| Year |
Citation |
Score |
| 2015 |
Blein S, Barjhoux L, Damiola F, Dondon MG, Eon-Marchais S, Marcou M, Caron O, Lortholary A, Buecher B, Vennin P, Berthet P, Noguès C, Lasset C, Gauthier-Villars M, ... ... Thomas G, et al. Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2. Plos One. 10: e0136192. PMID 26406445 DOI: 10.1371/Journal.Pone.0136192 |
0.313 |
|
| 2015 |
Blein S, Bardel C, Danjean V, McGuffog L, Healey S, Barrowdale D, Lee A, Dennis J, Kuchenbaecker KB, Soucy P, Terry MB, Chung WK, Goldgar DE, Buys SS, ... ... Thomas G, et al. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers. Breast Cancer Research : Bcr. 17: 61. PMID 25925750 DOI: 10.1186/S13058-015-0567-2 |
0.318 |
|
| 2012 |
Stephens PJ, Tarpey PS, Davies H, Van Loo P, Greenman C, Wedge DC, Nik-Zainal S, Martin S, Varela I, Bignell GR, Yates LR, Papaemmanuil E, Beare D, Butler A, Cheverton A, ... ... Thomas G, et al. The landscape of cancer genes and mutational processes in breast cancer. Nature. 486: 400-4. PMID 22722201 DOI: 10.1038/Nature11017 |
0.356 |
|
| 2012 |
Nik-Zainal S, Van Loo P, Wedge DC, Alexandrov LB, Greenman CD, Lau KW, Raine K, Jones D, Marshall J, Ramakrishna M, Shlien A, Cooke SL, Hinton J, Menzies A, Stebbings LA, ... ... Thomas G, et al. The life history of 21 breast cancers. Cell. 149: 994-1007. PMID 22608083 DOI: 10.1016/J.Cell.2012.04.023 |
0.35 |
|
| 2012 |
Jacobs KB, Yeager M, Zhou W, Wacholder S, Wang Z, Rodriguez-Santiago B, Hutchinson A, Deng X, Liu C, Horner MJ, Cullen M, Epstein CG, Burdett L, Dean MC, Chatterjee N, ... ... Thomas G, et al. Detectable clonal mosaicism and its relationship to aging and cancer. Nature Genetics. 44: 651-8. PMID 22561519 DOI: 10.1038/Ng.2270 |
0.355 |
|
| 2012 |
Postel-Vinay S, Véron AS, Tirode F, Pierron G, Reynaud S, Kovar H, Oberlin O, Lapouble E, Ballet S, Lucchesi C, Kontny U, González-Neira A, Picci P, Alonso J, Patino-Garcia A, ... ... Thomas G, et al. Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. Nature Genetics. 44: 323-7. PMID 22327514 DOI: 10.1038/Ng.1085 |
0.321 |
|
| 2012 |
Lee P, Fu YP, Figueroa JD, Prokunina-Olsson L, Gonzalez-Bosquet J, Kraft P, Wang Z, Jacobs KB, Yeager M, Horner MJ, Hankinson SE, Hutchinson A, Chatterjee N, Garcia-Closas M, Ziegler RG, ... ... Thomas G, et al. Fine mapping of 14q24.1 breast cancer susceptibility locus. Human Genetics. 131: 479-90. PMID 21959381 DOI: 10.1007/S00439-011-1088-4 |
0.324 |
|
| 2011 |
Ciampa J, Yeager M, Jacobs K, Thun MJ, Gapstur S, Albanes D, Virtamo J, Weinstein SJ, Giovannucci E, Willett WC, Cancel-Tassin G, Cussenot O, Valeri A, Hunter D, Hoover R, ... Thomas G, et al. Application of a novel score test for genetic association incorporating gene-gene interaction suggests functionality for prostate cancer susceptibility regions. Human Heredity. 72: 182-93. PMID 22086326 DOI: 10.1159/000331222 |
0.322 |
|
| 2010 |
Rodríguez-Santiago B, Malats N, Rothman N, Armengol L, Garcia-Closas M, Kogevinas M, Villa O, Hutchinson A, Earl J, Marenne G, Jacobs K, Rico D, Tardón A, Carrato A, Thomas G, et al. Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome. American Journal of Human Genetics. 87: 129-38. PMID 20598279 DOI: 10.1016/J.Ajhg.2010.06.002 |
0.371 |
|
| 2010 |
Rajaraman P, Brenner AV, Neta G, Pfeiffer R, Wang SS, Yeager M, Thomas G, Fine HA, Linet MS, Rothman N, Chanock SJ, Inskip PD. Risk of meningioma and common variation in genes related to innate immunity. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 19: 1356-61. PMID 20406964 DOI: 10.1158/1055-9965.Epi-09-1151 |
0.334 |
|
| 2009 |
Nan H, Kraft P, Qureshi AA, Guo Q, Chen C, Hankinson SE, Hu FB, Thomas G, Hoover RN, Chanock S, Hunter DJ, Han J. Genome-wide association study of tanning phenotype in a population of European ancestry. The Journal of Investigative Dermatology. 129: 2250-7. PMID 19340012 DOI: 10.1038/Jid.2009.62 |
0.304 |
|
| 2009 |
Shen M, Vermeulen R, Rajaraman P, Menashe I, He X, Chapman RS, Yeager M, Thomas G, Burdett L, Hutchinson A, Yuenger J, Chanock S, Lan Q. Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China. Environmental and Molecular Mutagenesis. 50: 285-90. PMID 19170196 DOI: 10.1002/Em.20452 |
0.304 |
|
| 2008 |
Mourra N, Zeitoun G, Portier G, Blanche H, Tubacher E, Gressin L, Flejou JF, Tiret E, Thomas G, Olschwang S. High-resolution genotyping of chromosome 8 in colon adenocarcinomas reveals recurrent break point but no gene mutation in the 8p21 region. Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 17: 90-3. PMID 18382363 DOI: 10.1097/PDM.0b013e31815bb5eb |
0.379 |
|
| 2008 |
Cook MB, Graubard BI, Quraishi SM, Yeager M, Chanock SJ, Crenshaw A, Erickson RL, Rubertone MV, Thomas G, McGlynn KA. Genetic variants in the 8q24 locus and risk of testicular germ cell tumors. Human Genetics. 123: 409-18. PMID 18373104 DOI: 10.1007/S00439-008-0491-Y |
0.326 |
|
| 2007 |
Demange L, Moncuit Cd, Thomas G, Olschwang S. Analyse phénotypique de 154 patients porteurs d’une mutation constitutionnelle du gène NF2 Revue Neurologique. 163: 1031-1038. PMID 18033041 DOI: 10.1016/S0035-3787(07)74175-9 |
0.321 |
|
| 2007 |
