| Year |
Citation |
Score |
| 2019 |
Zhang Y, Yang L, Kucherlapati M, Hadjipanayis A, Pantazi A, Bristow CA, Lee EA, Mahadeshwar HS, Tang J, Zhang J, Seth S, Lee S, Ren X, Song X, Sun H, ... ... Kucherlapati R, et al. Global impact of somatic structural variation on the DNA methylome of human cancers. Genome Biology. 20: 209. PMID 31610796 DOI: 10.1186/S13059-019-1818-9 |
0.392 |
|
| 2018 |
Zhang Y, Yang L, Kucherlapati M, Chen F, Hadjipanayis A, Pantazi A, Bristow CA, Lee EA, Mahadeshwar HS, Tang J, Zhang J, Seth S, Lee S, Ren X, Song X, ... ... Kucherlapati R, et al. A Pan-Cancer Compendium of Genes Deregulated by Somatic Genomic Rearrangement across More Than 1,400 Cases. Cell Reports. 24: 515-527. PMID 29996110 DOI: 10.1016/J.Celrep.2018.06.025 |
0.378 |
|
| 2017 |
Jahid S, Sun J, Gelincik O, Blecua P, Edelmann W, Kucherlapati R, Zhou K, Jasin M, Gümüş ZH, Lipkin SM. Inhibition of colorectal cancer genomic copy number alterations and chromosomal fragile site tumor suppressor FHIT and WWOX deletions by DNA mismatch repair. Oncotarget. 8: 71574-71586. PMID 29069730 DOI: 10.18632/Oncotarget.17776 |
0.396 |
|
| 2017 |
Zhang Y, Kwok-Shing Ng P, Kucherlapati M, Chen F, Liu Y, Tsang YH, de Velasco G, Jeong KJ, Akbani R, Hadjipanayis A, Pantazi A, Bristow CA, Lee E, Mahadeshwar HS, Tang J, ... ... Kucherlapati R, et al. A Pan-Cancer Proteogenomic Atlas of PI3K/AKT/mTOR Pathway Alterations. Cancer Cell. PMID 28528867 DOI: 10.1016/J.Ccell.2017.04.013 |
0.332 |
|
| 2017 |
Lu H, Villafane N, Dogruluk T, Grzeskowiak CL, Kong K, Tsang YH, Zagorodna O, Pantazi A, Yang L, Neill NJ, Kim YW, Creighton CJ, Verhaak RG, Mills GB, Park P, ... Kucherlapati RS, et al. Engineering and Functional Characterization of Fusion Genes Identifies Novel Oncogenic Drivers of Cancer. Cancer Research. PMID 28512244 DOI: 10.1158/0008-5472.Can-16-2745 |
0.366 |
|
| 2017 |
Cherniack AD, Shen H, Walter V, Stewart C, Murray BA, Bowlby R, Hu X, Ling S, Soslow RA, Broaddus RR, Zuna RE, Robertson G, Laird PW, Kucherlapati R, Mills GB, et al. Integrated Molecular Characterization of Uterine Carcinosarcoma. Cancer Cell. 31: 411-423. PMID 28292439 DOI: 10.1016/J.Ccell.2017.02.010 |
0.351 |
|
| 2016 |
Sun Y, Ji P, Chen T, Zhou X, Yang D, Guo Y, Liu Y, Hu L, Xia D, Liu Y, Multani AS, Shmulevich I, Kucherlapati R, Kopetz S, Sood AK, et al. MIIP haploinsufficiency induces chromosomal instability and promotes tumour progression in colorectal cancer. The Journal of Pathology. PMID 27741356 DOI: 10.1002/Path.4823 |
0.38 |
|
| 2016 |
Yang L, Lee MS, Lu H, Oh DY, Kim YJ, Park D, Park G, Ren X, Bristow CA, Haseley PS, Lee S, Pantazi A, Kucherlapati R, Park WY, Scott KL, et al. Analyzing Somatic Genome Rearrangements in Human Cancers by Using Whole-Exome Sequencing. American Journal of Human Genetics. 98: 843-856. PMID 27153396 DOI: 10.1016/J.Ajhg.2016.03.017 |
0.399 |
|
| 2016 |
Chen F, Zhang Y, Şenbabaoğlu Y, Ciriello G, Yang L, Reznik E, Shuch B, Micevic G, De Velasco G, Shinbrot E, Noble MS, Lu Y, Covington KR, Xi L, Drummond JA, ... ... Kucherlapati R, et al. Multilevel Genomics-Based Taxonomy of Renal Cell Carcinoma. Cell Reports. PMID 26947078 DOI: 10.1016/J.Celrep.2016.02.024 |
0.329 |
|
| 2016 |
Weinstein JN, Lerner SP, Kwiatkowski DJ, Getz G, Kim J, Al-ahmadie HA, Cherniack AD, Guo G, Akbani R, Hoadley KA, Kim WY, Robertson G, Mungall AJ, Hinoue T, Laird PW, ... ... Kucherlapati R, et al. Abstract 128: Comprehensive molecular characterization of 412 muscle-invasive urothelial bladder carcinomas: final analysis of The Cancer Genome Atlas (TCGA) project Cancer Research. 76: 128-128. DOI: 10.1158/1538-7445.Am2016-128 |
0.356 |
|
| 2014 |
Davis CF, Ricketts CJ, Wang M, Yang L, Cherniack AD, Shen H, Buhay C, Kang H, Kim SC, Fahey CC, Hacker KE, Bhanot G, Gordenin DA, Chu A, Gunaratne PH, ... ... Kucherlapati R, et al. The somatic genomic landscape of chromophobe renal cell carcinoma. Cancer Cell. 26: 319-30. PMID 25155756 DOI: 10.1016/J.Ccr.2014.07.014 |
0.339 |
|
| 2014 |
Chen PC, Yin J, Yu HW, Yuan T, Fernandez M, Yung CK, Trinh QM, Peltekova VD, Reid JG, Tworog-Dube E, Morgan MB, Muzny DM, Stein L, McPherson JD, Roberts AE, ... ... Kucherlapati R, et al. Next-generation sequencing identifies rare variants associated with Noonan syndrome. Proceedings of the National Academy of Sciences of the United States of America. 111: 11473-8. PMID 25049390 DOI: 10.1073/Pnas.1324128111 |
0.335 |
|
| 2014 |
Weinstein JN, Kim J, Creighton CJ, Akbani R, Hoadley KA, Kim WY, Morgan MB, Hinoue T, Rosenberg JE, Bajorin DF, Hansel DE, Al-Ahmadie H, Gordenin D, Stuart JM, Robertson G, ... Kucherlapati R, et al. Comprehensive molecular profiling of urothelial bladder cancer at the DNA, RNA, and protein levels: A TCGA project. Journal of Clinical Oncology. 32: 4509-4509. DOI: 10.1200/Jco.2014.32.15_Suppl.4509 |
0.37 |
|
| 2014 |
Weinstein JN, Kim J, Creighton CJ, Akbani R, Hoadley KA, Kim WY, Morgan MB, Hinoue T, Cherniack A, Su X, Mungall AJ, Ryan MC, Rosenberg JE, Bajorin DF, Czerniak B, ... ... Kucherlapati R, et al. Abstract 987: Comprehensive characterization of urothelial bladder cancer: a TCGA Project update Cancer Research. 74: 987-987. DOI: 10.1158/1538-7445.Am2014-987 |
0.353 |
|
| 2014 |
Yang L, Luquette LJ, Gehlenborg N, Xi R, Haseley PS, Hsieh CH, Zhang C, Ren X, Protopopov A, Chin L, Kucherlapati R, Lee C, Park PJ. Erratum: Diverse mechanisms of somatic structural variations in human cancer genomes (Cell (2013) 153 (919-929)) Cell. 157. DOI: 10.1016/J.Cell.2014.05.020 |
0.316 |
|
| 2013 |
Kucherlapati R, Leinwand LA. Frank Ruddle (1929-2013). American Journal of Human Genetics. 92: 839-40. PMID 24242788 DOI: 10.1016/J.Ajhg.2013.05.012 |
0.565 |
|
| 2013 |
Brennan CW, Verhaak RG, McKenna A, Campos B, Noushmehr H, Salama SR, Zheng S, Chakravarty D, Sanborn JZ, Berman SH, Beroukhim R, Bernard B, Wu CJ, Genovese G, Shmulevich I, ... ... Kucherlapati R, et al. The somatic genomic landscape of glioblastoma. Cell. 155: 462-77. PMID 24120142 DOI: 10.1016/J.Cell.2013.09.034 |
0.334 |
|
| 2013 |
Kucherlapati R. Francis H. Ruddle (1929-2013): a pioneer in human gene mapping. Proceedings of the National Academy of Sciences of the United States of America. 110: 9619-20. PMID 23716665 DOI: 10.1073/Pnas.1308094110 |
0.399 |
|
| 2013 |
Yang L, Luquette LJ, Gehlenborg N, Xi R, Haseley PS, Hsieh CH, Zhang C, Ren X, Protopopov A, Chin L, Kucherlapati R, Lee C, Park PJ. Diverse mechanisms of somatic structural variations in human cancer genomes. Cell. 153: 919-29. PMID 23663786 DOI: 10.1016/J.Cell.2013.04.010 |
0.328 |
|
| 2013 |
Kandoth C, Schultz N, Cherniack AD, Akbani R, Liu Y, Shen H, Robertson AG, Pashtan I, Shen R, Benz CC, Yau C, Laird PW, Ding L, Zhang W, ... ... Kucherlapati R, et al. Integrated genomic characterization of endometrial carcinoma. Nature. 497: 67-73. PMID 23636398 DOI: 10.1038/Nature12113 |
0.308 |
|
| 2012 |
Kovalenko M, Dragileva E, St Claire J, Gillis T, Guide JR, New J, Dong H, Kucherlapati R, Kucherlapati MH, Ehrlich ME, Lee JM, Wheeler VC. Msh2 acts in medium-spiny striatal neurons as an enhancer of CAG instability and mutant huntingtin phenotypes in Huntington's disease knock-in mice. Plos One. 7: e44273. PMID 22970194 DOI: 10.1371/Journal.Pone.0044273 |
0.327 |
|
| 2012 |
Larman TC, DePalma SR, Hadjipanayis AG, Protopopov A, Zhang J, Gabriel SB, Chin L, Seidman CE, Kucherlapati R, Seidman JG. Spectrum of somatic mitochondrial mutations in five cancers. Proceedings of the National Academy of Sciences of the United States of America. 109: 14087-91. PMID 22891333 DOI: 10.1073/Pnas.1211502109 |
0.317 |
|
| 2012 |
Lee E, Iskow R, Yang L, Gokcumen O, Haseley P, Luquette LJ, Lohr JG, Harris CC, Ding L, Wilson RK, Wheeler DA, Gibbs RA, Kucherlapati R, Lee C, Kharchenko PV, et al. Landscape of somatic retrotransposition in human cancers. Science (New York, N.Y.). 337: 967-71. PMID 22745252 DOI: 10.1126/Science.1222077 |
0.363 |
|
| 2012 |
Kucherlapati R. Genetically modified mouse models for biomarker discovery and preclinical drug testing. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 18: 625-30. PMID 22298895 DOI: 10.1158/1078-0432.Ccr-11-2021 |
0.375 |
|
| 2012 |
