| Year |
Citation |
Score |
| 2023 |
Choo ZN, Behr JM, Deshpande A, Hadi K, Yao X, Tian H, Takai K, Zakusilo G, Rosiene J, Da Cruz Paula A, Weigelt B, Setton J, Riaz N, Powell SN, Busam K, et al. Most large structural variants in cancer genomes can be detected without long reads. Nature Genetics. PMID 37945902 DOI: 10.1038/s41588-023-01540-6 |
0.301 |
|
| 2023 |
Maura F, Ziccheddu B, Xiang JZ, Bhinder B, Rosiene J, Abascal F, Maclachlan KH, Eng KW, Uppal M, He F, Zhang W, Gao Q, Yellapantula VD, Trujillo-Alonso V, Park SI, ... ... Imielinski M, et al. Molecular evolution of classic Hodgkin lymphoma revealed through whole genome sequencing of Hodgkin and Reed Sternberg cells. Blood Cancer Discovery. PMID 36723991 DOI: 10.1158/2643-3230.BCD-22-0128 |
0.301 |
|
| 2022 |
Gajic ZZ, Deshpande A, Legut M, Imieliński M, Sanjana NE. Recurrent somatic mutations as predictors of immunotherapy response. Nature Communications. 13: 3938. PMID 35803911 DOI: 10.1038/s41467-022-31055-3 |
0.313 |
|
| 2022 |
Paulson TG, Galipeau PC, Oman KM, Sanchez CA, Kuhner MK, Smith LP, Hadi K, Shah M, Arora K, Shelton J, Johnson M, Corvelo A, Maley CC, Yao X, Sanghvi R, ... ... Imielinski M, et al. Somatic whole genome dynamics of precancer in Barrett's esophagus reveals features associated with disease progression. Nature Communications. 13: 2300. PMID 35484108 DOI: 10.1038/s41467-022-29767-7 |
0.343 |
|
| 2021 |
Choi J, Manzano A, Dong W, Bellone S, Bonazzoli E, Zammataro L, Yao X, Deshpande A, Zaidi S, Guglielmi A, Gnutti B, Nagarkatti N, Tymon-Rosario JR, Harold J, Mauricio D, ... ... Imielinski M, et al. Integrated mutational landscape analysis of uterine leiomyosarcomas. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 33876771 DOI: 10.1073/pnas.2025182118 |
0.33 |
|
| 2021 |
Dentro SC, Leshchiner I, Haase K, Tarabichi M, Wintersinger J, Deshwar AG, Yu K, Rubanova Y, Macintyre G, Demeulemeester J, Vázquez-García I, Kleinheinz K, Livitz DG, Malikic S, Donmez N, ... ... Imielinski M, et al. Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes. Cell. PMID 33831375 DOI: 10.1016/j.cell.2021.03.009 |
0.371 |
|
| 2021 |
Carrot-Zhang J, Yao X, Devarakonda S, Deshpande A, Damrauer JS, Silva TC, Wong CK, Choi HY, Felau I, Robertson AG, Castro MAA, Bao L, Rheinbay E, Liu EM, Trieu T, ... ... Imielinski M, et al. Whole-genome characterization of lung adenocarcinomas lacking the RTK/RAS/RAF pathway. Cell Reports. 34: 108707. PMID 33535033 DOI: 10.1016/j.celrep.2021.108707 |
0.344 |
|
| 2020 |
Rheinbay E, Nielsen MM, Abascal F, Wala JA, Shapira O, Tiao G, Hornshøj H, Hess JM, Juul RI, Lin Z, Feuerbach L, Sabarinathan R, Madsen T, Kim J, Mularoni L, ... ... Imielinski M, et al. Analyses of non-coding somatic drivers in 2,658 cancer whole genomes. Nature. 578: 102-111. PMID 32025015 DOI: 10.1038/s41586-020-1965-x |
0.376 |
|
| 2020 |
