P. Watson

发表

BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes.

Giovanni Parmigiani, Susan G Hilsenbeck, Judy E Garber, 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Age-of-onset heterogeneity in hereditary breast cancer: Minimal clues for diagnosis

R. Fitzgibbons, H. Lynch, P. Watson, 1988, Breast Cancer Research and Treatment.

Clinical/genetic features in hereditary breast cancer

H. Lynch, P. Watson, T. Conway, 1990, Breast Cancer Research and Treatment.

Natural history and age at onset of hereditary breast cancer

H. Lynch, P. Watson, T. Conway, 1992, Cancer.

Monitoring High Risk Women: Psychological Aspects

H. Lynch, P. Watson, T. Conway, 1991 .

Mammography Screening in Women Under Age 50 Years

H. Lynch, P. Watson, T. Conway, 1988 .

Alleles of the APC gene: An attenuated form of familial polyposis

G. Thomas, P. Laurent-Puig, M. Robertson, 1993, Cell.

The tumor spectrum in HNPCC.

H. Lynch, P. Watson, 1994, Anticancer research.

Psychologic Aspects of Cancer Genetic Testing: A Research Update for Clinicians

H. Lynch, S. Tinley, P. Watson, 1997 .

Hereditary colorectal cancer.

H T Lynch, J F Lynch, T. Smyrk, 1991, Seminars in oncology.

Surfaced-Enhanced Laser Desorption/Ionization Time-of-Flight (SELDI-TOF) Differentiation of Serum Protein Profiles of BRCA-1 and Sporadic Breast Cancer

Lisa H. Cazares, O. John Semmes, L. Cazares, 2004, Annals of Surgical Oncology.

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

Robin J. Leach, Paul S. Meltzer, Jean Weissenbach, 1993, Cell.

Hereditary chronic lymphocytic leukemia: an extended family study and literature review.

D. Weisenburger, W. Sanger, H. Lynch, 2002, American journal of medical genetics.

Hereditary nonpolyposis colorectal cancer--Lynch syndromes I and II.

T. Smyrk, B. Boman, H. Lynch, 1988, Gastroenterology clinics of North America.

Recognition and treatment of patients with hereditary nonpolyposis colon cancer (Lynch syndromes I and II).

R. Fitzgibbons, T. Smyrk, H. Lynch, 1987, Annals of surgery.

Genetic and immunopathological findings in a lymphoma family.

D. Weisenburger, H. Lynch, P. Watson, 1989, British Journal of Cancer.

Hereditary ovarian cancer: Heterogeneity in age at onset

H. Lynch, P. Watson, T. Conway, 2010 .

Whole pelvic helical tomotherapy for locally advanced cervical cancer: technical implementation of IMRT with helical tomothearapy

G. Parmigiani, K. Kinzler, S. Gruber, 2009, Radiation oncology.

Familial B-cell chronic lymphocytic leukemia: analysis of cytogenetic abnormalities, immunophenotypic profiles, and immunoglobulin heavy chain gene usage.

W. Chan, D. Weisenburger, W. Sanger, 2007, American journal of clinical pathology.

Pathology and heredity of breast cancer in younger women.

D. Page, H. Lynch, P. Watson, 1994, Journal of the National Cancer Institute. Monographs.

Familial breast-ovarian cancer locus on chromosome 17q12-q23

G. Lenoir, S. Narod, H. Lynch, 1991, The Lancet.

Gynecologic Cancer as a “Sentinel Cancer” for Women With Hereditary Nonpolyposis Colorectal Cancer Syndrome

R. Broaddus, S. Syngal, H. Lynch, 2005, Obstetrics and gynecology.

Screening adherence in BRCA1/2 families is associated with primary physicians' behavior

H. Lynch, S. Tinley, P. Watson, 2004, American journal of medical genetics. Part A.

The clinical features of ovarian cancer in hereditary nonpolyposis colorectal cancer.

