F. Li

D. Fairclough, J. Garber, L. Forétova, 1998, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms.

S. Friend, A. Look, J. Garber, 1992, The New England journal of medicine.

Nonlinkage of 16q markers to familial predisposition to Wilms' tumor.

M. Leppert, L. Strong, A. Reeve, 1992, Cancer research.

Outcome of pregnancy in survivors of Wilms' tumor.

S. Sallan, D. Green, F. Li, 1987, JAMA.

Classification and aetiology of the aplastic anaemias.

B. Alter, N. Potter, F. Li, 1978, Clinics in haematology.

Familial Barrett esophagus and adenocarcinoma of the gastroesophageal junction.

C. Eng, F. Li, S. Spechler, 1993, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.

Jeng-Shin Lee, F. Li, D. Yandell, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Prospective study of a family cancer syndrome.

J. Fraumeni, F. Li, F. Li, 1982, JAMA.

Germ-line p53 mutations predispose to a wide spectrum of early-onset cancers.

J. Fraumeni, J. Garber, D. Malkin, 2001, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

A cancer family syndrome in twenty-four kindreds.

W. Blattner, M. Tucker, J. Fraumeni, 1988, Cancer research.

Chromosome abnormalities in two benign adipose tumors.

F. Li, A. Sandberg, J. Limon, 1986, Cancer genetics and cytogenetics.

The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8.

F. Li, Frederick P. Li, N. Tanaka, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes.

F. Hecht, T. Glover, F. Li, 1988, Cancer genetics and cytogenetics.

Hereditary renal-cell carcinoma associated with a chromosomal translocation.

S. Jacobs, R. Brown, A. Cohen, 1979, The New England journal of medicine.

Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni Syndrome.

D. Sgroi, D. Haber, J. Garber, 2001, Cancer research.

Absence of germline p16 INK4a alterations in p53 wild type Li-Fraumeni syndrome families

C. Portwine, F. Li, D. Malkin, 2000, Journal of medical genetics.

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

J. Fraumeni, F. Li, J F Fraumeni, 1969, Annals of internal medicine.

Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome.

K. Isselbacher, J. Fraumeni, D. Haber, 1999, Science.

Follow-up study of twenty-four families with Li-Fraumeni syndrome.

J. Fraumeni, A. Goldstein, J. Garber, 1991, Cancer research.

Comprehensive mutational scanning of the p53 coding region by two-dimensional gene scanning.

C. Eng, J. Vijg, I. Sigalas, 1998, Carcinogenesis.

Erratum: Germ-line mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms (New England Journal of Medicine (May 14, 1992))

S. Friend, L. Strong, F. Li, 1997 .

Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma.

A. Gottlieb, L. Diller, E. Sexsmith, 1995, The Journal of clinical investigation.

Germ-line p53 mutations in 15 families with Li-Fraumeni syndrome.

S. Friend, J. Fraumeni, J. Garber, 1995, American journal of human genetics.

Acute myelocytic leukemia in two brothers with polyposis coli and carcinoma of the colon.

M. Greenberg, D. Marchetto, K. C. Anderson, 1981, Annals of internal medicine.

Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia.

F. Hecht, F. Li, B. Kaiser‐Mccaw, 1981, Cancer genetics and cytogenetics.

Mortality from second tumors among long-term survivors of retinoblastoma.

C. Eng, J. Seddon, N. Tarbell, 1993, Journal of the National Cancer Institute.

Histopathological, cytogenetic, and molecular characterization of renal cortical tumors.

S. Jhanwar, V. Reuter, W. Fair, 1991, Cancer research.

Molecular epidemiology study of a suspected community cluster of childhood cancers.

J. Fraumeni, S. Verselis, R. Hutchinson, 1997, Medical and pediatric oncology.

RB1 genetic testing as a clinical service: a follow-up study.

T. Dryja, L. Diller, K. B. Davis, 2001, Medical and pediatric oncology.

Cancer control in susceptible groups: opportunities and challenges.

F. Li, F. Li, 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Positional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpoint.

T. Glover, F. Li, R. Gemmill, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Bone sarcomas linked to radiotherapy and chemotherapy in children.

D M Green, R. Hoover, L. Strong, 1987, The New England journal of medicine.

The course of five-year survivors of cancer in childhood.

N. Jaffe, F. Li, M. Myers, 1978, The Journal of pediatrics.

Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma.

P. Cin, C. Turc‐Carel, F. Li, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Rhabdomyosarcoma in children: epidemiologic study and identification of a familial cancer syndrome.

