Published in Genes Chromosomes Cancer on November 01, 1995
Analysis of the 10q23 chromosomal region and the PTEN gene in human sporadic breast carcinoma. Br J Cancer (1999) 1.54
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3. Br J Cancer (1999) 1.06
Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour. Br J Cancer (1998) 1.05
A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH. Oncogene (2006) 1.01
Deletion mapping of chromosome 16q in hepatocellular carcinoma. Br J Cancer (1999) 0.97
Exclusion of BBC1 and CMAR as candidate breast tumour-suppressor genes. Br J Cancer (1997) 0.88
Chromosome band 16q24 is frequently deleted in human gastric cancer. Br J Cancer (1999) 0.84
A screen for germline mutations in the gene encoding CCCTC-binding factor (CTCF) in familial non-BRCA1/BRCA2 breast cancer. Breast Cancer Res (2004) 0.77
Localization of the gene for Cowden disease to chromosome 10q22-23. Nat Genet (1996) 3.53
WNT pathway and mammary carcinogenesis: loss of expression of candidate tumor suppressor gene SFRP1 in most invasive carcinomas except of the medullary type. Oncogene (2001) 2.32
Mutations of the human PTEN gene. Hum Mutat (2000) 2.11
Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors. Cancer Res (1997) 2.06
A refined molecular taxonomy of breast cancer. Oncogene (2011) 1.78
Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome. J Med Genet (2001) 1.70
Loss of heterozygosity and linkage analysis in breast carcinoma: indication for a putative third susceptibility gene on the short arm of chromosome 8. Oncogene (1995) 1.58
Analysis of the 10q23 chromosomal region and the PTEN gene in human sporadic breast carcinoma. Br J Cancer (1999) 1.54
Treatment with the mTOR inhibitor temsirolimus in patients with malignant PEComa. Ann Oncol (2010) 1.45
A critical analysis of treatment strategies in desmoid tumours: a review of a series of 106 cases. Eur J Surg Oncol (2008) 1.44
Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation. Genes Chromosomes Cancer (1998) 1.43
Timing of transabdominal chorionic villus sampling. Lancet (1990) 1.39
Mutations at BRCA1: the medullary breast carcinoma revisited. Cancer Res (1998) 1.39
FGFRI and PLAT genes and DNA amplification at 8p12 in breast and ovarian cancers. Genes Chromosomes Cancer (1993) 1.37
Gene expression profiling of human colon cancer cells following inhibition of signal transduction by 17-allylamino-17-demethoxygeldanamycin, an inhibitor of the hsp90 molecular chaperone. Oncogene (2000) 1.34
Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas. Cancer Res (1997) 1.33
Germ line mutation at BRCA1 affects the histoprognostic grade in hereditary breast cancer. Cancer Res (1996) 1.21
PTEN/MMAC1/TEP1 involvement in primary prostate cancers. Oncogene (1998) 1.20
Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas. Cancer Res (1997) 1.13
Mutational analysis of the PTEN gene in gliomas: molecular and pathological correlations. Int J Cancer (1999) 1.09
Loss of heterozygosity on chromosome arm 16q in breast cancer metastases. Genes Chromosomes Cancer (1997) 1.01
Frequencies of KIT and PDGFRA mutations in the MolecGIST prospective population-based study differ from those of advanced GISTs. Med Oncol (2011) 0.96
Prognosis and predictive value of KIT exon 11 deletion in GISTs. Br J Cancer (2009) 0.92
[Li-Fraumeni syndrome: update, new data and guidelines for clinical management]. Bull Cancer (2001) 0.92
Familial non-medullary thyroid carcinoma: pathology review in 27 affected cases from 13 French families. Clin Endocrinol (Oxf) (1999) 0.91
BRCA2 mutations in hereditary breast and ovarian cancer in France. Am J Hum Genet (1997) 0.91
Thyroid pathologic findings in patients with Cowden disease. Ann Diagn Pathol (1999) 0.90
Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions. Oncogene (1997) 0.90