Lee E, Iskow R, Yang L, Gokcumen O, Haseley P, Luquette LJ, Lohr JG, Harris CC, Ding L, Wilson RK, Wheeler DA, Gibbs RA, Kucherlapati R, Lee C, Kharchenko PV, et al. Analysis of somatic retrotransposition in human cancers Bmc Proceedings. 6. DOI: 10.1186/1753-6561-6-S6-O23 |
0.305 |
|
| 2012 |
Koboldt DC, Fulton RS, McLellan MD, Schmidt H, Kalicki-Veizer J, McMichael JF, Fulton LL, Dooling DJ, Ding L, Mardis ER, Wilson RK, Ally A, Balasundaram M, Butterfield YSN, Carlsen R, ... ... Kucherlapati R, et al. Comprehensive molecular portraits of human breast tumours Nature. 490: 61-70. DOI: 10.1038/Nature11412 |
0.311 |
|
| 2011 |
Hiramoto T, Kang G, Suzuki G, Satoh Y, Kucherlapati R, Watanabe Y, Hiroi N. Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model. Human Molecular Genetics. 20: 4775-85. PMID 21908517 DOI: 10.1093/Hmg/Ddr404 |
0.617 |
|
| 2010 |
Chen PC, Wakimoto H, Conner D, Araki T, Yuan T, Roberts A, Seidman C, Bronson R, Neel B, Seidman JG, Kucherlapati R. Activation of multiple signaling pathways causes developmental defects in mice with a Noonan syndrome–associated Sos1 mutation. The Journal of Clinical Investigation. 120: 4353-65. PMID 21041952 DOI: 10.1172/Jci43910 |
0.315 |
|
| 2010 |
Wang Y, Zhang W, Edelmann L, Kolodner RD, Kucherlapati R, Edelmann W. Cis lethal genetic interactions attenuate and alter p53 tumorigenesis. Proceedings of the National Academy of Sciences of the United States of America. 107: 5511-5. PMID 20212136 DOI: 10.1073/Pnas.1001223107 |
0.327 |
|
| 2010 |
Hung KE, Maricevich MA, Richard LG, Chen WY, Richardson MP, Kunin A, Bronson RT, Mahmood U, Kucherlapati R. Development of a mouse model for sporadic and metastatic colon tumors and its use in assessing drug treatment. Proceedings of the National Academy of Sciences of the United States of America. 107: 1565-70. PMID 20080688 DOI: 10.1073/Pnas.0908682107 |
0.326 |
|
| 2010 |
Kucherlapati MH, Lee K, Nguyen AA, Clark AB, Hou H, Rosulek A, Li H, Yang K, Fan K, Lipkin M, Bronson RT, Jelicks L, Kunkel TA, Kucherlapati R, Edelmann W. An Msh2 conditional knockout mouse for studying intestinal cancer and testing anticancer agents. Gastroenterology. 138: 993-1002.e1. PMID 19931261 DOI: 10.1053/J.Gastro.2009.11.009 |
0.356 |
|
| 2010 |
Baba Y, Shima K, Nosho K, Chung DC, Hung KE, Mahmood U, Kucherlapati R, Fuchs CS, Ogino S, Chan AT. S1935 Cathepsin B Expression and Survival After Diagnosis of Colorectal Cancer Gastroenterology. 138. DOI: 10.1016/S0016-5085(10)61306-6 |
0.346 |
|
| 2009 |
Itano O, Yang K, Fan K, Kurihara N, Shinozaki H, Abe S, Jin B, Gravaghi C, Edelmann W, Augenlicht L, Kopelovich L, Kucherlapati R, Lamprecht S, Lipkin M. Sulindac effects on inflammation and tumorigenesis in the intestine of mice with Apc and Mlh1 mutations. Carcinogenesis. 30: 1923-6. PMID 19755659 DOI: 10.1093/Carcin/Bgp200 |
0.326 |
|
| 2009 |
Suzuki G, Harper KM, Hiramoto T, Funke B, Lee M, Kang G, Buell M, Geyer MA, Kucherlapati R, Morrow B, Männistö PT, Agatsuma S, Hiroi N. Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice. Human Molecular Genetics. 18: 3914-25. PMID 19617637 DOI: 10.1093/Hmg/Ddp334 |
0.594 |
|
| 2009 |
Herman DS, Hovingh GK, Iartchouk O, Rehm HL, Kucherlapati R, Seidman JG, Seidman CE. Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection. Nature Methods. 6: 507-10. PMID 19543287 DOI: 10.1038/Nmeth.1343 |
0.322 |
|
| 2009 |
Kuraguchi M, Ohene-Baah NY, Sonkin D, Bronson RT, Kucherlapati R. Genetic mechanisms in Apc-mediated mammary tumorigenesis. Plos Genetics. 5: e1000367. PMID 19197353 DOI: 10.1371/Journal.Pgen.1000367 |
0.327 |
|
| 2009 |
Dragileva E, Hendricks A, Teed A, Gillis T, Lopez ET, Friedberg EC, Kucherlapati R, Edelmann W, Lunetta KL, MacDonald ME, Wheeler VC. Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes. Neurobiology of Disease. 33: 37-47. PMID 18930147 DOI: 10.1016/J.Nbd.2008.09.014 |
0.305 |
|
| 2009 |
Hiramoto T, Suzuki G, Kang G, Funke B, Watanabe Y, Kucherlapati R, Morrow B, Hiroi N. Tbx1 heterozygosity impairs working memory in mice Neuroscience Research. 65: S121-S122. DOI: 10.1016/J.Neures.2009.09.576 |
0.502 |
|
| 2008 |
Montgomery KT, Iartchouck O, Li L, Loomis S, Obourn V, Kucherlapati R. PolyPhred analysis software for mutation detection from fluorescence-based sequence data. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 7.16. PMID 18972372 DOI: 10.1002/0471142905.Hg0716S59 |
0.31 |
|
| 2008 |
Kucherlapati MH, Yang K, Fan K, Kuraguchi M, Sonkin D, Rosulek A, Lipkin M, Bronson RT, Aronow BJ, Kucherlapati R. Loss of Rb1 in the gastrointestinal tract of Apc1638N mice promotes tumors of the cecum and proximal colon. Proceedings of the National Academy of Sciences of the United States of America. 105: 15493-8. PMID 18832169 DOI: 10.1073/Pnas.0802933105 |
0.327 |
|
| 2008 |
Chen PC, Kuraguchi M, Velasquez J, Wang Y, Yang K, Edwards R, Gillen D, Edelmann W, Kucherlapati R, Lipkin SM. Novel roles for MLH3 deficiency and TLE6-like amplification in DNA mismatch repair-deficient gastrointestinal tumorigenesis and progression. Plos Genetics. 4: e1000092. PMID 18551179 DOI: 10.1371/Journal.Pgen.1000092 |
0.351 |
|
| 2008 |
Barrera-Oro J, Liu TY, Gorden E, Kucherlapati R, Shao C, Tischfield JA. Role of the mismatch repair gene, Msh6, in suppressing genome instability and radiation-induced mutations. Mutation Research. 642: 74-9. PMID 18538799 DOI: 10.1016/J.Mrfmmm.2008.04.006 |
0.355 |
|
| 2008 |
Montgomery KT, Iartchouck O, Li L, Perera A, Yassin Y, Tamburino A, Loomis S, Kucherlapati R. Mutation detection using automated fluorescence-based sequencing. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit7.9. PMID 18428426 DOI: 10.1002/0471142905.Hg0709S57 |
0.309 |
|
| 2008 |
Busuttil RA, Lin Q, Stambrook PJ, Kucherlapati R, Vijg J. Mutation frequencies and spectra in DNA polymerase eta-deficient mice. Cancer Research. 68: 2081-4. PMID 18381412 DOI: 10.1158/0008-5472.Can-07-6274 |
0.352 |
|
| 2008 |
Avdievich E, Reiss C, Scherer SJ, Zhang Y, Maier SM, Jin B, Hou H, Rosenwald A, Riedmiller H, Kucherlapati R, Cohen PE, Edelmann W, Kneitz B. Distinct effects of the recurrent Mlh1G67R mutation on MMR functions, cancer, and meiosis. Proceedings of the National Academy of Sciences of the United States of America. 105: 4247-52. PMID 18337503 DOI: 10.1073/Pnas.0800276105 |
0.368 |
|
| 2008 |
Swanson KD, Winter JM, Reis M, Bentires-Alj M, Greulich H, Grewal R, Hruban RH, Yeo CJ, Yassin Y, Iartchouk O, Montgomery K, Whitman SP, Caligiuri MA, Loh ML, Gilliland DG, ... ... Kucherlapati R, et al. SOS1 mutations are rare in human malignancies: implications for Noonan Syndrome patients. Genes, Chromosomes & Cancer. 47: 253-9. PMID 18064648 DOI: 10.1002/Gcc.20527 |
0.343 |
|
| 2007 |
Forrester S, Hung KE, Kuick R, Kucherlapati R, Haab BB. Low-volume, high-throughput sandwich immunoassays for profiling plasma proteins in mice: identification of early-stage systemic inflammation in a mouse model of intestinal cancer. Molecular Oncology. 1: 216-25. PMID 19305640 DOI: 10.1016/J.Molonc.2007.06.001 |
0.303 |
|
| 2007 |
Lencz T, Lambert C, DeRosse P, Burdick KE, Morgan TV, Kane JM, Kucherlapati R, Malhotra AK. Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America. 104: 19942-7. PMID 18077426 DOI: 10.1073/Pnas.0710021104 |
0.316 |
|
| 2007 |
Martin ES, Tonon G, Sinha R, Xiao Y, Feng B, Kimmelman AC, Protopopov A, Ivanova E, Brennan C, Montgomery K, Kucherlapati R, Bailey G, Redston M, Chin L, DePinho RA. Common and distinct genomic events in sporadic colorectal cancer and diverse cancer types. Cancer Research. 67: 10736-43. PMID 18006816 DOI: 10.1158/0008-5472.Can-07-2742 |
0.379 |
|
| 2007 |
Lencz T, Morgan TV, Athanasiou M, Dain B, Reed CR, Kane JM, Kucherlapati R, Malhotra AK. Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia. Molecular Psychiatry. 12: 572-80. PMID 17522711 DOI: 10.1038/Sj.Mp.4001983 |
0.317 |
|
| 2007 |
Funke BH, Brown AC, Ramoni MF, Regan ME, Baglieri C, Finn CT, Babcock M, Shprintzen RJ, Morrow BE, Kucherlapati R. A novel, single nucleotide polymorphism-based assay to detect 22q11 deletions. Genetic Testing. 11: 91-100. PMID 17394398 DOI: 10.1089/Gte.2006.0507 |
0.352 |
|
| 2007 |
Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, Li L, Yassin Y, Tamburino AM, Neel BG, Kucherlapati RS. Germline gain-of-function mutations in SOS1 cause Noonan syndrome. Nature Genetics. 39: 70-4. PMID 17143285 DOI: 10.1038/Ng1926 |
0.316 |
|
| 2007 |
Joshi VA, Roberts AE, Kucherlapati RS. Noonan syndrome associated congenital hypertrophic cardiomyopathy and the role of sarcomere gene mutations Progress in Pediatric Cardiology. 24: 75-76. DOI: 10.1016/J.Ppedcard.2007.08.009 |
0.338 |
|
| 2006 |
Dumstorf CA, Clark AB, Lin Q, Kissling GE, Yuan T, Kucherlapati R, McGregor WG, Kunkel TA. Participation of mouse DNA polymerase iota in strand-biased mutagenic bypass of UV photoproducts and suppression of skin cancer. Proceedings of the National Academy of Sciences of the United States of America. 103: 18083-8. PMID 17114294 DOI: 10.1073/Pnas.0605247103 |
0.305 |
|
| 2006 |
Lee DG, Urbach JM, Wu G, Liberati NT, Feinbaum RL, Miyata S, Diggins LT, He J, Saucier M, Déziel E, Friedman L, Li L, Grills G, Montgomery K, Kucherlapati R, et al. Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial. Genome Biology. 7: R90. PMID 17038190 DOI: 10.1186/Gb-2006-7-10-R90 |
0.31 |
|
| 2006 |
Kuraguchi M, Wang XP, Bronson RT, Rothenberg R, Ohene-Baah NY, Lund JJ, Kucherlapati M, Maas RL, Kucherlapati R. Adenomatous polyposis coli (APC) is required for normal development of skin and thymus. Plos Genetics. 2: e146. PMID 17002498 DOI: 10.1371/Journal.Pgen.0020146 |
0.34 |
|
| 2006 |
Long JM, LaPorte P, Merscher S, Funke B, Saint-Jore B, Puech A, Kucherlapati R, Morrow BE, Skoultchi AI, Wynshaw-Boris A. Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome. Neurogenetics. 7: 247-57. PMID 16900388 DOI: 10.1007/S10048-006-0054-0 |
0.394 |
|
| 2006 |
Scherer SE, Muzny DM, Buhay CJ, Chen R, Cree A, Ding Y, Dugan-Rocha S, Gill R, Gunaratne P, Harris RA, Hawes AC, Hernandez J, Hodgson AV, Hume J, Jackson A, ... ... Kucherlapati R, et al. The finished DNA sequence of human chromosome 12. Nature. 440: 346-51. PMID 16541075 DOI: 10.1038/Nature04569 |
0.447 |
|
| 2006 |
Kates WR, Antshel KM, Abdulsabur N, Colgan D, Funke B, Fremont W, Higgins AM, Kucherlapati R, Shprintzen RJ. A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome). American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 274-80. PMID 16511839 DOI: 10.1002/Ajmg.B.30284 |
0.345 |
|
| 2006 |
Moran JL, Bolton AD, Tran PV, Brown A, Dwyer ND, Manning DK, Bjork BC, Li C, Montgomery K, Siepka SM, Vitaterna MH, Takahashi JS, Wiltshire T, Kwiatkowski DJ, Kucherlapati R, et al. Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse. Genome Research. 16: 436-40. PMID 16461637 DOI: 10.1101/Gr.4563306 |
0.357 |
|
| 2006 |
Burdick KE, Lencz T, Funke B, Finn CT, Szeszko PR, Kane JM, Kucherlapati R, Malhotra AK. Genetic variation in DTNBP1 influences general cognitive ability. Human Molecular Genetics. 15: 1563-8. PMID 16415041 DOI: 10.1093/Hmg/Ddi481 |
0.303 |
|
| 2006 |
Lin Q, Clark AB, McCulloch SD, Yuan T, Bronson RT, Kunkel TA, Kucherlapati R. Increased susceptibility to UV-induced skin carcinogenesis in polymerase eta-deficient mice. Cancer Research. 66: 87-94. PMID 16397220 DOI: 10.1158/0008-5472.Can-05-1862 |
0.306 |
|
| 2005 |
Hiroi N, Zhu H, Lee M, Funke B, Arai M, Itokawa M, Kucherlapati R, Morrow B, Sawamura T, Agatsuma S. A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice. Proceedings of the National Academy of Sciences of the United States of America. 102: 19132-7. PMID 16365290 DOI: 10.1073/Pnas.0509635102 |
0.614 |
|
| 2005 |
Ziv S, Brenner O, Amariglio N, Smorodinsky NI, Galron R, Carrion DV, Zhang W, Sharma GG, Pandita RK, Agarwal M, Elkon R, Katzin N, Bar-Am I, Pandita TK, Kucherlapati R, et al. Impaired genomic stability and increased oxidative stress exacerbate different features of Ataxia-telangiectasia. Human Molecular Genetics. 14: 2929-43. PMID 16150740 DOI: 10.1093/Hmg/Ddi324 |
0.37 |
|
| 2005 |
Lai WR, Johnson MD, Kucherlapati R, Park PJ. Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data. Bioinformatics (Oxford, England). 21: 3763-70. PMID 16081473 DOI: 10.1093/Bioinformatics/Bti611 |
0.338 |
|
| 2005 |
Wang Y, Putnam CD, Kane MF, Zhang W, Edelmann L, Russell R, Carrión DV, Chin L, Kucherlapati R, Kolodner RD, Edelmann W. Mutation in Rpa1 results in defective DNA double-strand break repair, chromosomal instability and cancer in mice. Nature Genetics. 37: 750-5. PMID 15965476 DOI: 10.1038/Ng1587 |
0.419 |
|
| 2005 |
Yang K, Fan KH, Lamprecht SA, Edelmann W, Kopelovich L, Kucherlapati R, Lipkin M. Peroxisome proliferator-activated receptor gamma agonist troglitazone induces colon tumors in normal C57BL/6J mice and enhances colonic carcinogenesis in Apc1638 N/+ Mlh1+/- double mutant mice. International Journal of Cancer. Journal International Du Cancer. 116: 495-9. PMID 15818612 DOI: 10.1002/Ijc.21018 |
0.311 |
|
| 2005 |
Roberts AE, Hult B, Rehm HL, Rehm HL, McDonough B, Barr S, Seidman CE, Seidman JG, Kucherlapati RS. The PTPN11 gene is not implicated in nonsyndromic hypertrophic cardiomyopathy. American Journal of Medical Genetics. Part A. 132: 333-4. PMID 15578621 DOI: 10.1002/Ajmg.A.30405 |
0.347 |
|
| 2004 |
Shao C, Deng L, Chen Y, Kucherlapati R, Stambrook PJ, Tischfield JA. Mlh1 mediates tissue-specific regulation of mitotic recombination. Oncogene. 23: 9017-24. PMID 15480418 DOI: 10.1038/Sj.Onc.1208148 |
0.357 |
|
| 2004 |
Yang G, Scherer SJ, Shell SS, Yang K, Kim M, Lipkin M, Kucherlapati R, Kolodner RD, Edelmann W. Dominant effects of an Msh6 missense mutation on DNA repair and cancer susceptibility. Cancer Cell. 6: 139-50. PMID 15324697 DOI: 10.1016/J.Ccr.2004.06.024 |
0.31 |
|
| 2004 |
Lin DP, Wang Y, Scherer SJ, Clark AB, Yang K, Avdievich E, Jin B, Werling U, Parris T, Kurihara N, Umar A, Kucherlapati R, Lipkin M, Kunkel TA, Edelmann W. An Msh2 point mutation uncouples DNA mismatch repair and apoptosis. Cancer Research. 64: 517-22. PMID 14744764 DOI: 10.1158/0008-5472.Can-03-2957 |
0.335 |
|
| 2003 |
Kabbarah O, Mallon MA, Pfeifer JD, Edelmann W, Kucherlapati R, Goodfellow PJ. A panel of repeat markers for detection of microsatellite instability in murine tumors. Molecular Carcinogenesis. 38: 155-9. PMID 14639654 DOI: 10.1002/Mc.10157 |
0.348 |
|
| 2003 |
Pretlow TP, Edelmann W, Kucherlapati R, Pretlow TG, Augenlicht LH. Spontaneous aberrant crypt foci in Apc1638N mice with a mutant Apc allele. The American Journal of Pathology. 163: 1757-63. PMID 14578176 DOI: 10.1016/S0002-9440(10)63535-3 |
0.35 |
|
| 2003 |
Supavekin S, Zhang W, Kucherlapati R, Kaskel FJ, Moore LC, Devarajan P. Differential gene expression following early renal ischemia/reperfusion. Kidney International. 63: 1714-24. PMID 12675847 DOI: 10.1046/J.1523-1755.2003.00928.X |
0.305 |
|
| 2002 |
Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M, An P, Antonarakis SE, Attwood J, Baertsch R, Bailey J, ... ... Kucherlapati RS, et al. Initial sequencing and comparative analysis of the mouse genome. Nature. 420: 520-62. PMID 12466850 DOI: 10.1038/Nature01262 |
0.305 |
|
| 2002 |
Kochilas L, Merscher-Gomez S, Lu MM, Potluri V, Liao J, Kucherlapati R, Morrow B, Epstein JA. The role of neural crest during cardiac development in a mouse model of DiGeorge syndrome. Developmental Biology. 251: 157-66. PMID 12413905 DOI: 10.1006/Dbio.2002.0819 |
0.359 |
|
| 2002 |
Kucherlapati M, Yang K, Kuraguchi M, Zhao J, Lia M, Heyer J, Kane MF, Fan K, Russell R, Brown AM, Kneitz B, Edelmann W, Kolodner RD, Lipkin M, Kucherlapati R. Haploinsufficiency of Flap endonuclease (Fen1) leads to rapid tumor progression. Proceedings of the National Academy of Sciences of the United States of America. 99: 9924-9. PMID 12119409 DOI: 10.1073/Pnas.152321699 |
0.394 |
|
| 2002 |
Wei K, Kucherlapati R, Edelmann W. Mouse models for human DNA mismatch-repair gene defects. Trends in Molecular Medicine. 8: 346-53. PMID 12114115 DOI: 10.1016/S1471-4914(02)02359-6 |
0.402 |
|
| 2002 |
Desai KV, Xiao N, Wang W, Gangi L, Greene J, Powell JI, Dickson R, Furth P, Hunter K, Kucherlapati R, Simon R, Liu ET, Green JE. Initiating oncogenic event determines gene-expression patterns of human breast cancer models. Proceedings of the National Academy of Sciences of the United States of America. 99: 6967-72. PMID 12011455 DOI: 10.1073/Pnas.102172399 |