Brems H, Chmara M, Sahbatou M, Denayer E, Taniguchi K, Kato R, Somers R, Messiaen L, De Schepper S, Fryns JP, Cools J, Marynen P, Thomas G, Yoshimura A, Legius E. Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype. Nature Genetics. 39: 1120-6. PMID 17704776 DOI: 10.1038/Ng2113 |
0.349 |
|
| 2007 |
Schumacher FR, Feigelson HS, Cox DG, Haiman CA, Albanes D, Buring J, Calle EE, Chanock SJ, Colditz GA, Diver WR, Dunning AM, Freedman ML, Gaziano JM, Giovannucci E, Hankinson SE, ... ... Thomas G, et al. A common 8q24 variant in prostate and breast cancer from a large nested case-control study. Cancer Research. 67: 2951-6. PMID 17409400 DOI: 10.1158/0008-5472.Can-06-3591 |
0.311 |
|
| 2006 |
Bellanné-Chantelot C, Chaumarel I, Labopin M, Bellanger F, Barbu V, De Toma C, Delhommeau F, Casadevall N, Vainchenker W, Thomas G, Najman A. Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders. Blood. 108: 346-52. PMID 16537803 DOI: 10.1182/Blood-2005-12-4852 |
0.33 |
|
| 2006 |
Feigelson HS, Cox DG, Cann HM, Wacholder S, Kaaks R, Henderson BE, Albanes D, Altshuler D, Berglund G, Berrino F, Bingham S, Buring JE, Burtt NP, Calle EE, Chanock SJ, ... ... Thomas G, et al. Haplotype analysis of the HSD17B1 gene and risk of breast cancer: a comprehensive approach to multicenter analyses of prospective cohort studies. Cancer Research. 66: 2468-75. PMID 16489054 DOI: 10.1158/0008-5472.Can-05-3574 |
0.314 |
|
| 2006 |
Graakjaer J, Der-Sarkissian H, Schmitz A, Bayer J, Thomas G, Kolvraa S, Londoño-Vallejo JA. Allele-specific relative telomere lengths are inherited. Human Genetics. 119: 344-50. PMID 16440201 DOI: 10.1007/S00439-006-0137-X |
0.324 |
|
| 2006 |
Zeitoun G, Buecher B, Bayer J, Tanguy ML, Thomas G, Olschwang S. Retention of chromosome arm 5q in stage II colon cancers identifies 83% of liver metastasis occurrences Genes Chromosomes and Cancer. 45: 94-102. PMID 16206176 DOI: 10.1002/Gcc.20269 |
0.368 |
|
| 2006 |
Bellanne-Chantelot C, Labopin M, Bellanger F, Chaumarel I, Isnard F, Casadevall N, Vainchenker W, Thomas G, Najman A. Study of V617F JAK2-Positive and JAK2-Negative Patients within 18 Families with Myeloproliferative Disorders (MPD): Disease Characteristics and Evolution, EPOR and MPL Analysis. Blood. 108: 672-672. DOI: 10.1182/Blood.V108.11.672.672 |
0.309 |
|
| 2005 |
Hunter DJ, Riboli E, Haiman CA, Albanes D, Altshuler D, Chanock SJ, Haynes RB, Henderson BE, Kaaks R, Stram DO, Thomas G, Thun MJ, Blanché H, Buring JE, Burtt NP, et al. A candidate gene approach to searching for low-penetrance breast and prostate cancer genes. Nature Reviews. Cancer. 5: 977-85. PMID 16341085 DOI: 10.1038/Nrc1754 |
0.303 |
|
| 2005 |
Handra-Luca A, Condroyer C, de Moncuit C, Tepper M, Fléjou JF, Thomas G, Olschwang S. Vessels' morphology in SMAD4 and BMPR1A-related juvenile polyposis. American Journal of Medical Genetics. Part A. 138: 113-7. PMID 16152648 DOI: 10.1002/Ajmg.A.30897 |
0.339 |
|
| 2005 |
Bellanne-Chantelot C, Labopin M, Chaumarel I, Delhommeau F, Leroy G, Bellanger F, Thomas G, Vainchenker W, Najman A. Heterogeneous Distribution of the JAK2 Val617Phe Activating Mutation in Familial Myeloproliferative Disorders. Blood. 106: 115-115. DOI: 10.1182/Blood.V106.11.115.115 |
0.349 |
|
| 2004 |
Robanus-Maandag E, Giovannini M, Van Der Valk M, Niwa-Kawakita M, Abramowski V, Antonescu C, Thomas G, Berns A. Synergy of Nf2 and p53 mutations in development of malignant tumours of neural crest origin Oncogene. 23: 6541-6547. PMID 15221010 DOI: 10.1038/Sj.Onc.1207858 |
0.669 |
|
| 2004 |
Graakjaer J, Pascoe L, Der-Sarkissian H, Thomas G, Kolvraa S, Christensen K, Londoño-Vallejo J. The relative lengths of individual telomeres are defined in the zygote and strictly maintained during life. Aging Cell. 3: 97-102. PMID 15153177 DOI: 10.1111/J.1474-9728.2004.00093.X |
0.307 |
|
| 2003 |
Chamaillard M, Philpott D, Girardin SE, Zouali H, Lesage S, Chareyre F, Bui TH, Giovannini M, Zaehringer U, Penard-Lacronique V, Sansonetti PJ, Hugot JP, Thomas G. Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases. Proceedings of the National Academy of Sciences of the United States of America. 100: 3455-60. PMID 12626759 DOI: 10.1073/Pnas.0530276100 |
0.492 |
|
| 2003 |
Parc Y, Boisson C, Thomas G, Olschwang S. Cancer risk in 348 French MSH2 or MLH1 gene carriers Journal of Medical Genetics. 40: 208-213. PMID 12624141 DOI: 10.1136/Jmg.40.3.208 |
0.373 |
|
| 2003 |
Der-Sarkissian H, Vergnaud G, Borde YM, Thomas G, Londoño-Vallejo JA. Segmental polymorphisms in the proterminal regions of a subset of human chromosomes. Genome Research. 12: 1673-8. PMID 12421753 DOI: 10.1101/Gr.322802 |
0.391 |
|
| 2002 |
Busson-Le Coniat M, Boucher N, Blanché H, Thomas G, Berger R. Chromosome studies of in vitro senescent lymphocytes: nonrandom trisomy 2. Annales De GéNÉTique. 45: 193-6. PMID 12668167 DOI: 10.1016/S0003-3995(02)01138-3 |
0.315 |
|
| 2002 |
Rebischung C, Gérard J, Gayet J, Thomas G, Hamelin R, Laurent-Puig P. Prognostic value of P53 mutations in rectal carcinoma International Journal of Cancer. 100: 131-135. PMID 12115559 DOI: 10.1002/Ijc.10480 |
0.324 |
|
| 2002 |
Kalamarides M, Niwa-Kawakita M, Leblois H, Abramowski V, Perricaudet M, Janin A, Thomas G, Gutmann DH, Giovannini M. Nf2 gene inactivation in arachnoidal cells is rate-limiting for meningioma development in the mouse. Genes & Development. 16: 1060-5. PMID 12000789 DOI: 10.1101/Gad.226302 |