J. Mecklin, H. Järvinen, I. Bernstein, 2001, Gynecologic oncology.

Cumulative incidence of colorectal and extracolonic cancers in mlh1 and msh2 mutation carriers of hereditary nonpolyposis colorectal cancer

H. Lynch, P. Watson, J. Lynch, 2007, Journal of Gastrointestinal Surgery.

Colorectal cancer in hereditary breast cancer kindreds

H. Lynch, P. Watson, A. Thorson, 1999, Diseases of the colon and rectum.

Familial colon cancer in the Tel‐Aviv area and the influence of ethnic origin

Z. Fireman, W. Kimberling, A. Figer, 1987, Cancer.

Etiology, natural history, management and molecular genetics of hereditary nonpolyposis colorectal cancer (Lynch syndromes): genetic counseling implications.

H. Lynch, S. Tinley, C. Lerman, 1997, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Colorectal adenomas in the Lynch syndromes. Results of a colonoscopy screening program.

T. Smyrk, H. Lynch, P. Watson, 1990, Gastroenterology.

Brca2 hereditary breast cancer pathophenotype

P. Tonin, D. Page, G. Lenoir, 1997, Breast Cancer Research and Treatment.

Histology of prophylactically removed ovaries from BRCA1 and BRCA2 mutation carriers compared with noncarriers in hereditary breast ovarian cancer syndrome kindreds.

H. Lynch, P. Watson, M. Casey, 2000, Gynecologic oncology.

Effect of Vitamin D and Calcium Supplementation on Cancer Incidence in Older Women: A Randomized Clinical Trial

K. Baggerly, R. Recker, P. Watson, 2017, JAMA.

Intra-abdominal carcinomatosis after prophylactic oophorectomy in women of hereditary breast ovarian cancer syndrome kindreds associated with BRCA1 and BRCA2 mutations.

S. Narod, H. Lynch, P. Watson, 2005, Gynecologic oncology.

A breast-ovarian cancer susceptibility gene maps to chromosome 17q21.

P. O'Connell, R. White, G. Lenoir, 1993, American journal of human genetics.

Systemic cancer and the FAMMM syndrome.

H. Lynch, W. Bergman, H. Lynch, 1990, British Journal of Cancer.

Hereditary breast cancer and family cancer syndromes

G. Lenoir, S. Narod, H. Lynch, 2004, World Journal of Surgery.

Breast cancer and importance of zygosity determination in triplet sisters

H. Lynch, P. Watson, T. Conway, 2004, Breast Cancer Research and Treatment.

The Tumor Spectrum in the Lynch Syndrome

P. Watson, Bronson D. Riley, 2004, Familial Cancer.

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.

A. de la Chapelle, H. Meijers-Heijboer, A. Wagner, 2003, American journal of human genetics.

Microsatellite instability and expression of MLH1 and MSH2 in normal and malignant endometrial and ovarian epithelium in hereditary nonpolyposis colorectal cancer family members.

J. Knezetic, H. Lynch, P. Watson, 1999, Cancer genetics and cytogenetics.

Prevalence of extra-esophageal cancers in patients with Barrett's esophagus and esophageal adenocarcinoma.

A. Chak, H. Lynch, P. Watson, 2012, Tropical gastroenterology : official journal of the Digestive Diseases Foundation.

Mammography Screening in Women Under Age 50 Years

H. Lynch, P. Watson, T. Conway, 1988 .

Colorectal and extracolonic cancer variations in MLH1/MSH2 hereditary nonpolyposis colorectal cancer kindreds and the general population

H. Lynch, P. Watson, A. Thorson, 1998, Diseases of the colon and rectum.

Tumor variation in three extended Lynch syndrome II kindreds.

