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Next-Generation Sequencing for Inherited Breast Cancer Risk: Counseling through the Complexity

Current oncology reports, 2014-03, Vol.16 (3), p.371-371, Article 371

2014

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Genetic testing in the clinical care of patients with pheochromocytoma and paraganglioma

Current opinion in endocrinology, diabetes, and obesity, 2014-06, Vol.21 (3), p.166-176

2014

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Genetic Diagnosis of Primary Immune Deficiencies

Immunology and allergy clinics of North America, 2008-05, Vol.28 (2), p.387-412

2008

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Evidence That the pre-mRNA Splicing Factor Clf1p Plays a Role in DNA Replication in Saccharomyces cerevisiae

Genetics (Austin), 2002-04, Vol.160 (4), p.1319-1333

2002

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Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study

Genetics in medicine, 2017-07, Vol.19 (7), p.787-795

2017

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Initial results of a prospective, multicenter trial to study inherited lung cancer risk associated with germline EGFR T790M: INHERIT EGFR

Journal of clinical oncology, 2015-05, Vol.33 (15_suppl), p.1505-1505

2015

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Cancer patients’ preferences for return of somatic and germline whole-exome sequencing results: Data from the CANSEQ study

Journal of clinical oncology, 2014-05, Vol.32 (15_suppl), p.1535-1535

2014

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Investigating hereditary risk from T790M (inherit): A prospective multicentered study of risk associated with germ-line EGFR T790M

Journal of clinical oncology, 2013-05, Vol.31 (15_suppl), p.TPS1606-TPS1606

2013

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Evidence that the pre-mRNA splicing factor Clf1p plays a role in DNA replication in Sacccharomyces cerevisiae

Genetics (Austin), 2002-04, Vol.160 (4), p.1319

2002

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Genetic Diagnosis of Primary Immune Deficiencies: Immunodeficiency Disorders

Immunology and allergy clinics of North America, 2008, Vol.28 (2)

2008

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Breakpoints and junctional regions of intragenic deletions in the HPRT gene in human T-Cells

Somatic cell and molecular genetics, 1995-09, Vol.21 (5), p.309-326

1995

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Development of long PCR techniques to analyze deletion mutations of the human hprt gene

Mutation research, 1998-07, Vol.403 (1), p.171-175

1998

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Germline EGFR Mutations and Familial Lung Cancer

Journal of clinical oncology, 2023-12, Vol.41 (34), p.5274-5284

2023

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Abstract 2417: The INHERIT EGFR study: Investigating hereditary risk from T790M

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.2417-2417

2013

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Next-Generation Sequencing for Inherited Breast Cancer Risk: Counseling through the Complexity

Genetic testing in the clinical care of patients with pheochromocytoma and paraganglioma

Genetic Diagnosis of Primary Immune Deficiencies

Evidence That the pre-mRNA Splicing Factor Clf1p Plays a Role in DNA Replication in Saccharomyces cerevisiae

Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study

Initial results of a prospective, multicenter trial to study inherited lung cancer risk associated with germline EGFR T790M: INHERIT EGFR

Cancer patients’ preferences for return of somatic and germline whole-exome sequencing results: Data from the CANSEQ study

Investigating hereditary risk from T790M (inherit): A prospective multicentered study of risk associated with germ-line EGFR T790M

Evidence that the pre-mRNA splicing factor Clf1p plays a role in DNA replication in Sacccharomyces cerevisiae

Genetic Diagnosis of Primary Immune Deficiencies: Immunodeficiency Disorders

Breakpoints and junctional regions of intragenic deletions in the HPRT gene in human T-Cells

Development of long PCR techniques to analyze deletion mutations of the human hprt gene

Germline EGFR Mutations and Familial Lung Cancer

Exome sequencing reveals recurrent germ line variants in patients with familial Waldenström macroglobulinemia

Abstract 2417: The INHERIT EGFR study: Investigating hereditary risk from T790M

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