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Deanna M. Church - Publications

Affiliations: 
National Center for Biotechnology Information, National Library of Medicine National Institutes of Health, Bethesda, MD 
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78 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
2022 Mohr DW, Gaughran SJ, Paschall J, Naguib A, Pang AWC, Dudchenko O, Aiden EL, Church DM, Scott AF. A Chromosome-Length Assembly of the Hawaiian Monk Seal (): A History of "Genetic Purging" and Genomic Stability. Genes. 13. PMID 35886053 DOI: 10.3390/genes13071270  0.303
2022 Church DM. A next-generation human genome sequence. Science (New York, N.Y.). 376: 34-35. PMID 35357937 DOI: 10.1126/science.abo5367  0.48
2020 Church DM. Thousands of human sequences provide deep insight into single genomes Nature. 581: 385-386. PMID 32461645 DOI: 10.1038/D41586-020-01485-4  0.555
2020 Bayega A, Djambazian H, Tsoumani KT, Gregoriou M, Sagri E, Drosopoulou E, Mavragani-Tsipidou P, Giorda K, Tsiamis G, Bourtzis K, Oikonomopoulos S, Dewar K, Church DM, Papanicolaou A, Mathiopoulos KD, et al. De novo assembly of the olive fruit fly ( Bactrocera oleae ) genome with linked-reads and long-read technologies minimizes gaps and provides exceptional Y chromosome assembly Bmc Genomics. 21: 259-259. PMID 32228451 DOI: 10.1186/S12864-020-6672-3  0.544
2020 Zou C, Karn A, Reisch B, Nguyen A, Sun Y, Bao Y, Campbell MS, Church D, Williams S, Xu X, Ledbetter CA, Patel S, Fennell A, Glaubitz JC, Clark M, et al. Haplotyping the Vitis collinear core genome with rhAmpSeq improves marker transferability in a diverse genus. Nature Communications. 11: 413. PMID 31964885 DOI: 10.1038/S41467-019-14280-1  0.497
2019 Shi W, Massaia A, Louzada S, Handsaker J, Chow W, McCarthy S, Collins J, Hallast P, Howe K, Church DM, Yang F, Xue Y, Tyler-Smith C. Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome. Genome Biology. 20: 207. PMID 31610793 DOI: 10.1186/S13059-019-1816-Y  0.382
2019 Petti AA, Williams SR, Miller CA, Fiddes IT, Srivatsan SN, Chen DY, Fronick CC, Fulton RS, Church DM, Ley TJ. A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing. Nature Communications. 10: 3660. PMID 31413257 DOI: 10.1038/S41467-019-11591-1  0.437
2019 Chaisson MJP, Sanders AD, Zhao X, Malhotra A, Porubsky D, Rausch T, Gardner EJ, Rodriguez OL, Guo L, Collins RL, Fan X, Wen J, Handsaker RE, Fairley S, Kronenberg ZN, ... ... Church DM, et al. Multi-platform discovery of haplotype-resolved structural variation in human genomes. Nature Communications. 10: 1784. PMID 30992455 DOI: 10.1038/S41467-018-08148-Z  0.596
2019 Marks P, Garcia S, Barrio AM, Belhocine K, Bernate J, Bharadwaj R, Bjornson K, Catalanotti C, Delaney J, Fehr A, Fiddes IT, Galvin B, Heaton H, Herschleb J, Hindson C, ... ... Church DM, et al. Resolving the full spectrum of human genome variation using Linked-Reads. Genome Research. PMID 30894395 DOI: 10.1101/Gr.234443.118  0.58
2019 Church DM. Genomes for all. Nature Biotechnology. 36: 815-816. PMID 30188541 DOI: 10.1038/nbt.4244  0.434
2018 Weisenfeld NI, Kumar V, Shah P, Church DM, Jaffe DB. Corrigendum: Direct determination of diploid genome sequences. Genome Research. 28: 606.1. PMID 29610250 DOI: 10.1101/Gr.235812.118  0.559
2018 Aneichyk T, Hendriks WT, Yadav R, Shin D, Gao D, Vaine CA, Collins RL, Domingo A, Currall B, Stortchevoi A, Multhaupt-Buell T, Penney EB, Cruz L, Dhakal J, Brand H, ... ... Church DM, et al. Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly. Cell. 172: 897-909.e21. PMID 29474918 DOI: 10.1016/J.Cell.2018.02.011  0.426