0.602 |
|
| 2002 |
Lesage S, Zouali H, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, O'Morain C, Gassull M, Binder V, Finkel Y, Modigliani R, Gower-Rousseau C, Macry J, Merlin F, ... ... Thomas G, et al. CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease. American Journal of Human Genetics. 70: 845-57. PMID 11875755 DOI: 10.1086/339432 |
0.341 |
|
| 2002 |
Zouali H, Chamaillard M, Lesage S, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, Montague S, Gassull M, Christensen S, Finkel Y, Gower-Rousseau C, Modigliani R, Macry J, ... ... Thomas G, et al. Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease. European Journal of Human Genetics : Ejhg. 9: 731-42. PMID 11781683 DOI: 10.1038/Sj.Ejhg.5200710 |
0.392 |
|
| 2001 |
Goutebroze L, Sarkissian HD, Brault E, Thomas G. Assignment of the Schwannomin-interacting Protein 1 (SCHIP1) gene to human chromosome band 3q25 by in situ hybridization and with somatic cell hybrids Cytogenetic and Genome Research. 94: 96-97. PMID 11701967 DOI: 10.1159/000048795 |
0.381 |
|
| 2001 |
Miceli-Richard C, Lesage S, Rybojad M, Prieur AM, Manouvrier-Hanu S, Häfner R, Chamaillard M, Zouali H, Thomas G, Hugot JP. CARD15 mutations in Blau syndrome. Nature Genetics. 29: 19-20. PMID 11528384 DOI: 10.1038/Ng720 |
0.308 |
|
| 2001 |
Londoño-Vallejo JA, DerSarkissian H, Cazes L, Thomas G. Differences in telomere length between homologous chromosomes in humans Nucleic Acids Research. 29: 3164-3171. PMID 11470873 DOI: 10.1093/Nar/29.15.3164 |
0.362 |
|
| 2001 |
Hugot JP, Chamaillard M, Zouali H, Lesage S, Cézard JP, Belaiche J, Almer S, Tysk C, O'morain CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent-Puig P, ... ... Thomas G, et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease Nature. 411: 599-603. PMID 11385576 DOI: 10.1038/35079107 |
0.332 |
|
| 2001 |
Laurent–Puig P, Legoix P, Bluteau O, Belghiti J, Franco D, Binot F, Monges G, Thomas G, Bioulac–Sage P, Zucman–Rossi J. Genetic alterations associated with hepatocellular carcinomas define distinct pathways of hepatocarcinogenesis. Gastroenterology. 120: 1763-1773. PMID 11375957 DOI: 10.1053/Gast.2001.24798 |
0.424 |
|
| 2000 |
Nemani M, Sahbatou M, Blanché H, Thomas G, Pascoe L. The efficiency of genetic analysis of DNA from aged siblings to detect chromosomal regions implicated in longevity. Mechanisms of Ageing and Development. 119: 25-39. PMID 11040399 DOI: 10.1016/S0047-6374(00)00165-2 |
0.34 |
|
| 2000 |
Medhioub M, Vaury C, Hamelin R, Thomas G. Lack of somatic mutation in the coding sequence of SIAH1 in tumors hemizygous for this candidate tumor suppressor gene. International Journal of Cancer. 87: 794-7. PMID 10956387 DOI: 10.1002/1097-0215(20000915)87:6<794::Aid-Ijc5>3.0.Co;2-B |
0.439 |
|
| 2000 |
Legoix P, Sarkissian HD, Cazes L, Giraud S, Sor F, Rouleau GA, Lenoir G, Thomas G, Zucman-Rossi J. Molecular characterization of germline NF2 gene rearrangements. Genomics. 65: 62-6. PMID 10777666 DOI: 10.1006/Geno.2000.6139 |
0.454 |
|
| 2000 |
López-Correa C, Zucman-Rossi J, Brems H, Thomas G, Legius E. NF2 gene deletion in a family with a mild phenotype. Journal of Medical Genetics. 37: 75-77. PMID 10691417 DOI: 10.1136/Jmg.37.1.75 |
0.414 |
|
| 2000 |
Niwa-Kawakita M, Abramowski V, Kalamarides M, Thomas G, Giovannini M. Targeted expression of Cre recombinase to myelinating cells of the central nervous system in transgenic mice Genesis. 26: 127-129. PMID 10686606 DOI: 10.1002/(Sici)1526-968X(200002)26:2<127::Aid-Gene8>3.0.Co;2-H |
0.52 |
|
| 2000 |
Goutebroze L, Brault E, Muchardt C, Camonis J, Thomas G. Cloning and characterization of SCHIP-1, a novel protein interacting specifically with spliced isoforms and naturally occurring mutant NF2 proteins. Molecular and Cellular Biology. 20: 1699-712. PMID 10669747 DOI: 10.1128/Mcb.20.5.1699-1712.2000 |
0.346 |
|
| 2000 |
Duval A, Iacopetta B, Ranzani GN, Lothe RA, Thomas G, Hamelin R. Variable mutation frequencies in coding repeats of TCF-4 and other target genes in colon, gastric and endometrial carcinoma showing microsatellite instability. Oncogene. 18: 6806-9. PMID 10597289 DOI: 10.1038/Sj.Onc.1203287 |
0.382 |
|
| 2000 |
Giovannini M, Robanus-Maandag E, Valk Mvd, Niwa-Kawakita M, Abramowski V, Goutebroze L, Woodruff JM, Berns A, Thomas G. Conditional biallelic Nf2 mutation in the mouse promotes manifestations of human neurofibromatosis type 2 Genes & Development. 14: 1617-1630. DOI: 10.1101/Gad.14.13.1617 |
0.587 |
|
| 1999 |
Zhou XP, Sanson M, Hoang-Xuan K, Robin E, Taillandier L, He J, Mokhtari K, Cornu P, Delattre JY, Thomas G, Hamelin R. Germline mutations of p53 but not p16/CDKN2 or PTEN/MMAC1 tumor suppressor genes predispose to gliomas. The ANOCEF Group. Association des NeuroOncologues d'Expression Française. Annals of Neurology. 46: 913-6. PMID 10589545 DOI: 10.1002/1531-8249(199912)46:6<913::Aid-Ana15>3.0.Co;2-X |
0.39 |
|
| 1999 |
Kovar H, Jugovic D, Melot T, Zoubek A, Lenoir G, Fink F, Philip I, Turc-Carel C, Thomas G, Zucman-Rossi J. Cryptic exons as a source of increased diversity of Ewing tumor-associated EWS-FLI1 chimeric products. Genomics. 60: 371-374. PMID 10493837 DOI: 10.1006/Geno.1999.5919 |
0.345 |
|
| 1999 |