0.356 |
|
| 2002 |
Tartaglia M, Kalidas K, Shaw A, Song X, Musat DL, van der Burgt I, Brunner HG, Bertola DR, Crosby A, Ion A, Kucherlapati RS, Jeffery S, Patton MA, Gelb BD. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. American Journal of Human Genetics. 70: 1555-63. PMID 11992261 DOI: 10.1086/340847 |
0.316 |
|
| 2002 |
Wang H, Douglas W, Lia M, Edelmann W, Kucherlapati R, Podsypanina K, Parsons R, Ellenson LH. DNA mismatch repair deficiency accelerates endometrial tumorigenesis in Pten heterozygous mice. The American Journal of Pathology. 160: 1481-6. PMID 11943731 DOI: 10.1016/S0002-9440(10)62573-4 |
0.303 |
|
| 2001 |
Tartaglia M, Mehler EL, Goldberg R, Zampino G, Brunner HG, Kremer H, van der Burgt I, Crosby AH, Ion A, Jeffery S, Kalidas K, Patton MA, Kucherlapati RS, Gelb BD. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nature Genetics. 29: 465-8. PMID 11704759 DOI: 10.1038/Ng772 |
0.354 |
|
| 2001 |
Kucherlapati R, DePinho RA. Cancer. Telomerase meets its mismatch. Nature. 411: 647-8. PMID 11395749 DOI: 10.1038/35079715 |
0.346 |
|
| 2001 |
Merscher S, Funke B, Epstein JA, Heyer J, Puech A, Lu MM, Xavier RJ, Demay MB, Russell RG, Factor S, Tokooya K, Jore BS, Lopez M, Pandita RK, Lia M, ... ... Kucherlapati R, et al. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome. Cell. 104: 619-29. PMID 11239417 DOI: 10.1016/S0092-8674(01)00247-1 |
0.401 |
|
| 2001 |
Montgomery KT, Lee E, Miller A, Lau S, Shim C, Decker J, Chiu D, Emerling S, Sekhon M, Kim R, Lenz J, Han J, Ioshikhes I, Renault B, Marondel I, ... ... Kucherlapati R, et al. A high-resolution map of human chromosome 12. Nature. 409: 945-6. PMID 11237017 DOI: 10.1038/35057174 |
0.358 |
|
| 2001 |
Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W, Funke R, Gage D, Harris K, Heaford A, Howland J, ... ... Kucherlapati RS, et al. Initial sequencing and analysis of the human genome. Nature. 409: 860-921. PMID 11237011 DOI: 10.1038/35057062 |
0.306 |
|
| 2001 |
Tartaglia M, Mehler E, Goldberg R, Zampino G, Brunner H, Kremer H, van der Burgt I, Crosby A, Ion A, Jeffery S, Kalidas K, Patton M, Kucherlapati R, Gelb B. Correction: Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan syndrome Nature Genetics. 29: 491-491. DOI: 10.1038/Ng1201-491C |
0.313 |
|
| 2001 |
Bourdon V, Mhlanga MM, Massimi A, Tyagi S, Kucherlapati R, Chaganti RS. A 12p array to identify amplified and overexpressed sequences in testicular germ cell tumors Nature Genetics. 27: 44-44. DOI: 10.1038/87016 |
0.339 |
|
| 2000 |
Ion A, Crosby AH, Kremer H, Kenmochi N, Van Reen M, Fenske C, Van Der Burgt I, Brunner HG, Montgomery K, Kucherlapati RS, Patton MA, Page C, Mariman E, Jeffery S. Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6. Journal of Medical Genetics. 37: 884-6. PMID 11185075 DOI: 10.1136/Jmg.37.11.884 |
0.436 |
|
| 2000 |
Kuraguchi M, Edelmann W, Yang K, Lipkin M, Kucherlapati R, Brown AM. Tumor-associated Apc mutations in Mlh1-/- Apc1638N mice reveal a mutational signature of Mlh1 deficiency. Oncogene. 19: 5755-63. PMID 11126362 DOI: 10.1038/Sj.Onc.1203962 |
0.316 |
|
| 2000 |
Lee SG, Cho KA, Choi YH, Montgomery K, Lee E, Miller A, Kucherlapati R, Song K. A sequence-ready map for human chromosome 12q15-21. Dna Sequence : the Journal of Dna Sequencing and Mapping. 11: 353-61. PMID 11092752 DOI: 10.3109/10425170009033255 |
0.372 |
|
| 2000 |
Lee H, Choi E, Seomun Y, Montgomery K, Huebner A, Lee E, Lau S, Joo CK, Kucherlapati R, Yoon SJ. High-resolution transcript map of the region spanning D12S1629 and D12S312 at chromosome 12q13: triple A syndrome-linked region. Genome Research. 10: 1561-7. PMID 11042153 DOI: 10.1101/Gr.142100 |
0.43 |
|
| 2000 |
Smits R, Hofland N, Edelmann W, Geugien M, Jagmohan-Changur S, Albuquerque C, Breukel C, Kucherlapati R, Kielman MF, Fodde R. Somatic Apc mutations are selected upon their capacity to inactivate the beta-catenin downregulating activity. Genes, Chromosomes & Cancer. 29: 229-39. PMID 10992298 DOI: 10.1002/1098-2264(2000)9999:9999<::Aid-Gcc1033>3.0.Co;2-R |
0.315 |
|
| 2000 |
Casey M, Vaughan CJ, He J, Hatcher CJ, Winter JM, Weremowicz S, Montgomery K, Kucherlapati R, Morton CC, Basson CT. Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex. The Journal of Clinical Investigation. 106: R31-8. PMID 10974026 DOI: 10.1172/Jci10841 |
0.395 |
|
| 2000 |
Peyron C, Faraco J, Rogers W, Ripley B, Overeem S, Charnay Y, Nevsimalova S, Aldrich M, Reynolds D, Albin R, Li R, Hungs M, Pedrazzoli M, Padigaru M, Kucherlapati M, ... ... Kucherlapati R, et al. A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains. Nature Medicine. 6: 991-7. PMID 10973318 DOI: 10.1038/79690 |
0.315 |
|
| 2000 |
Puech A, Saint-Jore B, Merscher S, Russell RG, Cherif D, Sirotkin H, Xu H, Factor S, Kucherlapati R, Skoultchi AI. Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region. Proceedings of the National Academy of Sciences of the United States of America. 97: 10090-5. PMID 10963672 DOI: 10.1073/Pnas.97.18.10090 |
0.749 |
|
| 2000 |
Bala S, Oliver H, Renault B, Montgomery K, Dutta S, Rao P, Houldsworth J, Kucherlapati R, Wang X, Chaganti RS, Murty VV. Genetic analysis of the APAF1 gene in male germ cell tumors. Genes, Chromosomes & Cancer. 28: 258-68. PMID 10862031 DOI: 10.1002/1098-2264(200007)28:3<258::Aid-Gcc3>3.0.Co;2-R |
0.474 |
|
| 2000 |
Kneitz B, Cohen PE, Avdievich E, Zhu L, Kane MF, Hou H, Kolodner RD, Kucherlapati R, Pollard JW, Edelmann W. MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice. Genes & Development. 14: 1085-97. PMID 10809667 DOI: 10.1101/Gad.14.9.1085 |
0.391 |
|
| 2000 |
Pellegata NS, Dieguez-Lucena JL, Joensuu T, Lau S, Montgomery KT, Krahe R, Kivelä T, Kucherlapati R, Forsius H, de la Chapelle A. Mutations in KERA, encoding keratocan, cause cornea plana. Nature Genetics. 25: 91-5. PMID 10802664 DOI: 10.1038/75664 |
0.368 |
|
| 2000 |
Renedo M, Arce I, Montgomery K, Roda-Navarro P, Lee E, Kucherlapati R, Fernández-Ruiz E. A sequence-ready physical map of the region containing the human natural killer gene complex on chromosome 12p12.3-p13.2. Genomics. 65: 129-36. PMID 10783260 DOI: 10.1006/Geno.2000.6163 |
0.422 |
|
| 2000 |
Roda-Navarro P, Arce I, Renedo M, Montgomery K, Kucherlapati R, Fernández-Ruiz E. Human KLRF1, a novel member of the killer cell lectin-like receptor gene family: molecular characterization, genomic structure, physical mapping to the NK gene complex and expression analysis. European Journal of Immunology. 30: 568-76. PMID 10671213 DOI: 10.1002/1521-4141(200002)30:2<568::Aid-Immu568>3.0.Co;2-Y |
0.402 |
|
| 2000 |
Wu G, Markowitz GS, Li L, D'Agati VD, Factor SM, Geng L, Tibara S, Tuchman J, Cai Y, Park JH, van Adelsberg J, Hou H, Kucherlapati R, Edelmann W, Somlo S. Cardiac defects and renal failure in mice with targeted mutations in Pkd2. Nature Genetics. 24: 75-8. PMID 10615132 DOI: 10.1038/71724 |
0.312 |
|
| 1999 |
Heyer J, Escalante-Alcalde D, Lia M, Boettinger E, Edelmann W, Stewart CL, Kucherlapati R. Postgastrulation Smad2-deficient embryos show defects in embryo turning and anterior morphogenesis. Proceedings of the National Academy of Sciences of the United States of America. 96: 12595-600. PMID 10535967 DOI: 10.1073/Pnas.96.22.12595 |
0.305 |
|
| 1999 |
Heyer J, Yang K, Lipkin M, Edelmann W, Kucherlapati R. Mouse models for colorectal cancer. Oncogene. 18: 5325-33. PMID 10498885 DOI: 10.1038/Sj.Onc.1203036 |
0.378 |
|
| 1999 |
Murty VV, Montgomery K, Dutta S, Bala S, Renault B, Bosl GJ, Kucherlapati R, Chaganti RS. A 3-Mb high-resolution BAC/PAC contig of 12q22 encompassing the 830-kb consensus minimal deletion in male germ cell tumors. Genome Research. 9: 662-71. PMID 10413405 DOI: 10.1101/Gr.9.7.662 |
0.408 |
|
| 1999 |
Smits R, Kielman MF, Breukel C, Zurcher C, Neufeld K, Jagmohan-Changur S, Hofland N, van Dijk J, White R, Edelmann W, Kucherlapati R, Khan PM, Fodde R. Apc1638T: a mouse model delineating critical domains of the adenomatous polyposis coli protein involved in tumorigenesis and development. Genes & Development. 13: 1309-21. PMID 10346819 DOI: 10.1101/Gad.13.10.1309 |
0.332 |
|
| 1999 |
