Raju S Kucherlapati - Publications

Affiliations: 
Harvard Medical School, Boston, MA, United States 
Area:
genetics
Website:
https://xconomy.com/author/rkucherlapati/

227 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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  0.316
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  0.351
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  0.337
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  0.393
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  0.356
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  0.613
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  0.312
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  0.346
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  0.336
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  0.355
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  0.394
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  0.746
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  0.39
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  0.367
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  0.421
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  0.424
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  0.735
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  0.751
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  0.431
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  0.738
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  0.729
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  0.72
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  0.357
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  0.706
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  0.385
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  0.66
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  0.377
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  0.357
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  0.323
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  0.427
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  0.345
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  0.564
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  0.609
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  0.399
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  0.755
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  0.5
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
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