Lerebours F, Olschwang S, Thuille B, Schmitz A, Fouchet P, Buecher B, Martinet N, Galateau F, Thomas G. Fine deletion mapping of chromosome 8p in non-small-cell lung carcinoma. International Journal of Cancer. 81: 854-8. PMID 10362129 DOI: 10.1002/(Sici)1097-0215(19990611)81:6<854::Aid-Ijc3>3.0.Co;2-1 |
0.463 |
|
| 1999 |
Lerebours F, Olschwang S, Thuille B, Schmitz A, Fouchet P, Laurent-Puig P, Boman F, Fléjou JF, Monges G, Paraf F, Bedossa P, Sabourin JC, Salmon RJ, Parc R, Thomas G. Deletion mapping of the tumor suppressor locus involved in colorectal cancer on chromosome band 8p21. Genes, Chromosomes & Cancer. 25: 147-53. PMID 10337998 DOI: 10.1002/(Sici)1098-2264(199906)25:2<147::Aid-Gcc10>3.0.Co;2-Z |
0.47 |
|
| 1999 |
Legoix P, Legrand M, Ollagnon E, Lenoir G, Thomas G, Zucman-Rossi J. Characterisation of 16 polymorphic markers in the NF2 gene: application to hemizygosity detection. Human Mutation. 13: 290-293. PMID 10220142 DOI: 10.1002/(Sici)1098-1004(1999)13:4<290::Aid-Humu5>3.0.Co;2-C |
0.426 |
|
| 1999 |
Giovannini M, Robanus-Maandag E, Niwa-Kawakita M, van der Valk M, Woodruff JM, Goutebroze L, Mérel P, Berns A, Thomas G. Schwann cell hyperplasia and tumors in transgenic mice expressing a naturally occurring mutant NF2 protein. Genes & Development. 13: 978-86. PMID 10215625 DOI: 10.1101/Gad.13.8.978 |
0.59 |
|
| 1999 |
Zhou X, Li Y, Hoang‐Xuan K, Laurent‐Puig P, Mokhtari K, Longy M, Sanson M, Delattre J, Thomas G, Hamelin R. Mutational analysis of the PTEN gene in gliomas: molecular and pathological correlations. International Journal of Cancer. 84: 150-154. PMID 10096247 DOI: 10.1002/(SICI)1097-0215(19990420)84:2<150::AID-IJC10>3.0.CO;2-# |
0.439 |
|
| 1999 |
Li YJ, Hoang-Xuan K, Zhou XP, Sanson M, Mokhtari K, Faillot T, Cornu P, Poisson M, Thomas G, Hamelin R. Analysis of the p21 gene in gliomas. Journal of Neuro-Oncology. 40: 107-11. PMID 9892092 DOI: 10.1023/A:1006149021810 |
0.398 |
|
| 1998 |
Olschwang S, Richard S, Boisson C, Giraud S, Laurent-Puig P, Resche F, Thomas G. Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma Human Mutation. 12: 424-430. PMID 9829912 DOI: 10.1002/(Sici)1098-1004(1998)12:6<424::Aid-Humu9>3.0.Co;2-H |
0.371 |
|
| 1998 |
Zucman-Rossi J, Legoix P, Sarkissian HD, Cheret G, Sor F, Bernardi A, Cazes L, Giraud S, Ollagnon E, Lenoir G, Thomas G. NF2 Gene in Neurofibromatosis Type 2 Patients Human Molecular Genetics. 7: 2095-2101. PMID 9817927 DOI: 10.1093/Hmg/7.13.2095 |
0.401 |
|
| 1998 |
Zucman-Rossi J, Legoix P, Victor J, Lopez B, Thomas G. Chromosome translocation based on illegitimate recombination in human tumors Proceedings of the National Academy of Sciences of the United States of America. 95: 11786-11791. PMID 9751743 DOI: 10.1073/Pnas.95.20.11786 |
0.406 |
|
| 1998 |
Deguen B, Goutebroze L, Giovannini M, Boisson C, Neut Rvd, Jaurand M, Thomas G. Heterogeneity of mesothelioma cell lines as defined by altered genomic structure and expression of the NF2 gene. International Journal of Cancer. 77: 554-560. PMID 9679758 DOI: 10.1002/(Sici)1097-0215(19980812)77:4<554::Aid-Ijc14>3.0.Co;2-6 |
0.599 |
|
| 1998 |
Olschwang S, Slezak P, Roze M, Jaramillo E, Nakano H, Koizumi K, Rubio CA, Laurent-Puig P, Thomas G. Somatically Acquired Genetic Alterations In Flat Colorectal Neoplasias International Journal of Cancer. 77: 366-369. PMID 9663597 DOI: 10.1002/(Sici)1097-0215(19980729)77:3<366::Aid-Ijc10>3.0.Co;2-6 |
0.392 |
|
| 1998 |
Zhou X, Hoang J, Li Y, Seruca R, Carneiro F, Sobrinho-Simoes M, Lothe RA, Gleeson CM, Russell SEH, Muzeau F, Fléjou J, Hoang-Xuan K, Lidereau R, Thomas G, Hamelin R. Determination of the replication error phenotype in human tumors without the requirement for matching normal DNA by analysis of mononucleotide repeat microsatellites Genes, Chromosomes and Cancer. 21: 101-107. PMID 9491320 DOI: 10.1002/(Sici)1098-2264(199802)21:2<101::Aid-Gcc4>3.0.Co;2-4 |
0.355 |
|
| 1997 |
Zhou XP, Hoang JM, Cottu P, Thomas G, Hamelin R. Allelic profiles of mononucleotide repeat microsatellites in control individuals and in colorectal tumors with and without replication errors Oncogene. 15: 1713-1718. PMID 9349505 DOI: 10.1038/Sj.Onc.1201337 |
0.349 |
|
| 1997 |
Olschwang S, Hamelin R, Laurent-Puig P, Thuille B, De Rycke Y, Li YJ, Muzeau F, Girodet J, Salmon RJ, Thomas G. Alternative genetic pathways in colorectal carcinogenesis. Proceedings of the National Academy of Sciences of the United States of America. 94: 12122-7. PMID 9342373 DOI: 10.1073/Pnas.94.22.12122 |
0.406 |
|
| 1997 |
Desmaze C, Brizard F, Turc-Carel C, Melot T, Delattre O, Thomas G, Aurias A. Multiple chromosomal mechanisms generate an EWS/FLI1 or an EWS/ERG fusion gene in Ewing tumors☆ Cancer Genetics and Cytogenetics. 97: 12-19. PMID 9242212 DOI: 10.1016/S0165-4608(96)00326-3 |
0.428 |
|
| 1997 |
Kehrer-Sawatzki H, Udart M, Krone W, Baden R, Fahsold R, Thomas G, Schmucker B, Assum G. Mutational analysis and expression studies of the neurofibromatosis type 2 (NF2) gene in a patient with a ring chromosome 22 and NF2. Human Genetics. 100: 67-74. PMID 9225971 DOI: 10.1007/S004390050467 |
0.432 |
|
| 1997 |