Sakuntabhai A, Ruiz-Perez V, Carter S, Jacobsen N, Burge S, Monk S, Smith M, Munro CS, O'Donovan M, Craddock N, Kucherlapati R, Rees JL, Owen M, Lathrop GM, Monaco AP, et al. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nature Genetics. 21: 271-7. PMID 10080178 DOI: 10.1038/6784 |
0.389 |
|
| 1999 |
Weiss A, McDonough D, Wertman B, Acakpo-Satchivi L, Montgomery K, Kucherlapati R, Leinwand L, Krauter K. Organization of human and mouse skeletal myosin heavy chain gene clusters is highly conserved. Proceedings of the National Academy of Sciences of the United States of America. 96: 2958-63. PMID 10077619 DOI: 10.1073/Pnas.96.6.2958 |
0.586 |
|
| 1999 |
Edelmann W, Cohen PE, Kneitz B, Winand N, Lia M, Heyer J, Kolodner R, Pollard JW, Kucherlapati R. Mammalian MutS homologue 5 is required for chromosome pairing in meiosis. Nature Genetics. 21: 123-7. PMID 9916805 DOI: 10.1038/5075 |
0.397 |
|
| 1998 |
Saint-Jore B, Puech A, Heyer J, Lin Q, Raine C, Kucherlapati R, Skoultchi AI. Goosecoid-like (Gscl), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development. Human Molecular Genetics. 7: 1841-9. PMID 9811927 DOI: 10.1093/Hmg/7.12.1841 |
0.425 |
|
| 1998 |
Ness SL, Edelmann W, Jenkins TD, Liedtke W, Rustgi AK, Kucherlapati R. Mouse keratin 4 is necessary for internal epithelial integrity. The Journal of Biological Chemistry. 273: 23904-11. PMID 9727004 DOI: 10.1074/Jbc.273.37.23904 |
0.327 |
|
| 1998 |
Kucherlapati R. Gene knockouts galore. Nature Biotechnology. 16: 519-20. PMID 9624678 DOI: 10.1038/Nbt0698-519 |
0.347 |
|
| 1998 |
Wu G, D'Agati V, Cai Y, Markowitz G, Park JH, Reynolds DM, Maeda Y, Le TC, Hou H, Kucherlapati R, Edelmann W, Somlo S. Somatic inactivation of Pkd2 results in polycystic kidney disease. Cell. 93: 177-88. PMID 9568711 DOI: 10.1016/S0092-8674(00)81570-6 |
0.312 |
|
| 1997 |
Funke B, Saint-Jore B, Puech A, Sirotkin H, Edelmann L, Carlson C, Raft S, Pandita RK, Kucherlapati R, Skoultchi A, Morrow BE. Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11. Genomics. 46: 364-72. PMID 9441739 DOI: 10.1006/Geno.1997.5046 |
0.738 |
|
| 1997 |
Puech A, Saint-Jore B, Funke B, Gilbert DJ, Sirotkin H, Copeland NG, Jenkins NA, Kucherlapati R, Morrow B, Skoultchi AI. Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization. Proceedings of the National Academy of Sciences of the United States of America. 94: 14608-13. PMID 9405660 DOI: 10.1073/Pnas.94.26.14608 |
0.753 |
|
| 1997 |
Merscher S, Marondel I, Pedeutour F, Gaudray P, Kucherlapati R, Turc-Carel C. Identification of new translocation breakpoints at 12q13 in lipomas. Genomics. 46: 70-7. PMID 9403060 DOI: 10.1006/Geno.1997.4993 |
0.432 |
|
| 1997 |
Edelmann W, Yang K, Umar A, Heyer J, Lau K, Fan K, Liedtke W, Cohen PE, Kane MF, Lipford JR, Yu N, Crouse GF, Pollard JW, Kunkel T, Lipkin M, ... ... Kucherlapati R, et al. Mutation in the mismatch repair gene Msh6 causes cancer susceptibility. Cell. 91: 467-77. PMID 9390556 DOI: 10.1016/S0092-8674(00)80433-X |
0.384 |
|
| 1997 |
Acakpo-Satchivi LJ, Edelmann W, Sartorius C, Lu BD, Wahr PA, Watkins SC, Metzger JM, Leinwand L, Kucherlapati R. Growth and muscle defects in mice lacking adult myosin heavy chain genes. The Journal of Cell Biology. 139: 1219-29. PMID 9382868 DOI: 10.1083/Jcb.139.5.1219 |
0.502 |
|
| 1997 |
Renault B, Hovnanian A, Bryce S, Chang JJ, Lau S, Sakuntabhai A, Monk S, Carter S, Ross CJ, Pang J, Twells R, Chamberlain S, Monaco AP, Strachan T, Kucherlapati R. A sequence-ready physical map of a region of 12q24.1. Genomics. 45: 271-8. PMID 9344649 DOI: 10.1006/Geno.1997.4888 |
0.411 |
|
| 1997 |
Carlson C, Sirotkin H, Pandita R, Goldberg R, McKie J, Wadey R, Patanjali SR, Weissman SM, Anyane-Yeboa K, Warburton D, Scambler P, Shprintzen R, Kucherlapati R, Morrow BE. Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients. American Journal of Human Genetics. 61: 620-9. PMID 9326327 DOI: 10.1086/515508 |
0.741 |
|
| 1997 |
Sirotkin H, Morrow B, Saint-Jore B, Puech A, Das Gupta R, Patanjali SR, Skoultchi A, Weissman SM, Kucherlapati R. Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndrome. Genomics. 42: 245-51. PMID 9192844 DOI: 10.1006/Geno.1997.4734 |
0.732 |
|
| 1997 |
Marcus DM, Rustgi AK, Defoe D, Brooks SE, McCormick RS, Thompson TP, Edelmann W, Kucherlapati R, Smith S. Retinal pigment epithelium abnormalities in mice with adenomatous polyposis coli gene disruption. Archives of Ophthalmology (Chicago, Ill. : 1960). 115: 645-50. PMID 9152133 DOI: 10.1001/Archopht.1997.01100150647013 |
0.334 |
|
| 1997 |
Sirotkin H, O'Donnell H, DasGupta R, Halford S, St Jore B, Puech A, Parimoo S, Morrow B, Skoultchi A, Weissman SM, Scambler P, Kucherlapati R. Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome. Genomics. 41: 75-83. PMID 9126485 DOI: 10.1006/Geno.1997.4627 |
0.723 |
|
| 1997 |
Yang K, Edelmann W, Fan K, Lau K, Kolli VR, Fodde R, Khan PM, Kucherlapati R, Lipkin M. A mouse model of human familial adenomatous polyposis. The Journal of Experimental Zoology. 277: 245-54. PMID 9062998 DOI: 10.1002/(Sici)1097-010X(19970215)277:3<245::Aid-Jez5>3.0.Co;2-O |
0.344 |
|
| 1997 |
Smits R, Kartheuser A, Jagmohan-Changur S, Leblanc V, Breukel C, de Vries A, van Kranen H, van Krieken JH, Williamson S, Edelmann W, Kucherlapati R, KhanPM, Fodde R. Loss of Apc and the entire chromosome 18 but absence of mutations at the Ras and Tp53 genes in intestinal tumors from Apc1638N, a mouse model for Apc-driven carcinogenesis. Carcinogenesis. 18: 321-7. PMID 9054624 DOI: 10.1093/Carcin/18.2.321 |
0.396 |
|
| 1997 |
Hamann J, Montgomery KT, Lau S, Kucherlapati R, van Lier RA. AICL: a new activation-induced antigen encoded by the human NK gene complex. Immunogenetics. 45: 295-300. PMID 9038101 DOI: 10.1007/S002510050208 |
0.374 |
|
| 1997 |
Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE. Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome. Nature Genetics. 15: 30-5. PMID 8988165 DOI: 10.1038/Ng0197-30 |
0.372 |
|
| 1996 |
Lipkin M, Yang K, Edelmann W, Newmark H, Fan KH, Risio M, Kucherlapati R. Inherited and acquired risk factors in colonic neoplasia and modulation by chemopreventive interventions. Journal of Cellular Biochemistry. Supplement. 25: 136-41. PMID 9027610 DOI: 10.1002/(Sici)1097-4644(1996)25+<136::Aid-Jcb19>3.0.Co;2-M |
0.312 |
|
| 1996 |
Cupelli L, Renault B, Leblanc-Straceski J, Banks A, Ward D, Kucherlapati RS, Krauter K. Assignment of the human myogenic factors 5 and 6 (MYF5, MYF6) gene cluster to 12q21 by in situ hybridization and physical mapping of the locus between D12S350 and D12S106. Cytogenetics and Cell Genetics. 72: 250-1. PMID 8978788 DOI: 10.1159/000134201 |
0.399 |
|
| 1996 |
Deere M, Johnson J, Garza S, Harrison WR, Yoon SJ, Elder FF, Kucherlapati R, Hook M, Hecht JT. Characterization of human DSPG3, a small dermatan sulfate proteoglycan. Genomics. 38: 399-404. PMID 8975717 DOI: 10.1006/Geno.1996.0643 |
0.38 |
|
| 1996 |
Marondel I, Renault B, Lieman J, Ward D, Kucherlapati R. Physical mapping of the human neurotensin gene (NTS) between markers D12S1444 and D12S81 on chromosome 12q21. Genomics. 38: 243-5. PMID 8954810 DOI: 10.1006/Geno.1996.0624 |
0.448 |
|
| 1996 |
Barnes KC, Neely JD, Duffy DL, Freidhoff LR, Breazeale DR, Schou C, Naidu RP, Levett PN, Renault B, Kucherlapati R, Iozzino S, Ehrlich E, Beaty TH, Marsh DG. Linkage of asthma and total serum IgE concentration to markers on chromosome 12q: evidence from Afro-Caribbean and Caucasian populations. Genomics. 37: 41-50. PMID 8921368 DOI: 10.1006/Geno.1996.0518 |
0.329 |
|
| 1996 |
Schoenberg Fejzo M, Ashar HR, Krauter KS, Powell WL, Rein MS, Weremowicz S, Yoon SJ, Kucherlapati RS, Chada K, Morton CC. Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomas. Genes, Chromosomes & Cancer. 17: 1-6. PMID 8889500 DOI: 10.1002/(Sici)1098-2264(199609)17:1<1::Aid-Gcc1>3.0.Co;2-0 |
0.431 |
|
| 1996 |
Lachman HM, Morrow B, Shprintzen R, Veit S, Parsia SS, Faedda G, Goldberg R, Kucherlapati R, Papolos DF. Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome. American Journal of Medical Genetics. 67: 468-72. PMID 8886163 DOI: 10.1002/(Sici)1096-8628(19960920)67:5<468::Aid-Ajmg5>3.0.Co;2-G |
0.358 |
|
| 1996 |
