(1):1-12

Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness

*Journal of Neurology, Neurosurgery & Psychiatry* 2002; 73(6):762-765

The gene for juvenile hyaline fibromatosis maps to chromosome 4q21

*American Journal of Human Genetics* 2002; 71(4):975-980

Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium

*Proceedings of the National Academy of Sciences of the United States of America* 2002; 99(2):827-831

Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12

*Kidney International* 2001; 60(4):1233-1239

Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14

*American Journal of Human Genetics* 2001; 68(5):1270-1276

Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13

*Medical and Pediatric Oncology* 2000; 35(6):526–530

The extent of linkage disequilibrium in four populations with distinct demographic histories

*Am J Hum Genet* 2000; 67:1544-54