MLH1 and MSH2 protein immunohistochemistry is useful for detection of hereditary non-polyposis colorectal cancer in young patients. Histopathology (2001) 0.89
Abnormal phenotype in a child with a "balanced" translocation 8/12 in mosaic state. Am J Med Genet (1987) 0.88
Role of thymus-eicosanoids in the immune response. Prostaglandins Leukot Essent Fatty Acids (1992) 0.87
High-resolution integrated map encompassing the breast cancer loss of heterozygosity region on human chromosome 16q22.1. Genomics (2000) 0.87
Identification of gene polymorphisms of human DNA topoisomerase I in the National Cancer Institute panel of human tumour cell lines. Br J Cancer (2006) 0.86
Contribution of PTEN large rearrangements in Cowden disease: a multiplex amplifiable probe hybridisation (MAPH) screening approach. J Med Genet (2008) 0.83
Marker segregation information in breast/ovarian cancer genetic counseling: is it still useful? Groupe Génétique et Cancer de la Fédération Nationale des Centres de Lutte Contre le Cancer. Am J Med Genet (1998) 0.77
[African human trypanosomiasis. Unusual discovery owing to recurrent acute pneumopathy]. Nouv Presse Med (1979) 0.77
No evidence for germline PTEN mutations in families with breast and brain tumours. Int J Cancer (1999) 0.77
[Thrombosis of the inferior vena cava with congenital deficiency of antithrombin III]. Nouv Presse Med (1980) 0.76
Feasibility of placental biopsy in the second trimester for fetal diagnosis. Am J Obstet Gynecol (1990) 0.75
Evolution of BCL-2/IgH hybrid gene RNA expression during treatment of T(14;18)-bearing follicular lymphomas. Br J Cancer (1999) 0.75
[Cutaneous and rectosigmoid cavernous hemangiomas. Bean's syndrome]. Sem Hop (1974) 0.75
[Improvement of a chromosomal technic for trophoblast biopsy. Apropos of 200 cases]. J Genet Hum (1988) 0.75
[Adrenal cortical adenoma and arterial hypertension. Adrenal vizualisation by scintillation with 131 I 19 iodo cholesterol (author's transl)]. Sem Hop (1981) 0.75
[Cowden's disease in an adolescent]. Ann Chir (2002) 0.75
[Chemodectomas. Their place in the A.P.U.D. system. Classification of neural crest diseases]. Rev Laryngol Otol Rhinol (Bord) (1981) 0.75
[Unusual genealogies in inflammatory cryptogenic colitis]. Rev Med Interne (1981) 0.75
Polymerase chain reaction diagnosis of t(14;18) from paraffin-embedded tissues fixed with Holland Bouin fluid. Diagn Mol Pathol (1998) 0.75
Myxoma of the mitral valve diagnosed by echocardiography. Am Heart J (1986) 0.75
[Collagenoses in otorhinolaryngology. Clinical, pathogenetic and therapeutic features]. Rev Laryngol Otol Rhinol (Bord) (1982) 0.75
[Total atrophy of the villi during primary agammaglobulinemia in adults. Therapeutic problems (author's transl)]. Ann Med Interne (Paris) (1979) 0.75
[Basal decidual hematoma persisting after biopsy of the trophoblast]. J Gynecol Obstet Biol Reprod (Paris) (1988) 0.75
Cowden's syndrome: possible association with testicular seminoma. Br J Dermatol (2004) 0.75
Risks of transabdominal chorionic villus sampling before the 12th week of amenorrhea. Prenat Diagn (1990) 0.75
[Macrocephaly and multiple hamartoma: a very variable entity]. Arch Pediatr (2004) 0.75
[Corticosensitive pseudoperiarteritis nodosa. Look for cholesterol embolism and aortic aneurysm]. Presse Med (1983) 0.75
[Placentocentesis, a new technic in the prenatal diagnosis of chromosome aberrations in the 3d trimester. A preliminary study apropos of 5 cases]. J Gynecol Obstet Biol Reprod (Paris) (1988) 0.75
[Is drepanocitic trait asymptomatic? (author's transl)]. Med Trop (Mars) (1979) 0.75
A study comparing transcervical with trans-abdominal chorionic villi sampling (CVS) Br J Obstet Gynaecol (1989) 0.75
[Myxoma of the mitral leaflet. Apropos of a case]. Arch Mal Coeur Vaiss (1985) 0.75
