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Rahman N

Multi-stage genome-wide association study identifies new susceptibility locus for testicular germ cell tumour on chromosome 3q25
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer
A genome-wide association study of testicular germ cell tumor
Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis
Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13
Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness
The gene for juvenile hyaline fibromatosis maps to chromosome 4q21
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
Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12
Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14
Linkage analysis of 56 multiplex families excludes the Cowden disease genePTEN as a major contributor to familial breast cancer

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