H. Lynch, P. Watson, J. Lynch, 1988, The American journal of gastroenterology.

Hereditary ovarian cancer. Heterogeneity in age at diagnosis

H. Lynch, P. Watson, B. Ponder, 1991, Cancer.

Cancer risk in mismatch repair gene mutation carriers

H. Lynch, P. Watson, 2004, Familial Cancer.

Families Evaluable by Linkage

K. Kinzler, B. Vogelstein, L. Aaltonen, 2007 .

Advances in Brief Genetic Instability of Microsatellites in Endometrial Carcinoma

J. Boyd, H. Lynch, Andrew, 2006 .

Adenoma follow-up in at-risk Lynch syndrome family members.

T. Smyrk, H. Lynch, P. Watson, 1993, Anticancer research.

Characteristics of small bowel carcinoma in hereditary nonpolyposis colorectal carcinoma

J. Mecklin, H. Järvinen, H. Lynch, 1998, Cancer.

The epidemiology of endometrial cancer in hereditary nonpolyposis colorectal cancer.

J. Jass, J. Mecklin, H. Lynch, 1994, Anticancer research.

History and molecular genetics of Lynch syndrome in family G: a century later.

J. Douglas, S. Gruber, H. Lynch, 2005, JAMA.

Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer

H. Lynch, S. Tinley, P. Watson, 1999, Cancer.

DNA screening for breast/ovarian cancer susceptibility based on linked markers. A family study.

G. Lenoir, S. Narod, H. Lynch, 1993, Archives of internal medicine.

Multiple HNPCC tumours: ask the family!

H. Lynch, P. Watson, 1998, Gut.

Antiproliferative effect of mismatched double-stranded RNA on fresh human tumor cells analyzed in a clonogenic assay.

D. Strayer, P. Watson, I. Brodsky, 1986, Journal of interferon research.

Increasing incidence of breast cancer in family with BRCA1 mutation

G. Lenoir, H. Lynch, S. Narod, 1993, The Lancet.

Histology of BRCA1-associated ovarian tumours

P. Tonin, G. Lenoir, H. Lynch, 1994, The Lancet.

Genetic counselling and hereditary breast/ ovarian cancer

H. Lynch, P. Watson, 1992, The Lancet.

Prognosis of BRCA1 hereditary breast cancer

H. Lynch, P. Watson, J. Marcus, 1998, The Lancet.

Surgical Strategies for Management of the Lynch Syndromes

R. Fitzgibbons, T. Smyrk, B. Boman, 1990 .

Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review.

C. Boland, T. Smyrk, H. Lynch, 1993, Gastroenterology.

Familial aggregation of carcinoma of the endometrium.

H. Lynch, R. Coleman, P. Watson, 1994, American journal of obstetrics and gynecology.

Phenotypic variation in colorectal adenoma/cancer expression in two families. Hereditary flat adenoma syndrome

T. Smyrk, H. Lynch, P. Lynch, 1990, Cancer.

Laryngeal carcinoma in a lynch syndrome II kindred

H. Lynch, P. Watson, J. Lynch, 1988, Cancer.

Lymphocyte recruitment into the tumor site is altered in patients with MSI-H colon cancer

Poonam K Sharma, S. Thibodeau, H. Lynch, 2009, Familial Cancer.

Hereditary breast cancer: Pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage

G M Lenoir, P. Tonin, D. Page, 1996, Cancer.

Hereditary Nonpolyposis Colorectal Cancer Patients Replication Errors in Benign and Malignant Tumors from

H T Lynch, K. Kinzler, B. Vogelstein, 2006 .

Symptom Priority Ranking in the Care of Gastroesophageal Reflux: A Review of 1,850 Cases

P. Watson, S. Mittal, C. Filipi, 2000, Digestive Diseases.

The risk of extra‐colonic, extra‐endometrial cancer in the Lynch syndrome

J. Mecklin, H. Järvinen, I. Bernstein, 2008, International journal of cancer.

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

H T Lynch, J. Mecklin, H. Lynch, 1999, Gastroenterology.

Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients

K. Kinzler, N. Papadopoulos, J. Jass, 1996, Nature Medicine.

Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy

K. Baggerly, D. Yoon, S. Scherer, 2008, Laboratory Investigation.

Evidence for the role of aberrant DNA methylation in the pathogenesis of Lynch syndrome adenomas

Li Lin, W. Grady, H. Lynch, 2007, International journal of cancer.

Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer

H. Lynch, S. Tinley, C. Lerman, 1999, Cancer.

Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer

H. Lynch, S. Tinley, C. Lerman, 1999 .

Downregulation of Death-Associated Protein Kinase 1 (DAPK1) in Chronic Lymphocytic Leukemia

D. Weisenburger, M. Grever, J. Byrd, 2007, Cell.

Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms–mismatch repair (MAPP‐MMR)

Stephen B Gruber, Hoda Anton-Culver, Jonathan L. Velasquez, 2008, Human mutation.

Male breast cancer in the hereditary nonpolyposis colorectal cancer syndrome

J. Boyd, H. Lynch, P. Borgen, 2004, Breast Cancer Research and Treatment.

Analysis of CHEK2 gene for ovarian cancer susceptibility.

M. Goodman, Y. Conley, F. Modugno, 2004, Gynecologic oncology.

BRCA1 and BRCA2 hereditary breast carcinoma phenotypes

D. Page, G. Lenoir, H. Lynch, 1997 .

Extracolonic cancer in hereditary nonpolyposis colorectal cancer.

H. Lynch, P. Watson, 1993, Cancer.

Genetic instability of microsatellites in endometrial carcinoma.

A. Berchuck, J. Boyd, J. Boyd, 1993, Cancer research.

Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry

M. Stacy, H. Lynch, C. Snyder, 2013, Familial Cancer.

A descriptive study of BRCA1 testing and reactions to disclosure of test results

P. Tonin, S. Narod, H. Lynch, 1997, Cancer.

Colorectal carcinoma survival among hereditary nonpolyposis colorectal carcinoma family members

T. Smyrk, H. Lynch, P. Watson, 1998, Cancer.

Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancer

A. Wagner, B. Riley, R. Fodde, 2003, Journal of medical genetics.

Differential diagnosis of hereditary nonpolyposis colorectal cancer (Lynch syndrome I and Lynch syndrome II)

T. Smyrk, H. Lynch, P. Watson, 1988, Diseases of the colon and rectum.

Tumor‐infiltrating lymphocytes are a marker for microsatellite instability in colorectal carcinoma

T. Smyrk, H. Lynch, P. Watson, 2001, Cancer.

TGFBR1*6A may contribute to hereditary colorectal cancer.

A. de la Chapelle, B. Pasche, J. Baron, 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Tobacco use and increased colorectal cancer risk in patients with hereditary nonpolyposis colorectal cancer (Lynch syndrome).

H. Lynch, P. Watson, H. Roy, 2004, Archives of internal medicine.

The risk of endometrial cancer in hereditary nonpolyposis colorectal cancer.

J. Mecklin, H. Järvinen, H. Lynch, 1994, The American journal of medicine.

Natural history of colorectal cancer in hereditary nonpolyposis colorectal cancer (Lynch syndromes I and II)

H. Lynch, P. Watson, J. Marcus, 1988, Diseases of the colon and rectum.

Clinical nuances of Lynch syndromes I and II.

R. Fitzgibbons, T. Smyrk, H. Lynch, 1988, Progress in clinical and biological research.

Extracolonic cancer in hereditary nonpolyposis colorectal cancer

H. Lynch, P. Watson, 1993 .

Hereditary nonpolyposis colorectal cancer (Lynch syndromes I & II). Genetics, pathology, natural history, and cancer control, Part I.

T. Smyrk, B. Boman, H. Lynch, 1991, Cancer genetics and cytogenetics.

Breast cancer risk after bilateral prophylactic oophorectomy in BRCA1 mutation carriers.

O. Olopade, T. Rebbeck, A. Levin, 1999, Journal of the National Cancer Institute.

Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer

H. Lynch, S. Tinley, P. Watson, 1999 .

Prophylactic oophorectomy in inherited breast/ovarian cancer families.