Gerstung M, Jolly C, Leshchiner I, Dentro SC, Gonzalez S, Rosebrock D, Mitchell TJ, Rubanova Y, Anur P, Yu K, Tarabichi M, Deshwar A, Wintersinger J, Kleinheinz K, Vázquez-García I, ... ... Imielinski M, et al. The evolutionary history of 2,658 cancers. Nature. 578: 122-128. PMID 32025013 DOI: 10.1038/S41586-019-1907-7 |
0.475 |
|
| 2020 |
Li Y, Roberts ND, Wala JA, Shapira O, Schumacher SE, Kumar K, Khurana E, Waszak S, Korbel JO, Haber JE, Imielinski M, Weischenfeldt J, Beroukhim R, Campbell PJ, et al. Patterns of somatic structural variation in human cancer genomes. Nature. 578: 112-121. PMID 32025012 DOI: 10.1038/S41586-019-1913-9 |
0.425 |
|
| 2019 |
Ghandi M, Huang FW, Jané-Valbuena J, Kryukov GV, Lo CC, McDonald ER, Barretina J, Gelfand ET, Bielski CM, Li H, Hu K, Andreev-Drakhlin AY, Kim J, Hess JM, Haas BJ, ... ... Imielinski M, et al. Next-generation characterization of the Cancer Cell Line Encyclopedia. Nature. PMID 31068700 DOI: 10.1038/S41586-019-1186-3 |
0.36 |
|
| 2019 |
Gyan KE, Deshpande A, Beg S, Tian H, Rosiene J, Stoeckius M, Smibert P, Risso D, Mosquera JM, Imielinski M. Abstract 909: Single-cell transcriptomic profiling of non-small cell lung cancer uncovers inter- and intracell population structure across TCGA lung adenocarcinoma and lung squamous cancer subtypes Cancer Research. 79: 909-909. DOI: 10.1158/1538-7445.Am2019-909 |
0.4 |
|
| 2018 |
Wala JA, Bandopadhayay P, Greenwald N, O'Rourke R, Sharpe T, Stewart C, Schumacher S, Li Y, Weischenfeldt J, Yao X, Nusbaum C, Campbell P, Getz G, Meyerson M, Zhang CZ, ... Imielinski M, et al. SvABA: genome-wide detection of structural variants and indels by local assembly. Genome Research. PMID 29535149 DOI: 10.1101/Gr.221028.117 |
0.389 |
|
| 2018 |
Bakhoum SF, Ngo B, Bakhoum AL, Cavallo J, Murphy CJ, Ly P, Shah P, Sriram RK, Watkins TBk, Taunk NK, Duran M, Pauli C, Shaw C, Chadalavada K, Rajasekhar VK, ... ... Imielinski M, et al. Abstract NG03: Chromosomal instability promotes metastasis through a cytosolic DNA response Cancer Research. 78. DOI: 10.1158/1538-7445.Am2018-Ng03 |
0.338 |
|
| 2018 |
Dentro S, Leshchiner I, Haase K, Wintersinger J, Deshwar A, Tarabichi M, Rubanova Y, Yu K, García IV, Macintyre G, Kleinheinz K, Livitz D, Malikic S, Donmez N, Sengupta S, ... ... Imielinski M, et al. Abstract 3000: Pervasive intra-tumour heterogeneity and subclonal selection across cancer types Cancer Research. 78: 3000-3000. DOI: 10.1158/1538-7445.Am2018-3000 |
0.465 |
|
| 2018 |
Jolly C, Gerstung M, Leshchiner I, Dentro SC, Gonzalez S, Mitchell TJ, Rubanova Y, Anur P, Rosebrock D, Yu K, Tarabichi M, Deshwar A, Wintersinger J, Kleinheinz K, Vásquez-García I, ... ... Imielinski M, et al. Abstract 218: The evolutionary history of 2,658 cancers Cancer Research. 78: 218-218. DOI: 10.1158/1538-7445.Am2018-218 |
0.441 |
|
| 2017 |
Khosravi P, Kazemi E, Imielinski M, Elemento O, Hajirasouliha I. Deep Convolutional Neural Networks Enable Discrimination of Heterogeneous Digital Pathology Images. Ebiomedicine. PMID 29292031 DOI: 10.1016/J.Ebiom.2017.12.026 |
