| Year |
Citation |
Score |
| 2018 |
Cusin I, Teixeira D, Zahn-Zabal M, Rech de Laval V, Gleizes A, Viassolo V, Chappuis PO, Hutter P, Bairoch A, Gaudet P. A new bioinformatics tool to help assess the significance of BRCA1 variants. Human Genomics. 12: 36. PMID 29996917 DOI: 10.1186/S40246-018-0168-0 |
0.376 |
|
| 2015 |
Amin Al Olama A, Benlloch S, Antoniou AC, Giles GG, Severi G, Neal DE, Hamdy FC, Donovan JL, Muir K, Schleutker J, Henderson BE, Haiman CA, Schumacher FR, Pashayan N, Pharoah PD, ... ... Hutter P, et al. Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 24: 1121-9. PMID 25837820 DOI: 10.1158/1055-9965.Epi-14-0317 |
0.334 |
|
| 2015 |
Kovac MB, Kovacova M, Bachraty H, Bachrata K, Piscuoglio S, Hutter P, Ilencikova D, Bartosova Z, Tomlinson I, Roethlisberger B, Heinimann K. High-resolution breakpoint analysis provides evidence for the sequence-directed nature of genome rearrangements in hereditary disorders. Human Mutation. 36: 250-9. PMID 25418510 DOI: 10.1002/Humu.22734 |
0.344 |
|
| 2013 |
Rahner N, Steinke V, Schlegelberger B, Eisinger F, Hutter P, Olschwang S. Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012. European Journal of Human Genetics : Ejhg. 21. PMID 22892529 DOI: 10.1038/Ejhg.2012.164 |
0.333 |
|
| 2011 |
Kuiper RP, Vissers LE, Venkatachalam R, Bodmer D, Hoenselaar E, Goossens M, Haufe A, Kamping E, Niessen RC, Hogervorst FB, Gille JJ, Redeker B, Tops CM, van Gijn ME, van den Ouweland AM, ... ... Hutter P, et al. Recurrence and variability of germline EPCAM deletions in Lynch syndrome. Human Mutation. 32: 407-14. PMID 21309036 DOI: 10.1002/Humu.21446 |
0.437 |
|
| 2011 |
Kempers MJ, Kuiper RP, Ockeloen CW, Chappuis PO, Hutter P, Rahner N, Schackert HK, Steinke V, Holinski-Feder E, Morak M, Kloor M, Büttner R, Verwiel ET, van Krieken JH, Nagtegaal ID, et al. Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study. The Lancet. Oncology. 12: 49-55. PMID 21145788 DOI: 10.1016/S1470-2045(10)70265-5 |
0.474 |
|
| 2010 |
Rahner N, Steinke V, Schlegelberger B, Olschwang S, Eisinger F, Hutter P. Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2). European Journal of Human Genetics : Ejhg. 18. PMID 20104243 DOI: 10.1038/Ejhg.2009.232 |
0.467 |
|
| 2010 |
Bouzourene H, Hutter P, Losi L, Martin P, Benhattar J. Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutation. Familial Cancer. 9: 167-72. PMID 19949877 DOI: 10.1007/s10689-009-9302-4 |
0.377 |
|
| 2009 |
Olschwang S, Yu K, Lasset C, Baert-Desurmont S, Buisine MP, Wang Q, Hutter P, Rouleau E, Caron O, Bourdon V, Thomas G. Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers. Journal of Cancer Epidemiology. 2009: 791754. PMID 20445804 DOI: 10.1155/2009/791754 |
0.464 |
|
| 2009 |
Eeles RA, Kote-Jarai Z, Al Olama AA, Giles GG, Guy M, Severi G, Muir K, Hopper JL, Henderson BE, Haiman CA, Schleutker J, Hamdy FC, Neal DE, Donovan JL, Stanford JL, ... ... Hutter P, et al. Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. Nature Genetics. 41: 1116-21. PMID 19767753 DOI: 10.1038/Ng.450 |
0.35 |
|
| 2008 |
Kote-Jarai Z, Easton DF, Stanford JL, Ostrander EA, Schleutker J, Ingles SA, Schaid D, Thibodeau S, Dörk T, Neal D, Donovan J, Hamdy F, Cox A, Maier C, Vogel W, ... ... Hutter P, et al. Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 17: 2052-61. PMID 18708398 DOI: 10.1158/1055-9965.Epi-08-0317 |
0.339 |
|
| 2006 |
Soravia C, DeLozier CD, Dobbie Z, Berthod CR, Arrigoni E, Bründler MA, Blouin JL, Foulkes WD, Hutter P. Double frameshift mutations in APC and MSH2 in the same individual. International Journal of Colorectal Disease. 21: 79-83. PMID 16676398 DOI: 10.1007/s00384-005-0772-z |
