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Relationship Between ERCC1 Polymorphisms, Disease Progression, and Survival in the Gynecologic Oncology Group Phase III Trial of Intraperitoneal Versus Intravenous Cisplatin and Paclitaxel for Stage III Epithelial Ovarian Cancer

Journal of clinical oncology, 2008-07, Vol.26 (21), p.3598-3606

2008

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Genotype and Tumor Locus Determine Expression Profile of Pseudohypoxic Pheochromocytomas and Paragangliomas

Neoplasia (New York, N.Y.), 2013-04, Vol.15 (4), p.435-IN22

2013

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Coordinate up-regulation of TMEM97 and cholesterol biosynthesis genes in normal ovarian surface epithelial cells treated with progesterone: implications for pathogenesis of ovarian cancer

BMC cancer, 2007-12, Vol.7 (1), p.223-223, Article 223

2007

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Biochemically Silent Abdominal Paragangliomas in Patients with Mutations in the Succinate Dehydrogenase Subunit B Gene

The journal of clinical endocrinology and metabolism, 2008-12, Vol.93 (12), p.4826-4832

2008

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Genetics of Carney Triad: Recurrent Losses at Chromosome 1 but Lack of Germline Mutations in Genes Associated with Paragangliomas and Gastrointestinal Stromal Tumors

The journal of clinical endocrinology and metabolism, 2007-08, Vol.92 (8), p.2938-2943

2007

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Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria

Journal of human genetics, 2010-03, Vol.55 (3), p.182-185

2010

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Proportion of Heritable Paraganglioma Cases and Associated Clinical Characteristics

The Laryngoscope, 2001-10, Vol.111 (10), p.1822-1827

2001

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Analysis of CHEK2 gene for ovarian cancer susceptibility

Gynecologic oncology, 2004-10, Vol.95 (1), p.62-69

2004

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A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family

Neurogenetics, 2002-03, Vol.4 (1), p.43-53

2002

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Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation

Human genetics, 2001-08, Vol.109 (2), p.216-223

2001

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Genetics of familial paragangliomas: past, present, and future

Otolaryngologic clinics of North America, 2001-10, Vol.34 (5), p.863-879

Baysal, B E

2001

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Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss

Genes chromosomes & cancer, 2001-07, Vol.31 (3), p.255-263

2001

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High-resolution methylation analysis of the BRCA1 promoter in ovarian tumors

Cancer genetics and cytogenetics, 2005-06, Vol.159 (2), p.114-122

2005

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Repositioning the hereditary paraganglioma critical region on chromosome band 11q23

Human genetics, 1999-03, Vol.104 (3), p.219-225

1999

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Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23

American journal of human genetics, 1997, Vol.60 (1), p.121-132

1997

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Fine Mapping of the Split-Hand/Split-Foot Locus ( SHFM3) at 10q24: Evidence for Anticipation and Segregation Distortion

American journal of human genetics, 1999-06, Vol.64 (6), p.1646-1654

1999

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Genomic organization and precise physical location of protein phosphatase 2A regulatory subunit A beta isoform gene on chromosome band 11q23

Gene, 1998-09, Vol.217 (1), p.107-116

1998

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Bipolar affective disorder partially cosegregates with a balanced t(9;11)(p24;q23.1) chromosomal translocation in a small pedigree

American journal of medical genetics, 1998-02, Vol.81 (1), p.81-91

1998

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Factors preventing materno-fetal transmission of SARS-CoV-2

Placenta (Eastbourne), 2020-08, Vol.97, p.1-5

2020

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Relationship Between ERCC1 Polymorphisms, Disease Progression, and Survival in the Gynecologic Oncology Group Phase III Trial of Intraperitoneal Versus Intravenous Cisplatin and Paclitaxel for Stage III Epithelial Ovarian Cancer

Genotype and Tumor Locus Determine Expression Profile of Pseudohypoxic Pheochromocytomas and Paragangliomas

Coordinate up-regulation of TMEM97 and cholesterol biosynthesis genes in normal ovarian surface epithelial cells treated with progesterone: implications for pathogenesis of ovarian cancer

Biochemically Silent Abdominal Paragangliomas in Patients with Mutations in the Succinate Dehydrogenase Subunit B Gene

Genetics of Carney Triad: Recurrent Losses at Chromosome 1 but Lack of Germline Mutations in Genes Associated with Paragangliomas and Gastrointestinal Stromal Tumors

Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria

Proportion of Heritable Paraganglioma Cases and Associated Clinical Characteristics

Analysis of CHEK2 gene for ovarian cancer susceptibility

A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family

Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation

Genetics of familial paragangliomas: past, present, and future

Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss

High-resolution methylation analysis of the BRCA1 promoter in ovarian tumors

Repositioning the hereditary paraganglioma critical region on chromosome band 11q23

Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23

Fine Mapping of the Split-Hand/Split-Foot Locus ( SHFM3) at 10q24: Evidence for Anticipation and Segregation Distortion

Genomic organization and precise physical location of protein phosphatase 2A regulatory subunit A beta isoform gene on chromosome band 11q23

Bipolar affective disorder partially cosegregates with a balanced t(9;11)(p24;q23.1) chromosomal translocation in a small pedigree

Factors preventing materno-fetal transmission of SARS-CoV-2

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