M J Ligtenberg

Author PubWeight™ 24.00‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients. Nat Genet 1997 3.68
2 A multiplex PCR predictor for aCGH success of FFPE samples. Br J Cancer 2006 2.33
3 Cell membrane-associated mucins and their adhesion-modulating property. Trends Biochem Sci 1992 2.11
4 A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families. Am J Hum Genet 1997 2.01
5 Surveillance of women at high risk for hereditary ovarian cancer is inefficient. Br J Cancer 2006 1.45
6 Episialin (MUC1) inhibits cytotoxic lymphocyte-target cell interaction. J Immunol 1993 1.40
7 Control of antigenic variation in African trypanosomes. Cold Spring Harb Symp Quant Biol 1993 1.06
8 Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations. Biochem Biophys Res Commun 1994 1.05
9 The viral thymidine kinase gene as a tool for the study of mutagenesis in Trypanosoma brucei. Nucleic Acids Res 1996 0.96
10 A non-BRCA1/2 hereditary breast cancer sub-group defined by aCGH profiling of genetically related patients. Breast Cancer Res Treat 2011 0.93
11 Electronic reminders for pathologists promote recognition of patients at risk for Lynch syndrome: cluster-randomised controlled trial. Virchows Arch 2010 0.92
12 An alternative route for multistep tumorigenesis in a novel case of hereditary renal cell cancer and a t(2;3)(q35;q21) chromosome translocation. Am J Hum Genet 1998 0.89
13 Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation. Hum Genet 1995 0.88
14 Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15). Genes Chromosomes Cancer 2001 0.85
15 Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor gene. Hum Reprod 1998 0.81
16 The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region. Am J Hum Genet 1995 0.80
17 [From gene to disease; E-cadherin and hereditary diffuse gastric cancer]. Ned Tijdschr Geneeskd 2003 0.80
18 Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2. Br J Cancer 2011 0.79
19 Two intronic mutations in the adrenoleukodystrophy gene. Hum Mutat 1995 0.78
20 Testing for inherited susceptibility to breast and ovarian cancer. Eur J Obstet Gynecol Reprod Biol 1999 0.75
21 Detecting Lynch syndrome by pathologists. Verh Dtsch Ges Pathol 2007 0.75