0.419 |
|
| 2006 |
Li L, McVety S, Younan R, Liang P, Du Sart D, Gordon PH, Hutter P, Hogervorst FB, Chong G, Foulkes WD. Distinct patterns of germ-line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC). Human Mutation. 27: 388. PMID 16541406 DOI: 10.1002/Humu.9417 |
0.389 |
|
| 2006 |
Sieber OM, Segditsas S, Knudsen AL, Zhang J, Luz J, Rowan AJ, Spain SL, Thirlwell C, Howarth KM, Jaeger EE, Robinson J, Volikos E, Silver A, Kelly G, Aretz S, ... ... Hutter P, et al. Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutation. Gut. 55: 1440-8. PMID 16461775 DOI: 10.1136/Gut.2005.087106 |
0.494 |
|
| 2006 |
Russell AM, Zhang J, Luz J, Hutter P, Chappuis PO, Berthod CR, Maillet P, Mueller H, Heinimann K. Prevalence of MYH germline mutations in Swiss APC mutation-negative polyposis patients. International Journal of Cancer. Journal International Du Cancer. 118: 1937-40. PMID 16287072 DOI: 10.1002/Ijc.21470 |
0.499 |
|
| 2005 |
Mehenni H, Friedl W, Nelen MR, Hutter P, Brundler MA. An unexpected Cowden syndrome case found among members of a large familial adenomatous polyposis kindred. European Journal of Gastroenterology & Hepatology. 17: 1407-12. PMID 16292097 DOI: 10.1097/01.Meg.0000184983.38398.B6 |
0.503 |
|
| 2005 |
van der Klift H, Wijnen J, Wagner A, Verkuilen P, Tops C, Otway R, Kohonen-Corish M, Vasen H, Oliani C, Barana D, Moller P, Delozier-Blanchet C, Hutter P, Foulkes W, Lynch H, et al. Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC). Genes, Chromosomes & Cancer. 44: 123-38. PMID 15942939 DOI: 10.1002/Gcc.20219 |
0.424 |
|
| 2005 |
Soravia C, DeLozier CD, Dobbie Z, Berthod CR, Arrigoni E, Bründler MA, Blouin JL, Foulkes WD, Hutter P. Double frameshift mutations in APC and MSH2 in the same individual. International Journal of Colorectal Disease. 20: 466-470. PMID 15834612 DOI: 10.1007/S00384-005-0764-Z |
0.496 |
|
| 2005 |
Westphalen AA, Russell AM, Buser M, Berthod CR, Hutter P, Plasilova M, Mueller H, Heinimann K. Evidence for genetic anticipation in hereditary non-polyposis colorectal cancer. Human Genetics. 116: 461-5. PMID 15772852 DOI: 10.1007/S00439-005-1272-5 |
0.414 |
|
| 2004 |
Thiffault I, Foulkes WD, Marcus VA, Farber D, Kasprzak L, MacNamara E, Wong N, Hutter P, Radice P, Bertario L, Chong G. Putative common origin of two MLH1 mutations in Italian-Quebec hereditary non-polyposis colorectal cancer families. Clinical Genetics. 66: 137-43. PMID 15253764 DOI: 10.1111/J.1399-0004.2004.00274.X |
0.531 |
|
| 2003 |
Tapparel C, Reymond A, Girardet C, Guillou L, Lyle R, Lamon C, Hutter P, Antonarakis SE. The TPTE gene family: cellular expression, subcellular localization and alternative splicing. Gene. 323: 189-99. PMID 14659893 DOI: 10.1016/J.Gene.2003.09.038 |
0.361 |
|
| 2003 |
Soravia C, van der Klift H, Bründler MA, Blouin JL, Wijnen J, Hutter P, Fodde R, Delozier-Blanchet C. Prostate cancer is part of the hereditary non-polyposis colorectal cancer (HNPCC) tumor spectrum. American Journal of Medical Genetics. Part A. 121: 159-62. PMID 12910497 DOI: 10.1002/Ajmg.A.20106 |
0.376 |
|
| 2002 |
Paoloni-Giacobino A, Rey-Berthod C, Couturier A, Antonarakis SE, Hutter P. Differential rates of frameshift alterations in four repeat sequences of hereditary nonpolyposis colorectal cancer tumors. Human Genetics. 111: 284-9. PMID 12215842 DOI: 10.1007/S00439-002-0789-0 |
0.376 |
|
| 2002 |