0.32 |
|
| 2017 |
Berger AH, Brooks AN, Wu X, Shrestha Y, Chouinard C, Piccioni F, Bagul M, Kamburov A, Imielinski M, Hogstrom L, Zhu C, Yang X, Pantel S, Sakai R, Watson J, et al. High-throughput Phenotyping of Lung Cancer Somatic Mutations. Cancer Cell. 32: 884. PMID 29232558 DOI: 10.1016/j.ccell.2017.11.008 |
0.323 |
|
| 2017 |
Maciejowski J, Imielinski M. Modeling cancer rearrangement landscapes. Current Opinion in Systems Biology. 1: 54-61. PMID 29177203 DOI: 10.1016/J.Coisb.2016.12.005 |
0.43 |
|
| 2017 |
Imielinski M, Rubin MA. Prostate cancer: Clinical hallmarks in whole cancer genomes. Nature Reviews. Clinical Oncology. PMID 28374788 DOI: 10.1038/Nrclinonc.2017.45 |
0.347 |
|
| 2017 |
Imielinski M, Guo G, Meyerson M. Insertions and Deletions Target Lineage-Defining Genes in Human Cancers. Cell. PMID 28089356 DOI: 10.1016/J.Cell.2016.12.025 |
0.43 |
|
| 2016 |
Huang L, Fernandes H, Zia H, Tavassoli P, Rennert H, Pisapia D, Imielinski M, Sboner A, Rubin MA, Kluk M, Elemento O. The cancer precision medicine knowledge base for structured clinical-grade mutations and interpretations. Journal of the American Medical Informatics Association : Jamia. PMID 27789569 DOI: 10.1093/Jamia/Ocw148 |
0.354 |
|
| 2016 |
Berger AH, Brooks AN, Wu X, Shrestha Y, Chouinard C, Piccioni F, Bagul M, Kamburov A, Imielinski M, Hogstrom L, Zhu C, Yang X, Pantel S, Sakai R, Watson J, et al. High-throughput Phenotyping of Lung Cancer Somatic Mutations. Cancer Cell. PMID 27478040 DOI: 10.1016/J.Ccell.2016.06.022 |
0.463 |
|
| 2016 |
Campbell JD, Alexandrov A, Kim J, Wala J, Berger AH, Pedamallu CS, Shukla SA, Guo G, Brooks AN, Murray BA, Imielinski M, Hu X, Ling S, Akbani R, Rosenberg M, et al. Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas. Nature Genetics. PMID 27158780 DOI: 10.1038/Ng.3564 |
0.327 |
|
| 2016 |
Berger AH, Brooks AN, Wu X, Shrestha Y, Chouinard C, Piccioni F, Bagul M, Kamburov A, Imielinski M, Hogstrom L, Zhu C, Yang X, Pantel S, Sakai R, Kaplan N, et al. Abstract 4368: High-throughput phenotyping of lung cancer somatic mutations Cancer Research. 76: 4368-4368. DOI: 10.1158/1538-7445.Am2016-4368 |
0.485 |
|
| 2015 |
Zhang X, Choi PS, Francis JM, Imielinski M, Watanabe H, Cherniack AD, Meyerson M. Identification of focally amplified lineage-specific super-enhancers in human epithelial cancers. Nature Genetics. PMID 26656844 DOI: 10.1038/Ng.3470 |
0.441 |
|
| 2014 |
Sharifnia T, Rusu V, Piccioni F, Bagul M, Imielinski M, Cherniack AD, Pedamallu CS, Wong B, Wilson FH, Garraway LA, Altshuler D, Golub TR, Root DE, Subramanian A, Meyerson M. Genetic modifiers of EGFR dependence in non-small cell lung cancer. Proceedings of the National Academy of Sciences of the United States of America. 111: 18661-6. PMID 25512530 DOI: 10.1073/Pnas.1412228112 |
0.357 |
|
| 2014 |
Imielinski M, Greulich H, Kaplan B, Araujo L, Amann J, Horn L, Schiller J, Villalona-Calero MA, Meyerson M, Carbone DP. Oncogenic and sorafenib-sensitive ARAF mutations in lung adenocarcinoma. The Journal of Clinical Investigation. 124: 1582-6. PMID 24569458 DOI: 10.1172/Jci72763 |