Muzeau F, Fléjou JF, Thomas G, Hamelin R. Loss of heterozygosity on chromosome 9 and p16 (MTS1, CDKN2) gene mutations in esophageal cancers International Journal of Cancer. 72: 27-30. PMID 9212218 DOI: 10.1002/(Sici)1097-0215(19970703)72:1<27::Aid-Ijc3>3.0.Co;2-6 |
0.469 |
|
| 1997 |
Peter M, Couturier J, Pacquement H, Michon J, Thomas G, Magdelenat H, Delattre O. A new member of the ETS family fused to EWS in Ewing tumors Oncogene. 14: 1159-1164. PMID 9121764 DOI: 10.1038/Sj.Onc.1200933 |
0.366 |
|
| 1997 |
Zucman-Rossi J, Batzer MA, Stoneking M, Delattre O, Thomas G. Interethnic polymorphism of EWS intron 6: Genome plasticity mediated by Alu retroposition and recombination Human Genetics. 99: 357-363. PMID 9050923 DOI: 10.1007/S004390050372 |
0.33 |
|
| 1996 |
Zucman-Rossi J, Legoix P, Thomas G. Identification of new members of the Gas2 and Ras families in the 22q12 chromosome region. Genomics. 38: 247-254. PMID 8975699 DOI: 10.1006/Geno.1996.0625 |
0.452 |
|
| 1996 |
Tomlinson IP, Olschwang S, Abelovitch D, Nakamura Y, Bodmer WF, Thomas G, Markie D. Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' disease. Annals of Human Genetics. 60: 377-84. PMID 8912790 DOI: 10.1111/J.1469-1809.1996.Tb00435.X |
0.401 |
|
| 1996 |
Demczuk S, Thomas G, Aurias A. Isolation of a Novel Gene from the DiGeorge Syndrome Critical Region with Homology to Drosophila gdl and to Human LAMC1 Genes Human Molecular Genetics. 5: 633-638. PMID 8733130 DOI: 10.1093/Hmg/5.5.633 |
0.378 |
|
| 1996 |
Peter M, Mugneret F, Aurias A, Thomas G, Magdelenat H, Delattre O. An EWS/ERG fusion with a truncated N-terminal domain of EWS in a Ewing's tumor International Journal of Cancer. 67: 339-342. PMID 8707406 DOI: 10.1002/(Sici)1097-0215(19960729)67:3<339::Aid-Ijc6>3.0.Co;2-S |
0.393 |
|
| 1996 |
Doz F, Peter M, Schleiermacher G, Vielh P, Validire P, Putterman M, Blanquet V, Desjardins L, Dufier J-, Zucker J-, Mosseri V, Thomas G, Magdelénat H, Delattre O. N-MYC amplification, loss of heterozygosity on the short arm of chromosome 1 and DNA ploidy in retinoblastoma European Journal of Cancer. 32: 645-649. PMID 8695269 DOI: 10.1016/0959-8049(95)00626-5 |
0.42 |
|
| 1996 |
Schleiermacher G, Delattre O, Peter M, Mosseri V, Delonlay P, Vielh P, Thomas G, Zucker J, Magdelénat H, Michon J. Clinical relevance of loss of heterozygosity of the short arm of chromosome 1 in neuroblastoma : A single-institution study International Journal of Cancer. 69: 73-78. PMID 8608986 DOI: 10.1002/(Sici)1097-0215(19960422)69:2<73::Aid-Ijc1>3.0.Co;2-S |
0.327 |
|
| 1996 |
Hugot JP, Laurent-Puig P, Gower-Rousseau C, Olson JM, Lee JC, Beaugerie L, Naom I, Dupas JL, Van Gossum A, Orholm M, Bonaiti-Pellie C, Weissenbach J, Mathew CG, Lennard-Jones JE, Cortot A, ... ... Thomas G, et al. Mapping of a susceptibility locus for Crohn's disease on chromosome 16. Nature. 379: 821-3. PMID 8587604 DOI: 10.1038/379821A0 |
0.35 |
|
| 1996 |
Thomas G, Merel P, Giovannini M, Niwa-Kawakita M, Robanus-Maandag E, Berns A, Goutebrose L, Deguen B. The NF2 tumor suppressor gene Cancer Genetics and Cytogenetics. 91: 110. DOI: 10.1016/S0165-4608(97)82511-3 |
0.57 |
|
| 1995 |
Hulsebos TJ, Gilbert DJ, Delattre O, Smink LJ, Dunham I, Westerveld A, Thomas G, Jenkins NA, Copeland NG. Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5. Genomics. 29: 712-8. PMID 8575764 DOI: 10.1006/Geno.1995.9947 |
0.346 |
|
| 1995 |
Hoang-Xuan K, Merel P, Vega F, Hugot JP, Cornu P, Delattre JY, Poisson M, Thomas G, Delattre O. Analysis of the NF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas. International Journal of Cancer. 60: 478-81. PMID 7829260 DOI: 10.1002/Ijc.2910600409 |
0.48 |
|
| 1995 |
Anglard P, Melot T, Guérin E, Thomas G, Basset P. Structure and Promoter Characterization of the Human Stromelysin-3 Gene Journal of Biological Chemistry. 270: 20337-20344. PMID 7657606 DOI: 10.1074/Jbc.270.35.20337 |
0.334 |
|
| 1995 |
Demczuk S, Aledo R, Zucman J, Delattre O, Desmaze C, Dauphinot L, Jalbert P, Rouleau GA, Thomas G, Aurias A. Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity. Human Molecular Genetics. 4: 551-8. PMID 7633403 DOI: 10.1093/Hmg/4.4.551 |
0.335 |
|
| 1995 |
Demczuk S, Lévy A, Aubry M, Croquette MF, Philip N, Prieur M, Sauer U, Bouvagnet P, Rouleau GA, Thomas G. Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature. Human Genetics. 96: 9-13. PMID 7607662 DOI: 10.1007/Bf00214179 |
0.358 |
|
| 1995 |
Bijlsma EK, Merel P, Fleury P, van Asperen CJ, Westerveld A, Delattre O, Thomas G, Hulsebos TJ. Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 gene. Human Genetics. 96: 1-5. PMID 7607639 DOI: 10.1007/Bf00214177 |
0.361 |
|
| 1995 |
Olschwang S, Laurent‐Puig P, Melot T, Thuille B, Thomas G. High resolution genetic map of the adenomatous polyposis coli gene (APC) region American Journal of Medical Genetics. 56: 413-419. PMID 7604852 DOI: 10.1002/Ajmg.1320560413 |
0.395 |
|
| 1995 |
Schleiermacher G, Peter M, Michon J, Zucker J-, Thomas G, Magdelénat H, Delattre O. A multiplex PCR assay for routine evaluation of deletion of the short arm of chromosome 1 in neuroblastoma. European Journal of Cancer. 31: 535-538. PMID 7576961 DOI: 10.1016/0959-8049(95)00008-7 |
0.412 |
|
| 1995 |
Olschwang S, Boisson C, Richard S, Resche F, Thomas G. DNA-based presymptomatic diagnosis for the von Hippel-Lindau disease by linkage analysis. European Journal of Human Genetics. 3: 108-115. PMID 7552140 DOI: 10.1159/000472284 |
