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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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Genomic and Expression Analyses of Alternatively Spliced Transcripts of the MLL Septin-like Fusion Gene (MSF) That Map to a 17q25 Region of Loss in Breast and Ovarian Tumors

Genomics (San Diego, Calif.), 2000-01, Vol.63 (2), p.165-172

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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Understandings of Basic Genetics in the United States: Results from a National Survey of Black and White Men and Women

Public health genomics, 2010-01, Vol.13 (7/8), p.467-476

2010

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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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Characterisation and genetic mapping of a new X linked deafness syndrome

Journal of medical genetics, 2000-11, Vol.37 (11), p.836-841

2000

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Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22

Science (American Association for the Advancement of Science), 1992-11, Vol.258 (5085), p.1148-1152

1992

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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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Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma : implications for 9p tumor-suppressor gene(s)

American journal of human genetics, 1993-07, Vol.53 (1), p.96-104

1993

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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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Absence of PTEN Germ-Line Mutations in Men with a Potential Inherited Predisposition to Prostate Cancer

Clinical cancer research, 1999-06, Vol.5 (6), p.1387-1391

1999

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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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Questioning the need for anonymous genetic counseling and testing

American journal of human genetics, 1996-10, Vol.59 (4), p.968-970

1996

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Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag

Mammalian genome, 2001-12, Vol.12 (12), p.925-929

2001

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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

Genomic and Expression Analyses of Alternatively Spliced Transcripts of the MLL Septin-like Fusion Gene (MSF) That Map to a 17q25 Region of Loss in Breast and Ovarian Tumors

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

Understandings of Basic Genetics in the United States: Results from a National Survey of Black and White Men and Women

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

Characterisation and genetic mapping of a new X linked deafness syndrome

Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22

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

Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma : implications for 9p tumor-suppressor gene(s)

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

Absence of PTEN Germ-Line Mutations in Men with a Potential Inherited Predisposition to Prostate Cancer

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

Questioning the need for anonymous genetic counseling and testing

Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag

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