Murty VV, Renault B, Falk CT, Bosl GJ, Kucherlapati R, Chaganti RS. Physical mapping of a commonly deleted region, the site of a candidate tumor suppressor gene, at 12q22 in human male germ cell tumors. Genomics. 35: 562-70. PMID 8812492 DOI: 10.1006/Geno.1996.0398 |
0.391 |
|
| 1996 |
Sirotkin H, Morrow B, DasGupta R, Goldberg R, Patanjali SR, Shi G, Cannizzaro L, Shprintzen R, Weissman SM, Kucherlapati R. Isolation of a new clathrin heavy chain gene with muscle-specific expression from the region commonly deleted in velo-cardio-facial syndrome. Human Molecular Genetics. 5: 617-24. PMID 8733128 DOI: 10.1093/Hmg/5.5.617 |
0.71 |
|
| 1996 |
Edelmann W, Kucherlapati R. Role of recombination enzymes in mammalian cell survival. Proceedings of the National Academy of Sciences of the United States of America. 93: 6225-7. PMID 8692795 DOI: 10.1073/Pnas.93.13.6225 |
0.409 |
|
| 1996 |
Edelmann W, Cohen PE, Kane M, Lau K, Morrow B, Bennett S, Umar A, Kunkel T, Cattoretti G, Chaganti R, Pollard JW, Kolodner RD, Kucherlapati R. Meiotic pachytene arrest in MLH1-deficient mice. Cell. 85: 1125-34. PMID 8674118 DOI: 10.1016/S0092-8674(00)81312-4 |
0.359 |
|
| 1996 |
Kuefer MU, Look AT, Williams DC, Valentine V, Naeve CW, Behm FG, Mullersman JE, Yoneda-Kato N, Montgomery K, Kucherlapati R, Morris SW. cDNA cloning, tissue distribution, and chromosomal localization of myelodysplasia/myeloid leukemia factor 2 (MLF2). Genomics. 35: 392-6. PMID 8661158 DOI: 10.1006/Geno.1996.0376 |
0.448 |
|
| 1996 |
Van de Ven W, Hagemeijer A, Kucherlapati R, Marynen P. Report of the International Meeting on Chromosome 12 Genes in Cancer. Cytogenetics and Cell Genetics. 73: 25-32. PMID 8646887 DOI: 10.1159/000134309 |
0.41 |
|
| 1996 |
Marynen P, Kucherlapati R. Report of the Third International Workshop on Human Chromosome 12 Mapping 1995. Cytogenetics and Cell Genetics. 73: 1-24. PMID 8646874 DOI: 10.1159/000134308 |
0.386 |
|
| 1996 |
Johnson DW, Berg JN, Baldwin MA, Gallione CJ, Marondel I, Yoon SJ, Stenzel TT, Speer M, Pericak-Vance MA, Diamond A, Guttmacher AE, Jackson CE, Attisano L, Kucherlapati R, Porteous ME, et al. Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2. Nature Genetics. 13: 189-95. PMID 8640225 DOI: 10.1038/Ng0696-189 |
0.437 |
|
| 1996 |
Edelmann W, Zervas M, Costello P, Roback L, Fischer I, Hammarback JA, Cowan N, Davies P, Wainer B, Kucherlapati R. Neuronal abnormalities in microtubule-associated protein 1B mutant mice. Proceedings of the National Academy of Sciences of the United States of America. 93: 1270-5. PMID 8577753 DOI: 10.1073/Pnas.93.3.1270 |
0.313 |
|
| 1996 |
Morrow B, Sirotkin H, Goldberg R, Carlson C, Shprintzen R, Kucherlapati R. Association of schizophrenia with VCFS and 22q11 deletions Biological Psychiatry. 39: 540. DOI: 10.1016/0006-3223(96)84088-1 |
0.664 |
|
| 1995 |
Renault B, Lieman J, Ward D, Krauter K, Kucherlapati R. Localization of the human achaete-scute homolog gene (ASCL1) distal to phenylalanine hydroxylase (PAH) and proximal to tumor rejection antigen (TRA1) on chromosome 12q22-q23. Genomics. 30: 81-3. PMID 8595908 DOI: 10.1006/Geno.1995.0012 |
0.457 |
|
| 1995 |
Miller PL, Nadkarni PM, Kidd KK, Cheung K, Ward DC, Banks A, Bray-Ward P, Cupelli L, Herdman V, Marondel I, Montgomery K, Renault B, Yoon SJ, Krauter KS, Kucherlapati R. Internet-based support for bioscience research: a collaborative genome center for human chromosome 12. Journal of the American Medical Informatics Association : Jamia. 2: 351-64. PMID 8581551 DOI: 10.1136/Jamia.1995.96157828 |
0.363 |
|
| 1995 |
Davies RL, Yoon SJ, Weissenbach J, Ward D, Krauter K, Kucherlapati R. Physical mapping of the human ELA1 gene between D12S361 and D12S347 on chromosome 12q13. Genomics. 29: 766-8. PMID 8575772 DOI: 10.1006/Geno.1995.9939 |
0.44 |
|
| 1995 |
Umanoff H, Edelmann W, Pellicer A, Kucherlapati R. The murine N-ras gene is not essential for growth and development. Proceedings of the National Academy of Sciences of the United States of America. 92: 1709-13. PMID 7878045 DOI: 10.1073/Pnas.92.5.1709 |
0.315 |
|
| 1995 |
Lindsay EA, Goldberg R, Jurecic V, Morrow B, Carlson C, Kucherlapati RS, Shprintzen RJ, Baldini A. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions. American Journal of Medical Genetics. 57: 514-22. PMID 7677167 DOI: 10.1002/Ajmg.1320570339 |
0.378 |
|
| 1995 |
Fejzo MS, Yoon SJ, Montgomery KT, Rein MS, Weremowicz S, Krauter KS, Dorman TE, Fletcher JA, Mao JI, Moir DT, Kucherlapati RS, Morton CC. Identification of a YAC spanning the translocation breakpoints in uterine leiomyomata, pulmonary chondroid hamartoma, and lipoma: physical mapping of the 12q14-q15 breakpoint region in uterine leiomyomata Genomics. 26: 265-271. PMID 7601452 DOI: 10.1016/0888-7543(95)80210-D |
0.358 |
|
| 1995 |
Engle EC, Marondel I, Houtman WA, de Vries B, Loewenstein A, Lazar M, Ward DC, Kucherlapati R, Beggs AH. Congenital fibrosis of the extraocular muscles (autosomal dominant congenital external ophthalmoplegia): genetic homogeneity, linkage refinement, and physical mapping on chromosome 12. American Journal of Human Genetics. 57: 1086-94. PMID 7485159 |
0.324 |
|
| 1995 |
Campbell C, Marondel I, Montgomery K, Krauter K, Kucherlapati R. Unequal homologous recombination of human DNA on a yeast artificial chromosome. Nucleic Acids Research. 23: 3691-5. PMID 7478998 DOI: 10.1093/Nar/23.18.3691 |
0.361 |
|
| 1994 |
LeBlanc-Straceski JM, Montgomery KT, Kissel H, Murtaugh L, Tsai P, Ward DC, Krauter KS, Kucherlapati R. Twenty-one polymorphic markers from human chromosome 12 for integration of genetic and physical maps. Genomics. 19: 341-9. PMID 8188264 DOI: 10.1006/Geno.1994.1067 |
0.342 |
|
| 1994 |
Pedeutour F, Merscher S, Durieux E, Montgomery K, Krauter K, Clevy JP, Barcelo G, Kucherlapati R, Gaudray P, Turc-Carel C. Mapping of the 12q12-q22 region with respect to tumor translocation breakpoints. Genomics. 22: 512-8. PMID 8001964 DOI: 10.1006/Geno.1994.1424 |
0.428 |
|
| 1994 |
Kobayashi H, Montgomery KT, Bohlander SK, Adra CN, Lim BL, Kucherlapati RS, Donis-Keller H, Holt MS, Le Beau MM, Rowley JD. Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases. Blood. 84: 3473-82. PMID 7949101 DOI: 10.1182/Blood.V84.10.3473.3473 |
0.405 |
|
| 1994 |
Carter SA, Bryce SD, Munro CS, Healy E, Bashir R, Weissenbach J, LeBlanc-Straceski J, Kucherlapati R, Stephenson A, Rees JL. Linkage analyses in British pedigrees suggest a single locus for Darier disease and narrow the location to the interval between D12S105 and D12S129. Genomics. 24: 378-82. PMID 7698764 DOI: 10.1006/Geno.1994.1632 |
0.362 |
|
| 1994 |
Yoon SJ, LeBlanc-Straceski J, Ward D, Krauter K, Kucherlapati R. Organization of the human keratin type II gene cluster at 12q13. Genomics. 24: 502-8. PMID 7536183 DOI: 10.1006/Geno.1994.1659 |
0.409 |
|
| 1993 |
Das Gupta R, Morrow B, Marondel I, Parimoo S, Goei VL, Gruen J, Weissman S, Skoultchi A, Kucherlapati R. An integrated approach for identifying and mapping human genes. Proceedings of the National Academy of Sciences of the United States of America. 90: 4364-8. PMID 8506274 DOI: 10.1073/Pnas.90.10.4364 |
0.432 |
|
| 1993 |
McKusik VA, Kucherlapati RS, Ruddle FH. Genomics: stock-taking after 5 years. Genomics. 15: 1-2. PMID 8432520 DOI: 10.1006/geno.1993.1001 |
0.357 |
|
| 1993 |
Montgomery KT, LeBlanc JM, Tsai P, McNinch JS, Ward DC, de Jong PJ, Kucherlapati R, Krauter KS. Characterization of two chromosome 12 cosmid libraries and development of STSs from cosmids mapped by FISH. Genomics. 17: 682-93. PMID 8244385 DOI: 10.1006/Geno.1993.1390 |
0.423 |
|
| 1993 |
Morrow B, Kucherlapati R. Gene targeting in mammalian cells by homologous recombination. Current Opinion in Biotechnology. 4: 577-82. PMID 7764209 DOI: 10.1016/0958-1669(93)90080-G |
0.352 |
|
| 1992 |
Yoon SJ, Seiler SH, Kucherlapati R, Leinwand L. Organization of the human skeletal myosin heavy chain gene cluster. Proceedings of the National Academy of Sciences of the United States of America. 89: 12078-82. PMID 1465443 DOI: 10.1073/Pnas.89.24.12078 |
0.584 |
|
| 1991 |