Hutter P, Wijnen J, Rey-Berthod C, Thiffault I, Verkuijlen P, Farber D, Hamel N, Bapat B, Thibodeau SN, Burn J, Wu J, MacNamara E, Heinimann K, Chong G, Foulkes WD. An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1. Journal of Medical Genetics. 39: 323-7. PMID 12011148 DOI: 10.1136/Jmg.39.5.323 |
0.461 |
|
| 2001 |
Guipponi M, Tapparel C, Jousson O, Scamuffa N, Mas C, Rossier C, Hutter P, Meda P, Lyle R, Reymond A, Antonarakis SE. The murine orthologue of the Golgi-localized TPTE protein provides clues to the evolutionary history of the human TPTE gene family. Human Genetics. 109: 569-75. PMID 11810268 DOI: 10.1007/S004390100607 |
0.351 |
|
| 2001 |
Hutter P, Rey-Berthod C, Chappuis PO, Couturier A, Membrez V, Murphy A, Joris F, Schorderet DF, Delozier-Blanchet C, Soravia C. Molecular and clinical characteristics in 32 families affected with familial adenomatous polyposis. Human Mutation. 18: 550. PMID 11748858 DOI: 10.1002/Humu.1242 |
0.476 |
|
| 2001 |
Soravia C, Delozier-Blanchet C, Blouin JL, Bründler MA, Egger JF, Queneau PE, Roth AD, Marti MC, Antonarakis SE, Morel P, Hutter P. [Multidisciplinary management of hereditary colorectal cancer]. Swiss Surgery = Schweizer Chirurgie = Chirurgie Suisse = Chirurgia Svizzera. 7: 99-104. PMID 11407044 DOI: 10.1024/1023-9332.7.3.99 |
0.517 |
|
| 2000 |
Maillet P, Chappuis PO, Vaudan G, Dobbie Z, Müller H, Hutter P, Sappino AP. A polymorphism in the ATM gene modulates the penetrance of hereditary non-polyposis colorectal cancer. International Journal of Cancer. Journal International Du Cancer. 88: 928-31. PMID 11093816 DOI: 10.1002/1097-0215(20001215)88:6<928::Aid-Ijc14>3.0.Co;2-P |
0.535 |
|
| 2000 |
Hutter P, Couturier A, Rey-Berthod C. Two common forms of the human MLH1 gene may be associated with functional differences. Journal of Medical Genetics. 37: 776-81. PMID 11015456 DOI: 10.1136/Jmg.37.10.776 |
0.495 |
|
| 1999 |
Andreutti-Zaugg C, Couturier A, Chappuis P, Hutter P. Detection of protein truncating mutations in exons 1-14 of theAPC gene using an in vivo fusion protein assay Human Mutation. 13: 170-171. DOI: 10.1002/(Sici)1098-1004(1999)13:2<170::Aid-Humu13>3.0.Co;2-4 |
0.482 |
|
| 1998 |
Hutter P, Couturier A, Membrez V, Joris F, Sappino AP, Chappuis PO. Excess of hMLH1 germline mutations in Swiss families with hereditary non-polyposis colorectal cancer. International Journal of Cancer. Journal International Du Cancer. 78: 680-4. PMID 9833759 DOI: 10.1002/(Sici)1097-0215(19981209)78:6<680::Aid-Ijc3>3.0.Co;2-U |
0.545 |
|
| 1996 |
Hutter P, Couturier A, Scott RJ, Alday P, Delozier-Blanchet C, Cachat F, Antonarakis SE, Joris F, Gaudin M, D'Amato L, Buerstedde JM. Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation. Journal of Medical Genetics. 33: 636-40. PMID 8863153 DOI: 10.1136/Jmg.33.8.636 |
0.509 |
|
| 1996 |
Perrin G, Morris MA, Antonarakis SE, Boltshauser E, Hutter P. Two novel mutations affecting mRNA splicing of the neurofibromatosis type 1 (NF1) gene. Human Mutation. 7: 172-5. PMID 8829638 DOI: 10.1002/(Sici)1098-1004(1996)7:2<172::Aid-Humu15>3.0.Co;2-# |
0.412 |
|
| 1995 |
Antonarakis SE, Kazazian HH, Gitschier J, Hutter P, de Moerloose P, Morris MA. Molecular etiology of factor VIII deficiency in hemophilia A. Advances in Experimental Medicine and Biology. 386: 19-34. PMID 8851012 DOI: 10.1007/978-1-4613-0331-2_2 |
0.308 |
|
| 1994 |
Rossiter JP, Young M, Kimberland ML, Hutter P, Ketterling RP, Gitschier J, Horst J, Morris MA, Schaid DJ, de Moerloose P. Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells. Human Molecular Genetics. 3: 1035-9. PMID 7981669 DOI: 10.1093/Hmg/3.7.1035 |
0.373 |
|
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