0.451 |
|
| 2014 |
Brooks AN, Choi PS, de Waal L, Sharifnia T, Imielinski M, Saksena G, Pedamallu CS, Sivachenko A, Rosenberg M, Chmielecki J, Lawrence MS, DeLuca DS, Getz G, Meyerson M. A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing events. Plos One. 9: e87361. PMID 24498085 DOI: 10.1371/Journal.Pone.0087361 |
0.463 |
|
| 2014 |
Berger AH, Imielinski M, Duke F, Wala J, Kaplan N, Shi GX, Andres DA, Meyerson M. Oncogenic RIT1 mutations in lung adenocarcinoma. Oncogene. 33: 4418-23. PMID 24469055 DOI: 10.1038/onc.2013.581 |
0.302 |
|
| 2014 |
Berger AH, Brooks AN, Imielinski M, Cherniack A, Duke F, Kaplan N, Wala J, Meyerson M. Abstract PR08:NF1,MET, andRIT1mutations are RAS-pathway driver events in lung adenocarcinoma Molecular Cancer Research. 12. DOI: 10.1158/1557-3125.Rasonc14-Pr08 |
0.44 |
|
| 2014 |
Imielinski M, Du C, Meyerson M. Abstract 4263: Identifying somatic mutation hotspots across protein family alignments Cancer Research. 74: 4263-4263. DOI: 10.1158/1538-7445.Am2014-4263 |
0.389 |
|
| 2013 |
Alexandrov LB, Nik-Zainal S, Wedge DC, Aparicio SA, Behjati S, Biankin AV, Bignell GR, Bolli N, Borg A, Børresen-Dale AL, Boyault S, Burkhardt B, Butler AP, Caldas C, Davies HR, ... ... Imielinski M, et al. Signatures of mutational processes in human cancer. Nature. 500: 415-21. PMID 23945592 DOI: 10.1038/Nature12477 |
0.354 |
|
| 2013 |
Lawrence MS, Stojanov P, Polak P, Kryukov GV, Cibulskis K, Sivachenko A, Carter SL, Stewart C, Mermel CH, Roberts SA, Kiezun A, Hammerman PS, McKenna A, Drier Y, Zou L, ... ... Imielinski M, et al. Mutational heterogeneity in cancer and the search for new cancer-associated genes. Nature. 499: 214-8. PMID 23770567 DOI: 10.1038/Nature12213 |
0.475 |
|
| 2013 |
Brooks AN, Wan Y, Choi P, Jing R, DeLuca DS, Sougnez C, Chmielecki J, Imielinski M, Getz G, Wu CJ, Meyerson M. Abstract 3150: Characterizing the effects of somatic mutations in splice factors on the transcriptome. Cancer Research. 73: 3150-3150. DOI: 10.1158/1538-7445.Am2013-3150 |
0.337 |
|
| 2013 |
Chmielecki J, Rosenberg M, Imielinski M, Hernandez B, Lawrence M, Sivachenko A, Cibulskis K, Voet D, Sougnez C, Gabriel S, Getz G, Meyerson M. Abstract 1112: Whole exome and whole genome sequence analysis of lung adenocarcinoma. Cancer Research. 73: 1112-1112. DOI: 10.1158/1538-7445.Am2013-1112 |
0.506 |
|
| 2013 |
Berger A, Imielinski M, Duke F, Wala J, Kaplan N, Shi G, Andres D, Meyerson M. Abstract C140: RIT1 mutations define a new genetic subset of lung adenocarcinoma. Molecular Cancer Therapeutics. 12. DOI: 10.1158/1535-7163.Targ-13-C140 |
0.438 |
|
| 2013 |
Greulich HE, Imielinski M, Kaplan B, Araujo L, Amann J, Horn L, Villalona M, Meyerson M, Carbone D. Abstract C139: Oncogenic ARAF mutation in a metastatic lung adenocarcinoma from a patient exhibiting sustained sorafenib response. Molecular Cancer Therapeutics. 12. DOI: 10.1158/1535-7163.Targ-13-C139 |