B. Ponder, J. Struewing, D. Easton, 1995, Journal of the National Cancer Institute. Monographs.

Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome

J. Boyd, H. Lynch, P. Watson, 1996, Cancer.

An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer.

G. Lenoir, S. Narod, H. Lynch, 1999, Cancer genetics and cytogenetics.

Hereditary Ovarian Cancer: A Clinicopathological Study

H. Lynch, P. Watson, C. Bewtra, 1992, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

A nonsense mutation in MLH1 causes exon skipping in three unrelated HNPCC families.

S. Lipkin, A. Wagner, R. Fodde, 2001, Cancer research.

Epidemiology and Risk Factors

H. Lynch, P. Watson, J. Lynch, 1989, Clinical obstetrics and gynecology.

Breast cancer family history as a risk factor for early onset breast cancer

Jane Lynch, Henry T. Lynch, H. Lynch, 1988, Breast Cancer Research and Treatment.

Extremely early onset hereditary breast cancer (HBC): surveillance/management implications.

R. Fitzgibbons, H. Lynch, P. Watson, 1988, The Nebraska medical journal.

hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.

K. Kinzler, B. Vogelstein, A. de la Chapelle, 1994, Cancer research.

Correlations between esophageal diseases and manometric length: A study of 617 patients

P. Watson, C. Filipi, Z. Awad, 1999, Journal of Gastrointestinal Surgery.

Comparison of Extended Colectomy and Limited Resection in Patients With Lynch Syndrome

H. Lynch, N. Natarajan, P. Watson, 2010, Diseases of the colon and rectum.

Cumulative incidence of metachronous colorectal cancer

P. Watson, A. Thorson, Rebecca L. Cali, 1993, Diseases of the colon and rectum.

Risk of colon cancer in hereditary non-polyposis colorectal cancer patients as predicted by fuzzy modeling: Influence of smoking.

David D Jones, Hemant K Roy, R. Brand, 2006, World journal of gastroenterology.

Familial pancreatic cancer: clinicopathologic study of 18 nuclear families.

T. Smyrk, H. Lynch, P. Watson, 1990, The American journal of gastroenterology.

Phenotypic heterogeneity in multiple myeloma families.

D. Weisenburger, O. Olopade, W. Sanger, 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

The genetic epidemiology of male breast carcinoma

S. Narod, H. Lynch, P. Watson, 1999, Cancer.

Role for the Epidermal Growth Factor Receptor in Chemotherapy-Induced Alopecia

P. Watson, T. Malouff, L. Hansen, 2013, PloS one.

Detecting BRCA2 protein truncation in tissue biopsies to identify breast cancers that arise in BRCA2 gene mutation carriers.

H. Lynch, J. Holt, C. Snyder, 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Helicobacter pylori and Gastroduodenal Secretory Function

E. Gabrielson, R. Lothe, V. Reuter, 1996 .

Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage.

A. Chapelle, K. Kinzler, B. Vogelstein, 1994, American journal of human genetics.

A positive feedback loop between HER2 and ADAM12 in human head and neck cancer cells increases migration and invasion

P. Watson, C. Deng, V. Rao, 2011, Oncogene.

SELDI-TOF Serum Profiling for Prognostic and Diagnostic Classification of Breast Cancers

O. John Semmes, Roger R. Perry, George L. Wright, 2004, Disease markers.

Aspirin Use is Associated with Lower Prostate Cancer Risk in Male Carriers of BRCA Mutations

Carrie Snyder, H. Lynch, C. Snyder, 2014, Journal of Genetic Counseling.

AFAP: variety is the spice of life

H. Lynch, P. Watson, 1998, Gut.

Epidemiologic characteristics of the flat adenoma of muto

T. Smyrk, H. Lynch, P. Watson, 1992, Diseases of the colon and rectum.

Hereditary flat adenoma syndrome: A variant of familial adenomatous polyposis?