2018 Hulse-Kemp AM, Maheshwari S, Stoffel K, Hill TA, Jaffe D, Williams SR, Weisenfeld N, Ramakrishnan S, Kumar V, Shah P, Schatz MC, Church DM, Van Deynze A. Reference quality assembly of the 3.5-Gb genome of Capsicum annuum from a single linked-read library. Horticulture Research. 5: 4. PMID 29423234 DOI: 10.1038/S41438-017-0011-0  0.476
2018 Petti AA, Williams SR, Miller CA, Fiddes IT, Chen D, Nonavinkere Srivatsan S, Fronick C, Fulton R, Church DM, Ley TJ. Direct Detection of Expressed Mutations in AML Cells Using Single Cell RNA-Sequencing, and Its Impact on Defining Sources of Expression Heterogeneity Blood. 132: 1314-1314. DOI: 10.1182/Blood-2018-99-119075  0.391
2018 Catalanotti C, Garcia S, Belhocine K, Kumar V, Dzakula Z, Price A, Maheshwar S, Yin Y, Schnall-Levin M, Bharadwaj R, Le SA, Church DM. Abstract 3400: Characterizing genomic variation and tumor heterogeneity in cancer Cancer Research. 78: 3400-3400. DOI: 10.1158/1538-7445.Am2018-3400  0.539
2017 Schneider VA, Graves-Lindsay T, Howe K, Bouk N, Chen HC, Kitts PA, Murphy TD, Pruitt KD, Thibaud-Nissen F, Albracht D, Fulton RS, Kremitzki M, Magrini V, Markovic C, McGrath S, ... ... Church DM, et al. Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly. Genome Research. PMID 28396521 DOI: 10.1101/Gr.213611.116  0.56
2017 Weisenfeld NI, Kumar V, Shah P, Church DM, Jaffe DB. Direct determination of diploid genome sequences. Genome Research. PMID 28381613 DOI: 10.1101/Gr.214874.116  0.528
2017 Lubin IM, Aziz N, Babb LJ, Ballinger D, Bisht H, Church DM, Cordes S, Eilbeck K, Hyland F, Kalman L, Landrum M, Lockhart ER, Maglott D, Marth G, Pfeifer JD, et al. Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings. The Journal of Molecular Diagnostics : Jmd. PMID 28315672 DOI: 10.1016/J.Jmoldx.2016.12.001  0.527
2017 Yen JL, Garcia S, Montana A, Harris J, Chervitz S, Morra M, West J, Chen R, Church DM. A variant by any name: quantifying annotation discordance across tools and clinical databases. Genome Medicine. 9: 7. PMID 28122645 DOI: 10.1186/S13073-016-0396-7  0.514
2016 Jäger M, Schubach M, Zemojtel T, Reinert K, Church DM, Robinson PN. Alternate-locus aware variant calling in whole genome sequencing. Genome Medicine. 8: 130. PMID 27964746 DOI: 10.1186/S13073-016-0383-Z  0.574
2016 Helman E, Clark MJ, Alla R, Boyle S, Virk S, Luo S, Leng N, Church D, Chen R. Effect of assaying the matched normal on clinical cancer sequencing results. Journal of Clinical Oncology. 34: 11561-11561. DOI: 10.1200/Jco.2016.34.15_Suppl.11561  0.363
2016 Boyle SM, Clark MJ, Alla R, Luo S, Church DM, Helman E, Sripakdeevong P, West J, Chen R. Abstract 533: Accurately identifying expressed somatic variants for neoantigen detection and immuno-oncology Cancer Research. 76: 533-533. DOI: 10.1158/1538-7445.Am2016-533  0.388
2016 Alla R, Luo S, Helman E, Boyle SM, Clark MJ, Scott K, Sripakdeevong P, Karbelashvili M, Church DM, Snyder M, West J, Chen R. Abstract 3616: Fix the fixation: effect of formalin fixation on targeted sequencing, variant calling and gene expression Cancer Research. 76: 3616-3616. DOI: 10.1158/1538-7445.Am2016-3616  0.394
2016 Yen J, Garcia S, Clark M, Chervitz S, Linebaugh B, Montana A, West J, Chen R, Church D. Abstract 3612: Challenges in variant searching and annotation for clinical cancer testing Cancer Research. 76: 3612-3612. DOI: 10.1158/1538-7445.Am2016-3612  0.483
