A. Whelan

J. Moley, L. Manwaring, A. Whelan, 2011, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Evaluation of the family history collection process and the accuracy of cancer reporting among a series of women with endometrial cancer.

J. Ivanovich, P. Goodfellow, D. Mutch, 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.

Clustering of Lynch syndrome malignancies with no evidence for a role of DNA mismatch repair.

S. Thibodeau, P. Goodfellow, D. Mutch, 2008, Gynecologic oncology.

Genetics in the Clinic: Clinical, Ethical, and Social Implications for Primary Care

A. Whelan, 2001, Annals of Internal Medicine.

Human telomerase RNA mutations and bone marrow failure

J. Ivanovich, P. Goodfellow, David B. Wilson, 2003, The Lancet.

Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocation.

R. Steiner, F. Porter, M. Watson, 1995, American journal of medical genetics.

Structural organization and regulatory regions of the human medium-chain acyl-CoA dehydrogenase gene.

D. Kelly, A. Strauss, J. J. Kim, 1992, Biochemistry.

Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency.

Zhifang, G. Bellus, N. Gregersen, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Genetic/familial high-risk assessment: breast and ovarian, version 1.2014.

S. Friedman, K. Offit, S. Buys, 2014, Journal of the National Comprehensive Cancer Network : JNCCN.

Mapping human telomere regions with YAC and P1 clones: chromosome-specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regions.

A. Jauch, D. Smoller, C. Helms, 1996, Genomics.

Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.

P. Goodfellow, D. Mutch, J. Rader, 2004, American journal of human genetics.

Atypical clustering of gynecologic malignancies: A family study including molecular analysis of candidate genes.

P. Goodfellow, D. Mutch, J. Rader, 2000, Gynecologic oncology.

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.

Kenneth Offit, Elizabeth Swisher, Seema Khan, 2016, Journal of the National Comprehensive Cancer Network : JNCCN.

Mutations in the GGCX and ABCC6 genes in a family with pseudoxanthoma elasticum-like phenotypes.

Nicole L. Armstrong, J. Uitto, L. Schurgers, 2009, The Journal of investigative dermatology.

Revisiting the Role of Genetics Assessment among Patients Evaluated in a Colorectal Surgery Practice

J. Ivanovich, A. Whelan, 2004 .

Human Glucagon-Like Peptide-1 Receptor Gene in NIDDM: Identification and Use of Simple Sequence Repeat Polymorphisms in Genetic Analysis

M. Permutt, H. Donis-Keller, Y. Tanizawa, 1994, Diabetes.

An 11-year-old boy with mosaic ring chromosome 6 and dilated aortic root.

J. Ivanovich, M. Watson, A. Whelan, 2001, American journal of medical genetics.

MSI in endometrial carcinoma: Absence of MLH1 promoter methylation is associated with increased familial risk for cancers

J. Ivanovich, P. Goodfellow, J. Rader, 2002, International journal of cancer.

Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability

J. Ivanovich, P. Goodfellow, S. Wells, 1997, Genes, chromosomes & cancer.

Prophylactic oophorectomy and ovarian cancer surveillance. Patient perceptions and satisfaction.

E. Swisher, D. Mutch, J. Rader, 2001, The Journal of reproductive medicine.

Plexiform neurofibromatosis of the liver: Case report and review of the literature

S. Teefey, R. Ghalib, P. Huettner, 1995, Hepatology.

Qualitative Evaluation of Medical Information Processing Needs of 60 Women Choosing Ovarian Cancer Surveillance or Prophylactic Oophorectomy

E. Swisher, D. Mutch, J. Rader, 2002, Journal of Genetic Counseling.

Prophylactic oophorectomy and ovarian cancer surveillance

E. Swisher, J. Rader, A. Whelan, 2001 .

Genetic/familial high-risk assessment

L. Esserman, S. Friedman, K. Offit, 2010 .

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version

K. Offit, S. Buys, Rashmi Kumar, 2014 .

Genetics of Progressive Hearing Loss

A. Whelan, A. Hing, 1995 .

Genetic/familial high-risk assessment: breast and ovarian, version 1.2014.

S. Friedman, K. Offit, S. Buys, 2014, Journal of the National Comprehensive Cancer Network : JNCCN.

Genetic red flags: clues to thinking genetically in primary care practice.

P. Ganschow, R. Hopkin, J. Stallworth, 2004, Primary care.

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.

S. Friedman, K. Offit, S. Buys, 2016, Journal of the National Comprehensive Cancer Network : JNCCN.

DICER1 Mutations in Familial Pleuropulmonary Blastoma

Gretchen M. Williams, J. Ivanovich, P. Goodfellow, 2009, Science.