0.332 |
|
| 1995 |
Bijlsma EK, Voesten AM, Bijleveld EH, Troost D, Westerveld A, Mérel P, Thomas G, Hulsebos TJ. Molecular analysis of genetic changes in ependymomas. Genes, Chromosomes & Cancer. 13: 272-7. PMID 7547635 DOI: 10.1002/Gcc.2870130407 |
0.439 |
|
| 1995 |
Thomas G. 1016 Involvement of NF2 gene alterations in tumorigenesis European Journal of Cancer. 31. DOI: 10.1016/0959-8049(95)96264-E |
0.455 |
|
| 1995 |
Delattre O, Peter M, Fagnoux C, Thomas G, Magdelenat H. 601 Molecular diagnosis of Ewing's tumours European Journal of Cancer. 31: S127. DOI: 10.1016/0959-8049(95)95855-Z |
0.328 |
|
| 1994 |
Hamelin R, Laurent-Puig P, Olschwang S, Jego N, Asselain B, Remvikos Y, Girodet J, Salmon RJ, Thomas G. Association of p53 mutations with short survival in colorectal cancer Gastroenterology. 106: 42-48. PMID 8276207 DOI: 10.1016/S0016-5085(94)94217-X |
0.398 |
|
| 1994 |
Olschwang S, Tiret A, Laurent-Puig P, Muleris M, Parc R, Thomas G. Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients. Cell. 75: 959-68. PMID 8252631 DOI: 10.1016/0092-8674(93)90539-3 |
0.361 |
|
| 1994 |
Desmaze C, Zucman J, Delattre O, Melot T, Thomas G, Aurias A. Interphase molecular cytogenetics of Ewing's sarcoma and peripheral neuroepithelioma t(11;22) with flanking and overlapping cosmid probes Cancer Genetics and Cytogenetics. 74: 13-18. PMID 8194041 DOI: 10.1016/0165-4608(94)90022-1 |
0.372 |
|
| 1994 |
Ruttledge MH, Xie Y, Han F, Giovannini M, Janson M, Fransson I, Werelius B, Delattre O, Thomas G, Evans G, Dumanski JP. Physical mapping of the NF2/meningioma region on human chromosome 22q12. Genomics. 19: 52-59. PMID 8188242 DOI: 10.1006/Geno.1994.1012 |
0.716 |
|
| 1994 |
Twist EC, Ruttledge MH, Rousseau M, Sanson M, Papi L, Merel P, Delattre O, Thomas G, Rouleau GA. The neurofibromatosis type 2 gene is inactivated in schwannomas. Human Molecular Genetics. 3: 147-51. PMID 8162016 DOI: 10.1093/Hmg/3.1.147 |
0.437 |
|
| 1994 |
Hamelin R, Barichard F, Henry I, Junien C, Thomas G. Single base pair germ-line deletion in the p53 gene in a cancer predisposed family. Human Genetics. 94: 88-90. PMID 8034301 DOI: 10.1007/Bf02272849 |
0.393 |
|
| 1994 |
Moreau-Aubry A, Andre MT, Devilder MC, Resche F, Delattre O, Thomas G, Moisan JP. Characterization of several DNA polymorphic markers in the LIF gene region. Human Genetics. 94: 450-1. PMID 7927349 DOI: 10.1007/Bf00201613 |
0.397 |
|
| 1994 |
Kurahashi H, Akagi K, Yana I, Melot T, Delattre O, Thomas G, Okada S, Takai Si, Nishisho I. Refined mapping of eight cosmid markers on human chromosome 22 Journal of Human Genetics. 39: 243-248. PMID 7916219 DOI: 10.1007/Bf01876844 |
0.407 |
|
| 1994 |
Thomas G. Advances in the genetics and molecular biology of colorectal tumors Current Opinion in Oncology. 6: 406-412. PMID 7803543 DOI: 10.1097/00001622-199407000-00014 |
0.425 |
|
| 1994 |
Hugot JP, Laurent-Puig P, Gower-Rousseau C, Caillat-Zucman S, Beaugerie L, Dupas J, Gossum AV, Bonaïti-Pellie C, Cortot A, Thomas G. Linkage analyses of chromosome 6 loci, including HLA, in familial aggregations of Crohn disease American Journal of Medical Genetics. 52: 207-213. PMID 7802010 DOI: 10.1002/Ajmg.1320520216 |
0.39 |
|
| 1994 |
Thomas G, Delattre O, Zucman J, Merel P, Desmaze C, Melot T, Sanson M, Hoang-Xuan K, Plougastel B, Dejong P. Genetic alterations in the chromosome 22q12 region associated with development of neuroectodermal tumors. Cold Spring Harbor Symposia On Quantitative Biology. 59: 555-64. PMID 7587112 DOI: 10.1101/Sqb.1994.059.01.062 |
0.401 |
|
| 1994 |
Bijlsma EK, Merel P, Bosch DA, Westerveld A, Delattre O, Thomas G, Hulsebos TJ. Analysis of mutations in the SCH gene in schwannomas. Genes, Chromosomes & Cancer. 11: 7-14. PMID 7529050 DOI: 10.1002/Gcc.2870110103 |
0.432 |
|
| 1994 |
Hamelin R, Fléjou J, Muzeau F, Potet F, Laurent-Puig P, Fékété F, Thomas G. TP53 gene mutations and p53 protein immunoreactivity in malignant and premalignant Barrett's esophagus Gastroenterology. 107: 1012-1018. PMID 7523212 DOI: 10.1016/0016-5085(94)90225-9 |
0.358 |
|
| 1994 |
Schleiermacher G, Peter M, Michon J, Hugot J, Vielh P, Zucker J, Magdelénat H, Thomas G, Delattre O. Two distinct deleted regions on the short arm of chromosome I in neuroblastoma Genes, Chromosomes and Cancer. 10: 275-281. PMID 7522542 DOI: 10.1002/Gcc.2870100409 |
0.471 |
|
| 1994 |
Thomas G, Delattre O, Zucman J, Merel P, Dejong P, Rouleau G, Aurias A. Oncogene and antioncogene from the 22q12 region involved in neuroectodermal tumours Cancer Genetics and Cytogenetics. 77: 156. DOI: 10.1016/0165-4608(94)90263-1 |
0.312 |
|
| 1993 |
Lamour V, Lévy N, Desmaze C, Baude V, Lécluse Y, Delattre O, Bernheim A, Thomas G, Aurias A, Lipinski M. Isolation of cosmids and fetal brain cDNAs from the proximal long arm of human chromosome 22. Human Molecular Genetics. 2: 535-40. PMID 8518791 DOI: 10.1093/Hmg/2.5.535 |
0.411 |
|
| 1993 |
May WA, Gishizky ML, Lessnick SL, Lunsford LB, Lewis BC, Delattre O, Zucman J, Thomas G, Denny CT. Ewing sarcoma 11;22 translocation produces a chimeric transcription factor that requires the DNA-binding domain encoded by FLI1 for transformation. Proceedings of the National Academy of Sciences of the United States of America. 90: 5752-6. PMID 8516324 DOI: 10.1073/Pnas.90.12.5752 |