2016 Helman E, Clark MJ, Alla R, Boyle SM, Luo S, Virk S, Church D, Sripakdeevong P, Harris J, karbelashvili M, Haudenschild C, West J, Chen R. Abstract 3169: The benefits and burdens of assaying matched normal tissue when sequencing cancer genomes Cancer Research. 76: 3169-3169. DOI: 10.1158/1538-7445.Am2016-3169  0.427
2016 Jabara CB, Ordonez H, Giorda K, Yousif I, Church DM, Schnall-Levin M. Enabling More Complete Genome Analysis Using 10x Linked-Reads Cancer Genetics. 209: 297. DOI: 10.1016/J.Cancergen.2016.04.045  0.476
2015 Kitts PA, Church DM, Thibaud-Nissen F, Choi J, Hem V, Sapojnikov V, Smith RG, Tatusova T, Xiang C, Zherikov A, DiCuccio M, Murphy TD, Pruitt KD, Kimchi A. Assembly: a resource for assembled genomes at NCBI. Nucleic Acids Research. PMID 26578580 DOI: 10.1093/Nar/Gkv1226  0.512
2015 Patwardhan A, Harris J, Leng N, Bartha G, Church DM, Luo S, Haudenschild C, Pratt M, Zook J, Salit M, Tirch J, Morra M, Chervitz S, Li M, Clark M, et al. Achieving high-sensitivity for clinical applications using augmented exome sequencing. Genome Medicine. 7: 71. PMID 26269718 DOI: 10.1186/S13073-015-0197-4  0.558
2015 Church DM, Schneider VA, Steinberg KM, Schatz MC, Quinlan AR, Chin CS, Kitts PA, Aken B, Marth GT, Hoffman MM, Herrero J, Mendoza ML, Durbin R, Flicek P. Extending reference assembly models. Genome Biology. 16: 13. PMID 25651527 DOI: 10.1186/S13059-015-0587-3  0.554
2015 Clark MJ, Helman E, Boyle S, Luo S, Church D, Harris J, Karbelashvili M, Chervitz S, Sripakdeevong P, Bartha G, Patwardhan AJ, West J, Chen R. The detection of clinically relevant cancer mutations using a high depth, augmented, comprehensive cancer gene panel. Journal of Clinical Oncology. 33: e12547-e12547. DOI: 10.1200/Jco.2015.33.15_Suppl.E12547  0.42
2015 Helman E, Clark MJ, Boyle S, Chen R, Luo S, Haudenschild C, Harris J, Bartha G, Church D, West J. Abstract A2-39: Augmented targeted NGS in cancer diagnostics: Comparing gene panels and whole exome sequencing for accurate detection of driver mutations Cancer Research. 75. DOI: 10.1158/1538-7445.Transcagen-A2-39  0.465
2015 Clark MJ, Boyle SM, Helman E, Luo S, Bartha G, Morra M, Patwardhan A, Haudenschild C, Karbelashvili M, Sripakdeevong P, Harris J, Church D, Chervitz S, West J, Chen R. Abstract 4744: Solving genomic assay trade-offs with an optimized, extended cancer gene panel for research and clinical applications Cancer Research. 75: 4744-4744. DOI: 10.1158/1538-7445.Am2015-4744  0.497
2015 Helman E, Wick MJ, Clark MJ, Gamez L, Boyle S, Papadopoulos KP, Luo S, Tolcher AW, Sripakdeevong P, Karbelashvili M, Church D, Chen R, West J. Abstract 1457: Genomic characterization of a PDX model of T-DM1-resistant HER2+ invasive ductal carcinoma using augmented exome sequencing Cancer Research. 75: 1457-1457. DOI: 10.1158/1538-7445.Am2015-1457  0.381
2014 Steinberg KM, Schneider VA, Graves-Lindsay TA, Fulton RS, Agarwala R, Huddleston J, Shiryev SA, Morgulis A, Surti U, Warren WC, Church DM, Eichler EE, Wilson RK. Single haplotype assembly of the human genome from a hydatidiform mole. Genome Research. 24: 2066-76. PMID 25373144 DOI: 10.1101/Gr.180893.114  0.578
2014 Landrum MJ, Lee JM, Riley GR, Jang W, Rubinstein WS, Church DM, Maglott DR. ClinVar: public archive of relationships among sequence variation and human phenotype. Nucleic Acids Research. 42: D980-5. PMID 24234437 DOI: 10.1093/Nar/Gkt1113  0.444