Campbell C, Gulati R, Nandi AK, Floy K, Hieter P, Kucherlapati RS. Generation of a nested series of interstitial deletions in yeast artificial chromosomes carrying human DNA. Proceedings of the National Academy of Sciences of the United States of America. 88: 5744-8. PMID 2062854 DOI: 10.1073/Pnas.88.13.5744 |
0.424 |
|
| 1991 |
Schwartz F, Maeda N, Smithies O, Hickey R, Edelmann W, Skoultchi A, Kucherlapati R. A dominant positive and negative selectable gene for use in mammalian cells. Proceedings of the National Academy of Sciences of the United States of America. 88: 10416-20. PMID 1720540 DOI: 10.1073/Pnas.88.23.10416 |
0.358 |
|
| 1989 |
Kucherlapati RS. Homologous recombination in mammalian somatic cells. Progress in Nucleic Acid Research and Molecular Biology. 36: 301-10. PMID 2660192 DOI: 10.1016/S0079-6603(08)60178-6 |
0.341 |
|
| 1987 |
Kucherlapati R. Gene replacement by homologous recombination in mammalian cells. Somatic Cell and Molecular Genetics. 13: 447-9. PMID 3484087 DOI: 10.1007/Bf01534946 |
0.384 |
|
| 1987 |
Song KY, Schwartz F, Maeda N, Smithies O, Kucherlapati R. Accurate modification of a chromosomal plasmid by homologous recombination in human cells. Proceedings of the National Academy of Sciences of the United States of America. 84: 6820-4. PMID 2821545 DOI: 10.1073/Pnas.84.19.6820 |
0.45 |
|
| 1986 |
Ayares D, Chekuri L, Song KY, Kucherlapati R. Sequence homology requirements for intermolecular recombination in mammalian cells. Proceedings of the National Academy of Sciences of the United States of America. 83: 5199-203. PMID 3523485 DOI: 10.1073/Pnas.83.14.5199 |
0.393 |
|
| 1986 |
Rauth S, Song KY, Ayares D, Wallace L, Moore PD, Kucherlapati R. Transfection and homologous recombination involving single-stranded DNA substrates in mammalian cells and nuclear extracts. Proceedings of the National Academy of Sciences of the United States of America. 83: 5587-91. PMID 3461451 DOI: 10.1073/Pnas.83.15.5587 |
0.313 |
|
| 1985 |
Song KY, Chekuri L, Rauth S, Ehrlich S, Kucherlapati R. Effect of double-strand breaks on homologous recombination in mammalian cells and extracts. Molecular and Cellular Biology. 5: 3331-6. PMID 3870133 DOI: 10.1128/Mcb.5.12.3331 |
0.392 |
|
| 1985 |
Smithies O, Gregg RG, Boggs SS, Koralewski MA, Kucherlapati RS. Insertion of DNA sequences into the human chromosomal beta-globin locus by homologous recombination. Nature. 317: 230-4. PMID 2995814 DOI: 10.1038/317230A0 |
0.423 |
|
| 1985 |
Kucherlapati RS, Spencer J, Moore PD. Homologous recombination catalyzed by human cell extracts. Molecular and Cellular Biology. 5: 714-20. PMID 2985967 DOI: 10.1128/Mcb.5.4.714 |
0.353 |
|
| 1984 |
Kucherlapati RS, Eves EM, Song KY, Morse BS, Smithies O. Homologous recombination between plasmids in mammalian cells can be enhanced by treatment of input DNA. Proceedings of the National Academy of Sciences of the United States of America. 81: 3153-7. PMID 6328502 DOI: 10.1073/Pnas.81.10.3153 |
0.354 |
|
| 1984 |
Clough DW, Morse BS, Kucherlapati RS, Davidson RL. Insulin-induced reactivation of an inactive herpes simplex thymidine kinase gene. Proceedings of the National Academy of Sciences of the United States of America. 81: 838-42. PMID 6322172 DOI: 10.1073/Pnas.81.3.838 |
0.312 |
|
| 1984 |
Kucherlapati RS, Ayares D, Hanneken A, Noonan K, Rauth S, Spencer JM, Wallace L, Moore PD. Homologous recombination in monkey cells and human cell-free extracts. Cold Spring Harbor Symposia On Quantitative Biology. 49: 191-7. PMID 6099233 DOI: 10.1101/Sqb.1984.049.01.022 |
0.31 |
|
| 1984 |
Rauth S, Kucherlapati RS. Expression of DNA transferred into mammalian cells Journal of Biosciences. 6: 543-567. DOI: 10.1007/Bf02703905 |
0.362 |
|
| 1983 |
Roginski RS, Skoultchi AI, Henthorn P, Smithies O, Hsiung N, Kucherlapati R. Coordinate modulation of transfected HSV thymidine kinase and human globin genes. Cell. 35: 149-55. PMID 6313221 DOI: 10.1016/0092-8674(83)90217-9 |
0.392 |
|
| 1983 |
Hwang SP, Kucherlapati RS. Events preceding stable integration of SV40 genomes in a human cell line. Somatic Cell Genetics. 9: 457-68. PMID 6312621 DOI: 10.1007/Bf01543046 |
0.395 |
|
| 1982 |
Gilboa E, Kolbe M, Noonan K, Kucherlapati R. Construction of a mammalian transducing vector from the genome of Moloney murine leukemia virus. Journal of Virology. 44: 845-51. PMID 7176018 DOI: 10.1128/Jvi.44.3.845-851.1982 |
0.362 |
|
| 1982 |
Davies RL, Fuhrer-Krusi S, Kucherlapati RS. Modulation of transfected gene expression mediated by changes in chromatin structure. Cell. 31: 521-9. PMID 6186385 DOI: 10.1016/0092-8674(82)90308-7 |
0.346 |
|
| 1982 |
Hsiung N, Roginski RS, Henthorn P, Smithies O, Kucherlapati R, Skoultchi AI. Introduction and expression of a fetal human globin gene in mouse fibroblasts. Molecular and Cellular Biology. 2: 401-11. PMID 6180305 DOI: 10.1128/Mcb.2.4.401 |
0.384 |
|
| 1980 |
Hsiung N, Kucherlapati R. Histone gene expression and chromatin structure in mammalian cell hybrids. The Journal of Cell Biology. 87: 227-36. PMID 7419591 DOI: 10.1083/Jcb.87.1.227 |
0.361 |
|
| 1980 |
Warrick H, Hsiung N, Shows TB, Kucherlapati R. DNA-mediated cotransfer of unlinked mammalian cell markers into mouse L cells. The Journal of Cell Biology. 86: 341-6. PMID 6932400 DOI: 10.1083/Jcb.86.1.341 |
0.355 |
|
| 1980 |
Pyati J, Kucherlapati RS, Skoultchi AI. Activation of human beta-globin genes from nonerythroid cells by fusion with murine erythroleukemia cells. Proceedings of the National Academy of Sciences of the United States of America. 77: 3435-9. PMID 6932030 DOI: 10.1073/Pnas.77.6.3435 |
0.424 |
|
| 1980 |
Hsiung N, Warrick H, deRiel JK, Tuan D, Forget BG, Skoultchi A, Kucherlapati R. Cotransfer of circular and linear prokaryotic and eukaryotic DNA sequences into mouse cells. Proceedings of the National Academy of Sciences of the United States of America. 77: 4852-6. PMID 6254042 DOI: 10.1073/Pnas.77.8.4852 |
0.368 |
|
| 1980 |
Davies RL, Grosse VA, Kucherlapati R, Bothwell M. Genetic analysis of epidermal growth factor action: assignment of human epidermal growth factor receptor gene to chromosome 7. Proceedings of the National Academy of Sciences of the United States of America. 77: 4188-92. PMID 6254014 DOI: 10.1073/Pnas.77.7.4188 |
0.428 |
|
| 1980 |
Hwang SP, Kucherlapati R. Localization and organization of integrated simian virus 40 sequences in a human cell line. Virology. 105: 196-204. PMID 6251605 DOI: 10.1016/0042-6822(80)90167-1 |
0.4 |
|
| 1979 |
Kucherlapati R, Shin SI. Genetic control of tumorigenicity in interspecific mammalian cell hybrids. Cell. 16: 639-48. PMID 455444 DOI: 10.1016/0092-8674(79)90037-0 |
0.42 |
|
| 1979 |
Wolin SL, Kucherlapati RS. Expression of microtubule networks in normal cells, transformed cells, and their hybrids. The Journal of Cell Biology. 82: 76-85. PMID 383725 DOI: 10.1083/Jcb.82.1.76 |
0.334 |
|
| 1978 |
Turner BM, Smith M, Turner VS, Kucherlapati RS, Ruddle FH, Hirschhorn K. Assignment of the gene locus for human alpha-L-fucosidase to chromosome 1 by analysis of somatic cell hybrids. Somatic Cell Genetics. 4: 45-54. PMID 628884 DOI: 10.1007/Bf01546492 |
0.381 |
|
| 1978 |
Kucherlapati R, Tepper R, Granelli-Piperno A, Reich E. Modulation and mapping of a human plasminogen activator by cell fusion. Cell. 15: 1331-40. PMID 569557 DOI: 10.1016/0092-8674(78)90058-2 |
0.406 |
|
| 1978 |
Levy R, Dilley J, Sikora K, Kucherlapati R. Mouse-human hybridomas. The conversion of non-secreting human B cells into Ig secretors. Current Topics in Microbiology and Immunology. 81: 170-2. PMID 308437 DOI: 10.1007/978-3-642-67448-8_27 |
0.322 |
|
| 1978 |
Kucherlapati R, Hwang SP, Shimizu N, McDougall JK, Botchan MR. Another chromosomal assignment for a simian virus 40 integration site in human cells. Proceedings of the National Academy of Sciences of the United States of America. 75: 4460-4. PMID 212753 DOI: 10.1073/Pnas.75.9.4460 |
0.346 |
|
| 1977 |
Willecke K, Teber T, Kucherlapati RS, Ruddle FH. Human mitochondrial thymidine kinase is coded for by a gene on chromosome 16 of the nucleus. Somatic Cell Genetics. 3: 237-45. PMID 605384 DOI: 10.1007/Bf01538743 |
0.683 |
|
| 1977 |
Shimizu N, Giles RE, Kucherlapati RS, Shimizu Y, Ruddle FH. Somatic cell genetic assignment of the human gene for mitochondrial NADP-linked isocitrate dehydrogenase to the long arm of chromosome 15. Somatic Cell Genetics. 3: 47-60. PMID 564083 DOI: 10.1007/Bf01550986 |