0.368 |
|
| 1993 |
Marineau C, Baron C, Delattre O, Zucman J, Thomas G, Rouleau GA. Dinucleotide repeat polymorphism at the D22S268 locus. Human Molecular Genetics. 2: 336. PMID 8499931 DOI: 10.1093/Hmg/2.3.336-A |
0.313 |
|
| 1993 |
Rose TM, Lagrou MJ, Fransson I, Werelius B, Delattre O, Thomas G, de Jong PJ, Todaro GJ, Dumanski JP. The genes for oncostatin M (OSM) and leukemia inhibitory factor (LIF) are tightly linked on human chromosome 22. Genomics. 17: 136-40. PMID 8406444 DOI: 10.1006/Geno.1993.1294 |
0.417 |
|
| 1993 |
Muleris M, Laurent-Puig P, Salmon RJ, Thomas G, Dutrillaux B. Chromosome 12 alterations and c-Ki-ras mutations in colorectal tumors Cancer Genetics and Cytogenetics. 69: 161-162. PMID 8402559 DOI: 10.1016/0165-4608(93)90097-6 |
0.392 |
|
| 1993 |
Zucman J, Delattre O, Desmaze C, Epstein AL, Stenman G, Speleman F, Fletchers CDM, Aurias A, Thomas G. EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts. Nature Genetics. 4: 341-345. PMID 8401579 DOI: 10.1038/Ng0893-341 |
0.339 |
|
| 1993 |
Sanson M, Marineau C, Desmaze C, Lutchman M, Ruttledge M, Baron C, Narod S, Delattre O, Lenoir G, Thomas G, Aurlas A, Rouleau GA. Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus Human Molecular Genetics. 2: 1215-1220. PMID 8401504 DOI: 10.1093/Hmg/2.8.1215 |
0.469 |
|
| 1993 |
Rouleau GA, Merel P, Lutchman M, Sanson M, Zucman J, Marineau C, Hoang-Xuan K, Demczuk S, Desmaze C, Plougastel B, Pulst SM, Lenoir G, Bijlsma E, Fashold R, Dumanski J, ... ... Thomas G, et al. Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2 Nature. 363: 515-521. PMID 8379998 DOI: 10.1038/363515A0 |
0.427 |
|
| 1993 |
Plougastel B, Zucman J, Peter M, Thomas G, Delattre O. Genomic structure of the EWS gene and its relationship to EWSR1, a site of tumor-associated chromosome translocation Genomics. 18: 609-615. PMID 8307570 DOI: 10.1016/S0888-7543(05)80363-5 |
0.43 |
|
| 1993 |
Sanson M, Zhang F, Demczuk S, Delattre O, DeJong P, Aurias A, Thomas G, Rouleau GA. Isolation and mapping of 45 NotI linking clones to chromosome 22. Genomics. 17: 776-9. PMID 8244398 DOI: 10.1006/Geno.1993.1407 |
0.372 |
|
| 1993 |
Sorensen PH, Liu XF, Delattre O, Rowland JM, Biggs CA, Thomas G, Triche TJ. Reverse transcriptase PCR amplification of EWS/FLI-1 fusion transcripts as a diagnostic test for peripheral primitive neuroectodermal tumors of childhood. Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 2: 147-57. PMID 7506981 DOI: 10.1097/00019606-199300020-00024 |
0.386 |
|
| 1993 |
Bijlsma EK, Delattre O, Juyn JA, Melot T, Westerveld A, Dumanski JP, Thomas G, Hulsebos TJ. Regional fine mapping of the beta crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2. Genes, Chromosomes & Cancer. 8: 112-8. PMID 7504514 DOI: 10.1002/Gcc.2870080208 |
0.429 |
|
| 1992 |
Aubry M, Marineau C, Zhang FR, Zahed L, Figlewicz D, Delattre O, Thomas G, de Jong PJ, Julien JP, Rouleau GA. Cloning of six new genes with zinc finger motifs mapping to short and long arms of human acrocentric chromosome 22 (p and q11.2). Genomics. 13: 641-8. PMID 1639391 DOI: 10.1016/0888-7543(92)90135-F |
0.423 |
|
| 1992 |
Zucman J, Delattre O, Desmaze C, Azambuja C, Rouleau G, De Jong P, Aurias A, Thomas G. Rapid isolation of cosmids from defined subregions by differential Alu-PCR hybridization on chromosome 22-specific library. Genomics. 13: 395-401. PMID 1612598 DOI: 10.1016/0888-7543(92)90259-U |
0.381 |
|
| 1992 |
Desmaze C, Zucman J, Delattre O, Thomas G, Aurias A. In situ hybridization of PCR amplified inter-Alu sequences from a hybrid cell line. Human Genetics. 88: 541-544. PMID 1551656 DOI: 10.1007/Bf00219341 |
0.337 |
|
| 1992 |
Peter M, Michon J, Vielh P, Neuenschwander S, Nakamura Y, Sonsino E, Zucker JM, Vergnaud G, Thomas G, Delattre O. PCR assay for chromosome 1p deletion in small neuroblastoma samples. International Journal of Cancer. Journal International Du Cancer. 52: 544-8. PMID 1399134 DOI: 10.1002/Ijc.2910520408 |
0.401 |
|
| 1992 |
Sanson M, Richard S, Delattre O, Poliwka M, Mikol J, Philippon J, Thomas G. Allelic loss on chromosome 22 correlates with histopathological predictors of recurrence of meningiomas. International Journal of Cancer. Journal International Du Cancer. 50: 391-4. PMID 1346529 DOI: 10.1002/Ijc.2910500311 |
0.417 |
|
| 1992 |
Wehnert A, Cruts M, Backhovens H, Delabar JM, Thomas G, Broeckhoven CV. Dinucleotide repeat polymorphism at the D21S258 locus Human Molecular Genetics. 1: 449-449. PMID 1339475 DOI: 10.1093/Hmg/1.6.449 |
0.313 |
|
| 1992 |
Olschwang S, Fabre R, Laurent-Puig P, Vassal A, Hamelin B, Nakamura Y, Thomas G. Detection by DGGE of a new polymorphism closely linked to the adenomatous polyposis coli region. Human Genetics. 88: 658-60. PMID 1312993 DOI: 10.1007/Bf02265293 |
0.354 |
|
| 1992 |
Laurent-Puig P, Olschwang S, Delattre O, Remvikos Y, Asselain B, Melot T, Validire P, Muleris M, Girodet J, Salmon RJ, Thomas G. Survival and acquired genetic alterations in colorectal cancer. Gastroenterology. 102: 1136-1141. DOI: 10.1016/0016-5085(92)90749-O |
0.407 |
|
| 1991 |