J. Fraumeni, F. Li, J F Fraumeni, 1969, Journal of the National Cancer Institute.

Hereditary retinoblastoma and risk of lung cancer.

M. Tucker, R. Tarone, J. Seddon, 2000, Journal of the National Cancer Institute.

Translocation X;18 in synovial sarcoma.

P. Cin, C. Turc‐Carel, F. Li, 1986, Cancer genetics and cytogenetics.

Wilms tumor in five cousins.

L. Holmes, J. Cordero, P. Gerald, 1980, Pediatrics.

Progeny of childhood-cancer survivors.

N. Jaffe, F. Li, F. Li, 1974, Lancet.

Familial mesothelioma after intense asbestos exposure at home.

J. Lokich, E. W. Wilkins, F P Li, 1978, JAMA.

Germ-line msh6 mutations in colorectal cancer families.

J. Tytell, A. Ziogas, H. Anton-Culver, 1999, Cancer research.

Cancer mortality among chemists.

N. Mantel, J. Fraumeni, F. Li, 1969, Journal of the National Cancer Institute.

Cancer mortality among beekeepers.

J. McDonald, C. R. Mehta, F. Li, 1979, Journal of occupational medicine. : official publication of the Industrial Medical Association.

del(6q) as a possible primary change in malignant mesothelioma.

F. Li, A. Sandberg, A. Meloni, 1992, Cancer genetics and cytogenetics.

Chromosome 3 and 12p rearranged in a well-differentiated peritoneal mesothelioma.

A. Sandberg, H. Decker, H. Bixenman, 1990, Cancer genetics and cytogenetics.

Chromosome changes in malignant mesothelioma.

R. Stahel, F. Li, Frederick P. Li, 1986, Cancer genetics and cytogenetics.

A 1.5-megabase restriction map surrounding MYC does not include the translocation breakpoint in familial renal cell carcinoma.

F. Hecht, R. Gemmill, H. Drabkin, 1989, Genomics.

Abnormally banded region in a poorly differentiated sarcoma is not correlated with amplification of c-MYC or c-MOS protooncogenes.

F. Li, A. Sandberg, J. Limon, 1988, Cancer genetics and cytogenetics.

Mapping by chromosome sorting of several gene probes, including c-myc, to the derivative chromosomes of a 3;8 translocation associated with familial renal cancer.

S. Latt, C. Morton, F. Li, 1986, Cytometry.

Molecular epidemiology studies of cancer in families.

F. Li, F. Li, F. Li, 1993, British Journal of Cancer.

Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma.

B. Seizinger, N. Kley, L. Gelbert, 1994, American journal of human genetics.

Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein.

R. Weinberg, S. Friend, F. Li, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Kids who really shouldn't smoke.

J. Hanley, F. Li, G. E. Holmes, 1979, The New England journal of medicine.

Survival of children with cancer.

M. Mandelson, F. Li, F. Li, 1986, JAMA.

Offspring of patients treated for cancer in childhood.

N. Jaffe, F. Li, G. E. Holmes, 1979, Journal of the National Cancer Institute.

Hepatoblastoma and familial adenomatous polyposis.

L. Strong, J. Garber, H. Järvinen, 1988, Journal of the National Cancer Institute.

Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2.

M. Leppert, D. Gilliland, J. Aster, 1996, Blood.

Multiple primary cancers in families with Li-Fraumeni syndrome.

J. Fraumeni, J. Garber, Frederick P. Li, 1998, Journal of the National Cancer Institute.

Hereditary retinoblastoma, lipoma, and second primary cancers.

J. Fraumeni, R. Tarone, F. Li, 1997, Journal of the National Cancer Institute.

Cytogenetic analysis of soft tissue sarcomas. Recurrent chromosome abnormalities in malignant peripheral nerve sheath tumors (MPNST).

S. Jhanwar, F. Li, Frederick P. Li, 1994, Cancer genetics and cytogenetics.

Recommendations on predictive testing for germ line p53 mutations among cancer-prone individuals.

S. Friend, A. Patenaude, L. Strong, 1992, Journal of the National Cancer Institute.

Germline WT1 mutations in Wilms' tumor patients: preliminary results.

N. Breslow, J. Pelletier, D. Green, 1996, Medical and pediatric oncology.

Identification and management of inherited cancer susceptibility.

F. Li, Frederick P. Li, 1995, Environmental health perspectives.

Collaborative interdisciplinary studies of p53 and other predisposing genes in Li-Fraumeni syndrome.

J. Fraumeni, F. Li, F. Li, 1994, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Attitudes of 47 mothers of pediatric oncology patients toward genetic testing for cancer predisposition.