0.448 |
|
| 2013 |
Imielinski M, Du C, Meyerson M. Abstract A22: Identifying somatic mutation hotspots across protein family alignments. Molecular Cancer Therapeutics. 12. DOI: 10.1158/1535-7163.Targ-13-A22 |
0.387 |
|
| 2013 |
Alexandrov LB, Nik-Zainal S, Wedge DC, Aparicio SAJR, Behjati S, Biankin AV, Bignell GR, Bolli N, Borg A, Børresen-Dale A, Boyault S, Burkhardt B, Butler AP, Caldas C, Davies HR, ... ... Imielinski M, et al. Corrigendum: Signatures of mutational processes in human cancer Nature. 502: 258-258. DOI: 10.1038/Nature12666 |
0.334 |
|
| 2012 |
Imielinski M, Berger AH, Hammerman PS, Hernandez B, Pugh TJ, Hodis E, Cho J, Suh J, Capelletti M, Sivachenko A, Sougnez C, Auclair D, Lawrence MS, Stojanov P, Cibulskis K, et al. Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing. Cell. 150: 1107-20. PMID 22980975 DOI: 10.1016/J.Cell.2012.08.029 |
0.452 |
|
| 2012 |
Hammerman PS, Voet D, Lawrence MS, Jing R, Cibulskis K, Sivachenko A, Stojanov P, McKenna A, Lander ES, Gabriel S, Getz G, Imielinski M, Helman E, Hernandez B, Pho NH, et al. Comprehensive genomic characterization of squamous cell lung cancers Nature. 489: 519-525. PMID 22960745 DOI: 10.1038/Nature11404 |
0.476 |
|
| 2012 |
Greulich H, Kaplan B, Mertins P, Chen TH, Tanaka KE, Yun CH, Zhang X, Lee SH, Cho J, Ambrogio L, Liao R, Imielinski M, Banerji S, Berger AH, Lawrence MS, et al. Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2. Proceedings of the National Academy of Sciences of the United States of America. 109: 14476-81. PMID 22908275 DOI: 10.1073/Pnas.1203201109 |
0.369 |
|
| 2012 |
Hodis E, Watson IR, Kryukov GV, Arold ST, Imielinski M, Theurillat JP, Nickerson E, Auclair D, Li L, Place C, Dicara D, Ramos AH, Lawrence MS, Cibulskis K, Sivachenko A, et al. A landscape of driver mutations in melanoma. Cell. 150: 251-63. PMID 22817889 DOI: 10.1016/J.Cell.2012.06.024 |
0.406 |
|
| 2012 |
Imielinski M, Cha S, Rejtar T, Richardson EA, Karger BL, Sgroi DC. Integrated proteomic, transcriptomic, and biological network analysis of breast carcinoma reveals molecular features of tumorigenesis and clinical relapse. Molecular & Cellular Proteomics : McP. 11: M111.014910. PMID 22240506 DOI: 10.1074/Mcp.M111.014910 |
0.33 |
|
| 2012 |
Elia J, Glessner JT, Wang K, Takahashi N, Shtir CJ, Hadley D, Sleiman PM, Zhang H, Kim CE, Robison R, Lyon GJ, Flory JH, Bradfield JP, Imielinski M, Hou C, et al. Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature Genetics. 44: 78-84. PMID 22138692 DOI: 10.1038/Ng.1013 |
0.342 |
|
| 2012 |
Imielinski M, Hernandez B, Lawrence M, Hodis E, Kryukov G, Stojanov P, Sivachenko A, Cibulskis K, Sougnez C, Auclair D, Ardlie K, Banerji S, Hammerman P, Thomas RK, Gabriel S, et al. Abstract 1682: Uncovering signals of somatic selection through whole exome and whole genome sequencing of lung adenocarcinoma Cancer Research. 72: 1682-1682. DOI: 10.1158/1538-7445.Am2012-1682 |