0.607 |
|
| 1977 |
Deisseroth A, Nienhuis A, Turner P, Velez R, Anderson WF, Ruddle F, Lawrence J, Creagan R, Kucherlapati R. Localization of the human alpha-globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridization assay. Cell. 12: 205-18. PMID 561664 DOI: 10.1016/0092-8674(77)90198-2 |
0.61 |
|
| 1976 |
Shimizu N, Kucherlapati RS, Ruddle FH. Assignment of the human gene for tryptophanyl-tRNA synthetase using human-mouse somatic cell hybrids. Cytogenetics and Cell Genetics. 16: 223-6. PMID 1088821 DOI: 10.1159/000130596 |
0.584 |
|
| 1976 |
Willecke K, Reber T, Kucherlapati RS, Ruddle FH. Segregation of human mitochondrial thymidine thymidine kinase activity in human-mouse somatic cell hybrids. Birth Defects Original Article Series. 12: 252-5. PMID 1024620 |
0.6 |
|
| 1976 |
Shimizu N, Shimizu Y, Kucherlapati RS, Ruddle FH. Immunochemical detection of human enzymes in hybrid cells. Cell. 7: 123-30. PMID 985736 DOI: 10.1016/0092-8674(76)90262-2 |
0.54 |
|
| 1976 |
Anderson WF, Deisseroth AB, Velez R, Nienhuis AW, Ruddle FH, Kucherlapati RS. A new technique for mapping the human hemoglobin genes. Cytogenetics and Cell Genetics. 16: 367-71. PMID 975910 DOI: 10.1159/000130634 |
0.521 |
|
| 1976 |
Willecke K, Reber T, Kucherlapati RS, Ruddle FH. Segregation of human mitochondrial thymidine kinase activity in human-mouse somatic cell hybrids. Cytogenetics and Cell Genetics. 16: 252-5. PMID 975885 DOI: 10.1159/000130604 |
0.634 |
|
| 1976 |
Turner VS, Turner BM, Kucherlapati R, Ruddle FH, Hirschhorn K. Assignment of the human alpha-L-fucosidase gene locus to chromosome 1 by use of a "clone panel". Cytogenetics and Cell Genetics. 16: 238-40. PMID 975883 DOI: 10.1159/000130600 |
0.557 |
|
| 1976 |
Kucherlapati RS, Ruddle FH. Assignment of the human genes for mannose phosphate isomerase, pyruvate kinase (M2), and hexosaminidase-A to chromosome 15. Cytogenetics and Cell Genetics. 16: 181-3. PMID 975875 DOI: 10.1159/000130585 |
0.565 |
|
| 1976 |
Shimizu N, Kucherlapati RS, Ruddle FH. Assignment of a human gene for tryptophanyl-tRNA synthetase to chromosome 14 using human-mouse somatic cell hybrids. Somatic Cell Genetics. 2: 345-57. PMID 829178 DOI: 10.1007/Bf01538839 |
0.571 |
|
| 1976 |
Klobutcher LA, Nichols EA, Kucherlapati RS, Ruddle FH. Assignment of the gene for human adenosine kinase to chromosome 10 using a somatic cell hybrid clone panel. Birth Defects Original Article Series. 12: 171-4. PMID 192365 |
0.356 |
|
| 1976 |
McDougall JK, Gallimore PH, Dunn AR, Webb TP, Kucherlapati RS, Nichols EA, Ruddle FH. Mapping viral integration sites in somatic cell hybrids. Cytogenetics and Cell Genetics. 16: 206-10. PMID 185015 DOI: 10.1159/000130592 |
0.476 |
|
| 1976 |
Klobutcher LA, Nichols EA, Kucherlapati RS, Ruddle FH. Assignment of the gene for human adenosine kinase to chromosome 10 using a somatic cell hybrid clone panel. Cytogenetics and Cell Genetics. 16: 171-4. PMID 185014 DOI: 10.1159/000130582 |
0.603 |
|
| 1976 |
Satlin A, Kucherlapati R, Ruddle FH. Assignment of the gene for human uridine monophosphate kinase to chromosome 1 using somatic cell hybrid clone panels. Cytogenetics and Cell Genetics. 15: 146-52. PMID 172293 DOI: 10.1159/000130513 |
0.606 |
|
| 1976 |
McDougall JK, Elsevier SM, Kucherlapati RS, Ruddle FH. Regional localization of human genes in virus-induced uncoiler regions. Cytogenetics and Cell Genetics. 14: 372-4. PMID 172292 DOI: 10.1159/000130388 |
0.513 |
|
| 1976 |
Faber HE, Kucherlapati RS, Poulik MD, Ruddle FH, Smithies O. beta2-microglobulin locus on human chromosome 15. Somatic Cell Genetics. 2: 141-53. PMID 69326 DOI: 10.1007/Bf01542627 |
0.574 |
|
| 1976 |
Schacter B, Kucherlapati RS, Ruddle FH. Synteny of the loci for beta2-microglobulin and PKM2 in man-mouse somatic cell hybrid subclones. Cytogenetics and Cell Genetics. 16: 215-8. PMID 61838 DOI: 10.1159/000130594 |
0.502 |
|
| 1976 |
Kucherlapati RS, Faber HE, Poulik MD, Ruddle FH, Smithies O. Assignment of the gene for beta-2-microglobulin to human chromosome 15. Cytogenetics and Cell Genetics. 16: 178-80. PMID 61837 DOI: 10.1159/000130584 |
0.568 |
|
| 1976 |
Friend KK, Dorman BP, Kucherlapati RS, Ruddle FH. Detection of interspecific translocations in mouse-human hybrids by alkaline Giemsa staining. Experimental Cell Research. 99: 31-6. PMID 57063 DOI: 10.1016/0014-4827(76)90676-5 |
0.581 |
|
| 1975 |
Kucherlapati RS, Creagan RP, Nichols EA, Borgaonkar DS, Ruddle FH. Synteny relationships of four human genes: mannose phosphate isomerase to pyruvate kinase-3 and triose phophate isomerase to lactate dehydrogenase-B. Cytogenetics and Cell Genetics. 14: 364-7. PMID 1192819 DOI: 10.1159/000130385 |
0.333 |
|
| 1975 |
Kucherlapati RS, Baker RM, Ruddle FH. Ouabain as a selective agent in the isolation of somatic cell hybrids. Cytogenetics and Cell Genetics. 14: 362-3. PMID 1192818 DOI: 10.1159/000130384 |
0.472 |
|
| 1975 |
Kucherlapati RS, Ruddle FH. Mammalian somatic hybrids and human gene mapping. Annals of Internal Medicine. 83: 553-60. PMID 1101764 DOI: 10.7326/0003-4819-83-4-553 |
0.61 |
|
| 1975 |
Gilbert F, Kucherlapati R, Creagan RP, Murnane MJ, Darlington GJ, Ruddle FH. Tay-Sachs' and Sandhoff's diseases: the assignment of genes for hexosaminidase A and B to individual human chromosomes. Proceedings of the National Academy of Sciences of the United States of America. 72: 263-7. PMID 1054503 DOI: 10.1073/Pnas.72.1.263 |
0.58 |
|
| 1975 |
Elsevier SM, Kucherlapati RS, Nichols EA, Willecke K, Creagan RP, Giles RE, McDougall JK, Ruddle FH. Assigment and regional localization of a gene coding for galactokinase to human chromosome 17q21-22. Cytogenetics and Cell Genetics. 14: 287-9. PMID 172290 DOI: 10.1159/000130365 |
0.673 |
|
| 1975 |
Kucherlapati RS, Hilwig I, Gropp A, Ruddle FH. Mammalian chromosome identification in interspecific hybride cells using "Hoechst 33258". Human Genetics. 27: 9-14. DOI: 10.1007/Bf00283498 |
0.439 |
|
| 1974 |
Ruddle FH, Kucherlapati RS. Hybrid cells and human genes. Scientific American. 231: 36-44. PMID 4846961 DOI: 10.1038/Scientificamerican0774-36 |
0.58 |
|
| 1974 |
Gilbert F, Kucherlapati R, Murnane MJ, Darlington GJ, Creagan R, Ruddle FH. Proceedings: Assignment of a locus involved in the expression of hexosaminidase A to chromosome 7 in man. Cytogenetics and Cell Genetics. 13: 96-6. PMID 4827504 DOI: 10.1159/000130245 |
0.4 |
|
| 1974 |
Gilbert F, Kucherlapati R, Creagan R, Murnane MJ, Darlington GJ, Ruddle FH. Proceedings: Hexosaminidase B: assignment of a locus involved in its expression to chromosome 5 in man. Cytogenetics and Cell Genetics. 13: 93-5. PMID 4827503 DOI: 10.1159/000130244 |
0.537 |
|
| 1974 |
Creagan RP, Carritt B, Chen S, Kucherlapati R, McMorris FA, Ricciuti F, Tan YH, Tischfield JA, Ruddle FH. Proceedings: Confirmation of the synteny of the human genes for cytoplasmic isocitrate dehydrogenase and cytoplasmic malate dehydrogenase and assignment to chromosome 2. Cytogenetics and Cell Genetics. 13: 79-82. PMID 4827500 DOI: 10.1159/000130239 |
0.756 |
|
| 1974 |
Kucherlapati R, McDougall JK, Ruddle FH. Proceedings: Regional localization of the human genes for thymidine kinase, lactate dehydrogenase-A, and esterase-A. Cytogenetics and Cell Genetics. 13: 108-10. PMID 4827473 DOI: 10.1159/000130249 |
0.53 |
|
| 1974 |
Elsevier SM, Kucherlapati RS, Nichols EA, Creagan RP, Giles RE, Ruddle FH, Willecke K, McDougall JK. Assignment of the gene for galactokinase to human chromosome 17 and its regional localisation to band q21-22. Nature. 251: 633-6. PMID 4371022 DOI: 10.1038/251633A0 |
0.703 |
|
| 1974 |
Gilbert F, Kucherlapati R, Murnane MJ, Darlington GJ, Creagan R, Ruddle FH. Assignment of a locus involved in the expression of hexosaminidase a to chromosome 7 in man Cytogenetic and Genome Research. 13: 96-99. DOI: 10.1159/000130245 |
0.501 |
|
| 1973 |
McDougall JK, Kucherlapati R, Ruddle FH. Localization and induction of the human thymidine kinase gene by adenovirus 12. Nature: New Biology. 245: 172-5. PMID 4126392 DOI: 10.1038/Newbio245172A0 |
0.61 |
|
| Show low-probability matches. |