T. Smyrk, H. Lynch, P. Lynch, 1992, Diseases of the colon and rectum.

Colon cancer genetics

B. Vogelstein, C. Boland, T. Smyrk, 1992, Cancer.

Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.

T. Smyrk, H. Lynch, Raymond White, 1992, American journal of human genetics.

Familial and Genetic Factors — New Evidence

H. Lynch, P. Watson, J. Marcus, 1989 .

Histologic Features of Hereditary Nonpolyposis Colorectal Carcinoma

T. Smyrk, H. Lynch, P. Watson, 1990 .

Surveillance in Lynch syndrome: how aggressive?

T. Smyrk, H. Lynch, P. Watson, 1994, The American journal of gastroenterology.

Surveillance in hereditary nonpolyposis colorectal cancer: An international cooperative study of 165 families

J. Mecklin, J. Utsunomiya, H. Lynch, 1993, Diseases of the colon and rectum.

Accuracy of MSI testing in predicting germline mutations of MSH2 and MLH1: a case study in Bayesian meta-analysis of diagnostic tests without a gold standard.

Giovanni Parmigiani, G. Parmigiani, Sining Chen, 2005, Biostatistics.

Association between rectal optical signatures and colonic neoplasia: potential applications for screening.

Vadim Backman, Young L. Kim, Mohammed Jameel, 2009, Cancer research.

Medical genetic study of eight pancreatic cancer-prone families.

T. Smyrk, H. Lynch, P. Watson, 1995, Cancer investigation.

Historical and Natural Cancer History Facets of the Lynch Syndromes

R. Fitzgibbons, T. Smyrk, B. Boman, 1990 .

Colonoscopy Findings in a Series of Patients with Hereditary Colorectal Cancer

R. Fitzgibbons, T. Smyrk, H. Lynch, 1990 .

Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry

M. Stacy, H. Lynch, C. Snyder, 2013, Familial Cancer.

Medical/Legal Concerns in the Management of Patients from Lynch Syndromes Kindreds

H. Lynch, P. Lynch, P. Watson, 1990 .

Is analysis of lower esophageal sphincter vector volumes of value in diagnosing gastroesophageal reflux disease?

Christopher L. Perdue, P. Watson, C. Filipi, 2003, World journal of gastroenterology.

Neoplasia : Potential Applications for Screening Association between Rectal Optical Signatures and Colonic

Young L. Kim, Andrew J. Gomes, V. Backman, 2009 .

Mutation of a mutL homolog in hereditary colon cancer.

R. Fleischmann, M. Adams, J. Venter, 1994, Science.

Extracolonic cancer in hereditary nonpolyposis colorectal cancer

H. Lynch, P. Watson, 1993, Cancer.

A clinical, histopathological, and genetic study of Avellino corneal dystrophy in British families

A. Wagner, S. Bhattacharya, I. Cree, 2003, Journal of medical genetics.

Hereditary Colorectal Cancer

R. Fitzgibbons, T. Smyrk, B. Boman, 1990, Springer Japan.

Hereditary ovarian cancer: Heterogeneity in age at diagnosis

H. Lynch, P. Watson, B. Ponder, 1991 .

Advances in Brief HMSH 2 Mutations in Hereditary Nonpolyposis Colorectal Cancer Kindreds 1

A. Chapelle, K. Kinzler, B. Vogelstein, 2006 .

Mammography and hereditary breast cancer

H. Lynch, P. Watson, 2005, Breast Cancer Research and Treatment.

Hereditary breast cancer: Search for biomarkers

G. Merlo, J. Schlom, R. Callahan, 1987 .

The risk of extra‐colonic, extra‐endometrial cancer in the Lynch syndrome

J. Mecklin, H. Järvinen, I. Bernstein, 2008, International journal of cancer.

Early age at breast cancer onset--a genetic and oncologic perspective.

H. Lynch, P. Watson, 1990, American journal of epidemiology.