A. Patenaude, D. Fairclough, Laura A. Basili, 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Cancer incidence after retinoblastoma. Radiation dose and sarcoma risk.

J. Fraumeni, R. Tarone, M. Stovall, 1997, JAMA.

Third international workshop on collaborative interdisciplinary studies of p53 and other predisposing genes in Li-Fraumeni syndrome.

J. Fraumeni, C. Eng, F. Li, 1997, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Cancer in relatives of patients with aplastic anemia.

F. Li, N. Potter, C. Sarmousakis, 1983, Cancer genetics and cytogenetics.

Therapy-linked leukemia.

F. Li, D. Nathan, A. Walker, 1971, British medical journal.

Classical Fanconi anemia in a family with hypoplastic anemia.

N. Potter, F. Li, F. Li, 1978, The Journal of pediatrics.

A family with acute leukemia, hypoplastic anemia and cerebellar ataxia: association with bone marrow C-monosomy.

J. Whang‐Peng, G. Vawter, F. Li, 1978, The American journal of medicine.

Mechanism of tumorigenesis of renal carcinomas associated with the constitutional chromosome 3;8 translocation.

L. Schmidt, M. Wei, F. Chen, 1995, The cancer journal from Scientific American.

Asbestos-associated diseases in a cohort of cigarette-filter workers.

F. Li, Frederick P. Li, E. Gaensler, 1989, The New England journal of medicine.

The surgical management of hereditary multifocal renal carcinoma.

Frederick P. Li, S. Jacobs, R. Brown, 1981, The Journal of urology.

Interactions of cancer susceptibility genes and environmental carcinogens. American Association for Cancer Research (AACR)-International Agency for Research on Cancer (IARC) Joint Conference.

F. Li, R. Montesano, F. Li, 1994, Cancer research.

The region of common allelic losses in sporadic renal cell carcinoma is bordered by the loci D3S2 and THRB.

C. Wijmenga, F. Li, C. Buys, 1991, Genomics.

Carotid body tumors in humans: genetics and epidemiology.

L. Strong, S. Grufferman, J. Carney, 1982, Journal of the National Cancer Institute.

Hodgkin's Disease, tonsillectomy and family size.

F. Li, N. Gutensohn, R. Johnson, 1975, The New England journal of medicine.

Cancer families: human models of susceptibility to neoplasia--the Richard and Hinda Rosenthal Foundation Award lecture.

F. Li, F. Li, 1988, Cancer research.

Hepatoblastoma in families with polyposis coli.

J. Seddon, F. Li, G. E. Holmes, 1987, JAMA.

Childhood malignant melanoma. Incidence and etiology.

D. Green, F. Li, J. Bader, 1985, The American journal of pediatric hematology/oncology.

Hodgkin's Disease in Childhood: An Epidemiologic Study

J. Fraumeni, F. Li, F. Li, 1969 .

Acute leukemia after radiotherapy in a patient with Turcot's syndrome. Impaired colony formation in skin fibroblast cultures after irradiation.

J. Little, R. Mayer, M. Paterson, 1983, The American journal of medicine.

Endometrial carcinoma after Hodgkin disease in childhood.

F. Li, J. Cassady, G. Brown, 1980, Medical and pediatric oncology.

Childhood cancer in sibs.

M. Tucker, J. Fraumeni, F. Li, 1976, The Journal of pediatrics.

An endometrial stromal sarcoma with clonal cytogenetic abnormalities.

N. Weidner, A. Sandberg, C. Sreekantaiah, 1991, Cancer genetics and cytogenetics.

A case-control study of the etiology of Ewing's sarcoma.

D. Winn, J. Fraumeni, L. Robison, 1992, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Possible inherited leukaemogenic factors in familial acute myelogenous leukaemia.

E. Henderson, G. Todaro, A. Snyder, 1970, Lancet.

Second neoplasms after Wilms' tumor in childhood.

S. Sallan, D. Green, J. Cassady, 1983, Journal of the National Cancer Institute.

Hypertension in long-term survivors of childhood renal cancers.

S. Sallan, N. Tarbell, F. Li, 1989, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Translocation of c-myc in the hereditary renal cell carcinoma associated with a t(3;8)(p14.2;q24.13) chromosomal translocation.

D. Patterson, F. Li, H. Drabkin, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Acupuncture and possible hepatitis B infection.

E. Shiang, F. Li, F. Li, 1980, JAMA.

Cancer Families and Susceptibility to Cancer

F. Li, F. Li, 1991 .