[Evaluation of the risks of transabdominal chorionic villus sampling. 600 cases]. J Gynecol Obstet Biol Reprod (Paris) (1991) 0.75
[Streptozotocin and malignant insulinomas. Apropos of the case. Review of the literature]. Sem Hop (1976) 0.75
De novo inv del(4) in an infant with the Wolf-Hirschhorn syndrome. Ann Genet (1987) 0.75
[Renal lesions in progressive systemic sclerosis. A report on five cases (author's transl)]. Sem Hop (1979) 0.75
[Multiple congenital arteriovenous fistulas. Case report concerning a late manifestation]. Rofo (1978) 0.75
Direct chromosome analysis in the second and third trimesters by placental biopsy in 30 pregnancies. Br J Obstet Gynaecol (1989) 0.75
[Hydatid cysts of the spleen. Current means of diagnosis]. Med Chir Dig (1974) 0.75
[Acute febrile muscle calcification of the biceps: microcrystalline myositis ossificans? (author's transl)]. Ann Radiol (Paris) (1981) 0.75
[Familial Mediterranean fever and fatty liver. effect of a long time colchicine treatment on triglyceride storage (author's transl)]. Ann Med Interne (Paris) (1981) 0.75
[Double trisomy and transmitted pericentric inversion (48,XXY, +21,inv(22)). Interchromosomal effect]. Ann Genet (1983) 0.75
[Cutaneous and rectosigmoidal cavernous hemangiomas. Bean's syndrome]. Lille Med (1976) 0.75
[Refractory anemia with partial myeloblastosis associated with bronchial cancer]. Nouv Presse Med (1978) 0.75
[Plasma cells leukaemia, cryoglobulins and antithrombin (author's transl)]. Sem Hop (1980) 0.75
[Partial trisomy of the proximal part of the long arm of chromosome 13]. Pediatrie (1982) 0.75
Allelic loss at chromosome 8p in human breast-cancer. Oncol Rep (1994) 0.75
Acute promyelocytic leukemia with (15;17) translocation and chromosome no. 11 deletion (q23). Leuk Res (1982) 0.75
[Sciatica due to chronic spontaneous lumbar epidural haematoma. Report of a case simulating a protruded disk syndrome (author's transl)]. Sem Hop (1981) 0.75
[Peripheral thrombophlebitis. "Paratuberculous syndrome" (author's transl)]. Sem Hop (1980) 0.75
Competitive polymerase chain reaction to quantify tumor cells in peripheral blood of patients with T(14;18)-bearing follicular non-Hodgkin's lymphoma: an exploratory study in 8 patients. Int J Cancer (1999) 0.75
[Bilharzial myelopathies (case report) (author's transl)]. Med Trop (Mars) (1980) 0.75
A simple method of chromosomal analysis for colonic adenomatous polyps. Cancer Genet Cytogenet (1989) 0.75
[Perisinusoidal fibrosis in idiopathic thrombopenic purpura]. Gastroenterol Clin Biol (1987) 0.75
[Portal hypertension in schistosomiasis (author's transl)]. Med Trop (Mars) (1980) 0.75
[Isotope scan using labelled cholesterol in the diagnosis of hypertension due to adrenal tumors (author's transl)]. Nouv Presse Med (1979) 0.75
[Extra-dural spinal hematoma and atypical lumbo-sciatica]. Nouv Presse Med (1980) 0.75
[Asystole caused by multiple rhizomelic congenital arteriovenous fistulas. Value of palliative surgery]. Nouv Presse Med (1980) 0.75
[A new case of Darier's atypical tuberculous ulcers]. Ann Dermatol Venereol (1986) 0.75
[Voluminous hypernephroma of intermittent development. Diagnostic difficulties (author's transl)]. J Radiol Electrol Med Nucl (1978) 0.75
[Glomerular nephropathy and schistosomiasis (author's transl)]. Med Trop (Mars) (1980) 0.75
Genetic alterations in colorectal cancer, comparative analysis of deletion events, and point mutations. Cancer Genet Cytogenet (1998) 0.75
Feto-placental discrepancy on direct chromosomal preparation from chorionic villus sampling of the second trimester. Clin Genet (1988) 0.75
[Value of skin immunofluorescence during B virus infections. Preliminary results]. Rev Med Interne (1980) 0.75
A simple method of chromosomal analysis for malignant solid tumors. Cancer Genet Cytogenet (1992) 0.75