0.482 |
|
| 2012 |
Greulich H, Kaplan B, Mertins P, Chen T, Tanaka K, Yun C, Imielinski M, Banerji S, Lawrence MS, Walker S, Winckler W, Getz G, Frank D, Eck M, Jaffe JD, et al. Abstract 1: Oncogenic extracellular domain mutations of ERBB2 in cancer Cancer Research. 72: 1-1. DOI: 10.1158/1538-7445.Am2012-1 |
0.363 |
|
| 2012 |
Hernandez B, Hammerman P, Imielinski M, Lawrence M, Stojanov P, Getz G, Meyerson M. Abstract PR1: Integrating expression data improves mutational significance analysis of lung squamous carcinoma Clinical Cancer Research. 18. DOI: 10.1158/1078-0432.12Aacriaslc-Pr1 |
0.476 |
|
| 2011 |
Bradfield JP, Qu HQ, Wang K, Zhang H, Sleiman PM, Kim CE, Mentch FD, Qiu H, Glessner JT, Thomas KA, Frackelton EC, Chiavacci RM, Imielinski M, Monos DS, Pandey R, et al. A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. Plos Genetics. 7: e1002293. PMID 21980299 DOI: 10.1371/Journal.Pgen.1002293 |
0.379 |
|
| 2011 |
Bell D, Berchuck A, Birrer M, Chien J, Cramer DW, Dao F, Dhir R, Disaia P, Gabra H, Glenn P, Godwin AK, Gross J, Hartmann L, Huang M, Huntsman DG, ... ... Imielinski M, et al. Integrated genomic analyses of ovarian carcinoma Nature. 474: 609-615. PMID 21720365 DOI: 10.1038/Nature10166 |
0.416 |
|
| 2011 |
Anderson CA, Boucher G, Lees CW, Franke A, D'Amato M, Taylor KD, Lee JC, Goyette P, Imielinski M, Latiano A, Lagacé C, Scott R, Amininejad L, Bumpstead S, Baidoo L, et al. Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Nature Genetics. 43: 246-52. PMID 21297633 DOI: 10.1038/Ng.764 |
0.376 |
|
| 2010 |
Glessner JT, Wang K, Sleiman PM, Zhang H, Kim CE, Flory JH, Bradfield JP, Imielinski M, Frackelton EC, Qiu H, Mentch F, Grant SF, Hakonarson H. Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder. Plos One. 5: e15463. PMID 21152026 DOI: 10.1371/Journal.Pone.0015463 |
0.331 |
|
| 2010 |
Imielinski M, Belta C. Deep epistasis in human metabolism. Chaos (Woodbury, N.Y.). 20: 026104. PMID 20590333 DOI: 10.1063/1.3456056 |
0.319 |
|
| 2010 |
Imielinski M, Hakonarson H. Breaking new ground in inflammatory bowel disease genetics: genome-wide association studies and beyond. Pharmacogenomics. 11: 663-5. PMID 20415557 DOI: 10.2217/Pgs.10.56 |
0.329 |
|
| 2010 |
Wang K, Baldassano R, Zhang H, Qu HQ, Imielinski M, Kugathasan S, Annese V, Dubinsky M, Rotter JI, Russell RK, Bradfield JP, Sleiman PM, Glessner JT, Walters T, Hou C, et al. Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects. Human Molecular Genetics. 19: 2059-67. PMID 20176734 DOI: 10.1093/Hmg/Ddq078 |
0.304 |
|
| 2009 |
Grant SF, Petri M, Bradfield JP, Kim CE, Santa E, Annaiah K, Frackelton EC, Glessner JT, Otieno FG, Shaner JL, Smith RM, Eckert AW, Chiavacci RM, Imielinski M, Sullivan KE, et al. Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry. The Application of Clinical Genetics. 2: 1-5. PMID 23776345 DOI: 10.2147/Tacg.S4089 |
0.323 |
|
| 2009 |