Delattre O, Azambuja CJ, Aurias A, Zucman J, Peter M, Zhang F, Hors-Cayla MC, Rouleau G, Thomas G. Mapping of human chromosome 22 with a panel of somatic cell hybrids. Genomics. 9: 721-7. PMID 2037296 DOI: 10.1016/0888-7543(91)90366-M |
0.395 |
|
| 1991 |
Olschwang S, Laurent-Puig P, Vassal A, Salmon RJ, Thomas G. Characterization of a frequent polymorphism in the coding sequence of the Tp53 gene in colonic cancer patients and a control population Human Genetics. 86: 369-370. PMID 1999338 DOI: 10.1007/Bf00201836 |
0.314 |
|
| 1991 |
Bossy D, Milili M, Zucman J, Thomas G, Fougereau M, Schiff C. Organization and expression of the lambda-like genes that contribute to the mu-psi light chain complex in human pre-B cells. International Immunology. 3: 1081-90. PMID 1760403 DOI: 10.1093/Intimm/3.11.1081 |
0.341 |
|
| 1991 |
Laurent-Puig P, Olschwang S, Delattre O, Validire P, Melot T, Mosseri V, Salmon RJ, Thomas G. Association of Ki-ras mutation with differentiation and tumor-formation pathways in colorectal carcinoma International Journal of Cancer. 49: 220-223. PMID 1652568 DOI: 10.1002/Ijc.2910490213 |
0.321 |
|
| 1991 |
Olschwang S, Weiffenbach B, Laurent-puig P, Melot T, Vassal A, Falls K, Salmon RJ, Parc R, Strong L, Nakamura Y, Herrera L, Thomas G. Genetic characterization of the APC locus involved in familial adenomatous polyposis Gastroenterology. 101: 154-160. PMID 1646139 DOI: 10.1016/0016-5085(91)90472-W |
0.366 |
|
| 1990 |
Zhang FR, Aurias A, Delattre O, Stern MH, Benitez J, Rouleau G, Thomas G. Mapping of human chromosome 22 by in situ hybridization. Genomics. 7: 319-24. PMID 2365353 DOI: 10.1016/0888-7543(90)90164-P |
0.382 |
|
| 1990 |
Zhang FR, Delattre O, Rouleau G, Couturier J, Thomas G, Aurias A. The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus. Genomics. 6: 174-7. PMID 2303258 DOI: 10.1016/0888-7543(90)90463-5 |
0.392 |
|
| 1990 |
Muleris M, Delattre O, Olschwang S, Dutrillaux AM, Remvikos Y, Salmon RJ, Thomas G, Dutrillaux B. Cytogenetic and molecular approaches of polyploidization in colorectal adenocarcinomas Cancer Genetics and Cytogenetics. 44: 107-118. PMID 2293876 DOI: 10.1016/0165-4608(90)90203-M |
0.427 |
|
| 1990 |
Couturier J, Delattre O, Kujas M, Philippon J, Peter M, Rouleau G, Aurias A, Thomas G. Assessment of chromosome 22 anomalies in neurinomas by combined karyotype and RFLP analyses. Cancer Genetics and Cytogenetics. 45: 55-62. PMID 1967977 DOI: 10.1016/0165-4608(90)90066-J |
0.425 |
|
| 1989 |
Schmitz A, Olschwang S, Chaput B, Thomas G, Frelat G. Oncogene detection by enzymatic amplification on flow sorted chromosomes Nucleic Acids Research. 17: 816-816. PMID 2915937 DOI: 10.1093/Nar/17.2.816 |
0.324 |
|
| 1989 |
Lefrançois D, Olschwang S, Delattre O, Muleris M, Dutrillaux A, Thomas G, Dutrillaux B. Preservation of chromosome and DNA characteristics of human colorectal adenocarcinomas after passage in nude mice International Journal of Cancer. 44: 871-878. PMID 2573580 DOI: 10.1002/Ijc.2910440521 |
0.412 |
|
| 1989 |
Delattre O, Law DJ, Remvikos Y, Sastre X, Feinberg AP, Olschwang S, Melot T, Salmon RJ, Validire P, Thomas G. MULTIPLE GENETIC ALTERATIONS IN DISTAL AND PROXIMAL COLORECTAL CANCER The Lancet. 334: 353-356. PMID 2569552 DOI: 10.1016/S0140-6736(89)90537-0 |
0.384 |
|
| 1989 |
Delattre O, Gross M, Taud Md, Cong NV, Thomas G. RFLP identified by the anonymous DNA segment OLVIID1 on chromosome 6 [HGM9 no.D6S47]. Nucleic Acids Research. 17: 1789-1789. PMID 2466242 DOI: 10.1093/Nar/17.4.1789 |
0.347 |
|
| 1989 |
Stern M, Lipkowitz S, Aurias A, Griscelli C, Thomas G, Kirsch I. Inversion of chromosome 7 in ataxia telangiectasia is generated by a rearrangement between T-cell receptor beta and T-cell receptor gamma genes. Blood. 74: 2076-2080. DOI: 10.1182/Blood.V74.6.2076.2076 |
0.37 |
|
| 1989 |
Delattre O, Law D, Olschwang S, Melot T, Peter M, Sastre X, Validire P, Salmon R, Feinberg A, Thomas G. 113 Prevalence of allelic loss and Ki-ras mutation in colorectal tumors Cancer Genetics and Cytogenetics. 38: 195. DOI: 10.1016/0165-4608(89)90640-7 |
0.324 |
|
| 1988 |
Stern MH, Zhang FR, Griscelli C, Thomas G, Aurias A. Molecular characterization of different ataxia telangiectasia T-cell clones. I. A common breakpoint at the 14q11.2 band splits the T-cell receptor alpha-chain gene. Human Genetics. 78: 33-6. PMID 3422210 DOI: 10.1007/Bf00291230 |
0.368 |
|
| 1988 |
Monpezat J-, Delattre O, Bernard A, Grunwald D, Remvikos Y, Muleris M, Salmon RJ, Frelat G, Dutrillaux B, Thomas G. Loss of alleles on chromosome 18 and on the short arm of chromosome 17 in polyploid colorectal carcinomas. International Journal of Cancer. 41: 404-408. PMID 3346104 DOI: 10.1002/Ijc.2910410315 |
0.413 |
|
| 1988 |
Zhang F, Stern MH, Thomas G, Aurias A. Molecular characterization of ataxia telangiectasia T cell clones. II. The clonal inv(14) in ataxia telangiectasia differs from the inv(14) in T cell lymphoma. Human Genetics. 78: 316-9. PMID 3258841 DOI: 10.1007/Bf00291726 |
0.351 |
|
| 1988 |
Delattre O, Grunwald M, Bernard A, Grunwald D, Thomas G, Frelat G, Aurias A. Recurrent t(11;22) breakpoint mapping by chromosome flow sorting and spot-blot hybridization. Human Genetics. 78: 140-143. PMID 3123358 DOI: 10.1007/Bf00278184 |
0.416 |
|
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