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MicroRNAs in development and disease

Clinical genetics, 2008-10, Vol.74 (4), p.296-306

2008

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Conquering the complex world of human septins: implications for health and disease

Clinical genetics, 2010-06, Vol.77 (6), p.511-524

2010

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PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma

Proceedings of the National Academy of Sciences - PNAS, 1991-11, Vol.88 (21), p.9638-9642

1991

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Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections

The American journal of cardiology, 1998-08, Vol.82 (4), p.474-479

1998

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Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas

Cancer research (Chicago, Ill.), 2001-05, Vol.61 (10), p.4130-4135

2001

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Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors

Cancer research (Chicago, Ill.), 2000-09, Vol.60 (17), p.4729-4734

2000

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Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines

Cancer letters, 2000-05, Vol.152 (2), p.193-199

2000

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Mutant deoxynucleotide carrier is associated with congenital microcephaly

Nature genetics, 2002-09, Vol.32 (1), p.175-179

2002

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A region of interstitial 17q25 allelic loss in ovarian tumors coincides with a defined region of loss in breast tumors

Oncogene, 1997-04, Vol.14 (16), p.1991-1994

1997

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Autosomal Dominant Stapes Ankylosis with Broad Thumbs and Toes, Hyperopia, and Skeletal Anomalies Is Caused by Heterozygous Nonsense and Frameshift Mutations in NOG, the Gene Encoding Noggin

American journal of human genetics, 2002-09, Vol.71 (3), p.618-624

2002

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Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland

American journal of human genetics, 1994-06, Vol.54 (6), p.1060-1066

1994

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FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors

Cytogenetics and cell genetics, 1996, Vol.72 (4), p.319

1996

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An Integrated Physical and Gene Map of Human Distal Chromosome 17q24–Proximal 17q25 Encompassing Multiple Disease Loci

Genomics (San Diego, Calif.), 1999-04, Vol.57 (1), p.36-42

1999

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Human dermatosparaxis : a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen

American journal of human genetics, 1992-08, Vol.51 (2), p.235-244

1992

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Virtual genome scan: a tool for restriction landmark-based scanning of the human genome

Genome research, 2001-08, Vol.11 (8), p.1453

2001

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BRCA1 mutation testing: controversies and challenges

Clinical chemistry (Baltimore, Md.), 1997-01, Vol.43 (1), p.6-8

1997

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miRNAs and cancer: New research developments and potential clinical applications

Cancer biology & therapy, 2009-12, Vol.8 (24), p.2317-2322

2009

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Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia

The Journal of pediatrics, 2000-12, Vol.137 (6), p.882-886

2000

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Mutations in the Slow Skeletal Muscle Fiber Myosin Heavy Chain Gene ( MYH7) Cause Laing Early-Onset Distal Myopathy (MPD1)

American journal of human genetics, 2004-10, Vol.75 (4), p.703-708

2004

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Risk Assessment and Presymptomatic Molecular Diagnosis in Hereditary Breast Cancer

Clinics in laboratory medicine, 1996-03, Vol.16 (1), p.139-167

1996

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Overexpressed genes/ESTs and characterization of distinct amplicons on 17q23 in breast cancer cells

Neoplasia (New York, N.Y.), 2001-11, Vol.3 (6), p.521-526

2001

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DNA diagnosis with mutation-specific artificial methylation sites: application to rapid screening of delta F508

Clinical chemistry (Baltimore, Md.), 1992-12, Vol.38 (12), p.2422

1992

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White Americans' Genetic Lay Theories of Race Differences and Sexual Orientation: Their Relationship with Prejudice toward Blacks, and Gay Men and Lesbians

Group processes & intergroup relations, 2006-01, Vol.9 (1), p.77-94

2006

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The Western New York Health Resources Project : developing access to local health information

Bulletin of the Medical Library Association, 1998-07, Vol.86 (3), p.335-339

1998

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Distal chromosome 17q loss in Barrett's esophageal and gastric cardia adenocarcinomas: Implications for tumorigenesis

Molecular carcinogenesis, 1998-08, Vol.22 (4), p.222-228

1998

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MicroRNAs in development and disease

Conquering the complex world of human septins: implications for health and disease

PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma

Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections

Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas

Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors

Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines

Mutant deoxynucleotide carrier is associated with congenital microcephaly

A region of interstitial 17q25 allelic loss in ovarian tumors coincides with a defined region of loss in breast tumors

Autosomal Dominant Stapes Ankylosis with Broad Thumbs and Toes, Hyperopia, and Skeletal Anomalies Is Caused by Heterozygous Nonsense and Frameshift Mutations in NOG, the Gene Encoding Noggin

Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland

FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors

An Integrated Physical and Gene Map of Human Distal Chromosome 17q24–Proximal 17q25 Encompassing Multiple Disease Loci

Human dermatosparaxis : a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen

Virtual genome scan: a tool for restriction landmark-based scanning of the human genome

BRCA1 mutation testing: controversies and challenges

miRNAs and cancer: New research developments and potential clinical applications

Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia

Mutations in the Slow Skeletal Muscle Fiber Myosin Heavy Chain Gene ( MYH7) Cause Laing Early-Onset Distal Myopathy (MPD1)

Risk Assessment and Presymptomatic Molecular Diagnosis in Hereditary Breast Cancer

Overexpressed genes/ESTs and characterization of distinct amplicons on 17q23 in breast cancer cells

DNA diagnosis with mutation-specific artificial methylation sites: application to rapid screening of delta F508

White Americans' Genetic Lay Theories of Race Differences and Sexual Orientation: Their Relationship with Prejudice toward Blacks, and Gay Men and Lesbians

The Western New York Health Resources Project : developing access to local health information

Distal chromosome 17q loss in Barrett's esophageal and gastric cardia adenocarcinomas: Implications for tumorigenesis

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