Imielinski M, Baldassano RN, Griffiths A, Russell RK, Annese V, Dubinsky M, Kugathasan S, Bradfield JP, Walters TD, Sleiman P, Kim CE, Muise A, Wang K, Glessner JT, Saeed S, et al. Common variants at five new loci associated with early-onset inflammatory bowel disease. Nature Genetics. 41: 1335-40. PMID 19915574 DOI: 10.1038/Ng.489 |
0.309 |
|
| 2009 |
Shaikh TH, Gai X, Perin JC, Glessner JT, Xie H, Murphy K, O'Hara R, Casalunovo T, Conlin LK, D'Arcy M, Frackelton EC, Geiger EA, Haldeman-Englert C, Imielinski M, Kim CE, et al. High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. Genome Research. 19: 1682-90. PMID 19592680 DOI: 10.1101/Gr.083501.108 |
0.379 |
|
| 2009 |
Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, et al. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. Plos Genetics. 5: e1000536. PMID 19557195 DOI: 10.1371/Journal.Pgen.1000536 |
0.391 |
|
| 2009 |
Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature. 459: 569-73. PMID 19404257 DOI: 10.1038/Nature07953 |
0.385 |
|
| 2009 |
Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 459: 528-33. PMID 19404256 DOI: 10.1038/Nature07999 |
0.345 |
|
| 2009 |
Wang K, Zhang H, Kugathasan S, Annese V, Bradfield JP, Russell RK, Sleiman PM, Imielinski M, Glessner J, Hou C, Wilson DC, Walters T, Kim C, Frackelton EC, Lionetti P, et al. Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease. American Journal of Human Genetics. 84: 399-405. PMID 19249008 DOI: 10.1016/J.Ajhg.2009.01.026 |
0.384 |
|
| 2009 |
Grant SF, Qu HQ, Bradfield JP, Marchand L, Kim CE, Glessner JT, Grabs R, Taback SP, Frackelton EC, Eckert AW, Annaiah K, Lawson ML, Otieno FG, Santa E, Shaner JL, ... ... Imielinski M, et al. Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. Diabetes. 58: 290-5. PMID 18840781 DOI: 10.2337/Db08-1022 |
0.321 |
|
| 2008 |
Kugathasan S, Baldassano RN, Bradfield JP, Sleiman PM, Imielinski M, Guthery SL, Cucchiara S, Kim CE, Frackelton EC, Annaiah K, Glessner JT, Santa E, Willson T, Eckert AW, Bonkowski E, et al. Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. Nature Genetics. 40: 1211-5. PMID 18758464 DOI: 10.1038/Ng.203 |
0.327 |
|
| 2008 |
Imielinski M, Belta C. Exploiting the pathway structure of metabolism to reveal high-order epistasis. Bmc Systems Biology. 2: 40. PMID 18447928 DOI: 10.1186/1752-0509-2-40 |
0.321 |
|
| 2008 |
Grant SF, Li M, Bradfield JP, Kim CE, Annaiah K, Santa E, Glessner JT, Casalunovo T, Frackelton EC, Otieno FG, Shaner JL, Smith RM, Imielinski M, Eckert AW, Chiavacci RM, et al. Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP. Plos One. 3: e1746. PMID 18335027 DOI: 10.1371/Journal.Pone.0001746 |
0.302 |
|
| 2006 |
Imielinski M, Belta C, Rubin H, Halász A. Systematic analysis of conservation relations in Escherichia coli genome-scale metabolic network reveals novel growth media. Biophysical Journal. 90: 2659-72. PMID 16461408 DOI: 10.1529/Biophysj.105.069278 |
0.48 |
|
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