2014 Patwardhan AJ, Helman E, Clark M, Church D, Boyle S, Pratt M, Luo S, Leng N, Haudenschild C, Chen R, West J. Accuracy and content-enhanced exome and transcriptome sequencing to guide therapeutic decision making in cancer treatment. Journal of Clinical Oncology. 32. DOI: 10.1200/Jco.2014.32.15_Suppl.E22107  0.374
2014 Clark MJ, Church D, Pratt M, Helman E, Bartha G, Chervitz S, Garcia S, Luo S, Harris J, Patwardhan A, Chen R, West J. Abstract 3576: Creating and accurately interpreting clinical grade cancer exomes: Challenges and solutions Cancer Research. 74: 3576-3576. DOI: 10.1158/1538-7445.Am2014-3576  0.528
2013 Schneider VA, Chen HC, Clausen C, Meric PA, Zhou Z, Bouk N, Husain N, Maglott DR, Church DM. Clone DB: an integrated NCBI resource for clone-associated data. Nucleic Acids Research. 41: D1070-8. PMID 23193260 DOI: 10.1093/Nar/Gks1164  0.512
2012 Sneddon TP, Church DM. Online resources for genomic structural variation. Methods in Molecular Biology (Clifton, N.J.). 838: 273-89. PMID 22228017 DOI: 10.1007/978-1-61779-507-7_13  0.546
2012 Sayers EW, Barrett T, Benson DA, Bolton E, Bryant SH, Canese K, Chetvernin V, Church DM, Dicuccio M, Federhen S, Feolo M, Fingerman IM, Geer LY, Helmberg W, Kapustin Y, et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Research. 40: D13-25. PMID 22140104 DOI: 10.1093/nar/gkr1184  0.342
2012 Riggs ER, Church DM, Hanson K, Horner VL, Kaminsky EB, Kuhn RM, Wain KE, Williams ES, Aradhya S, Kearney HM, Ledbetter DH, South ST, Thorland EC, Martin CL. Towards an evidence-based process for the clinical interpretation of copy number variation. Clinical Genetics. 81: 403-12. PMID 22097934 DOI: 10.1111/J.1399-0004.2011.01818.X  0.426
2011 Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, et al. An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 777-84. PMID 21844811 DOI: 10.1097/Gim.0B013E31822C79F9  0.424
2011 Church DM, Schneider VA, Graves T, Auger K, Cunningham F, Bouk N, Chen HC, Agarwala R, McLaren WM, Ritchie GR, Albracht D, Kremitzki M, Rock S, Kotkiewicz H, Kremitzki C, et al. Modernizing reference genome assemblies. Plos Biology. 9: e1001091. PMID 21750661 DOI: 10.1371/Journal.Pbio.1001091  0.375
2011 Sayers EW, Barrett T, Benson DA, Bolton E, Bryant SH, Canese K, Chetvernin V, Church DM, DiCuccio M, Federhen S, Feolo M, Fingerman IM, Geer LY, Helmberg W, Kapustin Y, et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Research. 39: D38-51. PMID 21097890 DOI: 10.1093/nar/gkq1172  0.356
2010 Church DM, Lappalainen I, Sneddon TP, Hinton J, Maguire M, Lopez J, Garner J, Paschall J, DiCuccio M, Yaschenko E, Scherer SW, Feuk L, Flicek P. Public data archives for genomic structural variation. Nature Genetics. 42: 813-4. PMID 20877315 DOI: 10.1038/Ng1010-813  0.469
2010 Sayers EW, Barrett T, Benson DA, Bolton E, Bryant SH, Canese K, Chetvernin V, Church DM, Dicuccio M, Federhen S, Feolo M, Geer LY, Helmberg W, Kapustin Y, Landsman D, et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Research. 38: D5-16. PMID 19910364 DOI: 10.1093/nar/gkp967  0.375
2010 Wang X, Agarwala R, Capra JA, Chen Z, Church DM, Ciobanu DC, Li Z, Lu L, Mozhui K, Mulligan MK, Nelson SF, Pollard KS, Taylor WL, Thomason DB, Williams RW. High-throughput sequencing of the DBA/2J mouse genome Bmc Bioinformatics. 11. DOI: 10.1186/1471-2105-11-S4-O7  0.503
2009 Church DM, Goodstadt L, Hillier LW, Zody MC, Goldstein S, She X, Bult CJ, Agarwala R, Cherry JL, DiCuccio M, Hlavina W, Kapustin Y, Meric P, Maglott D, Birtle Z, et al. Lineage-specific biology revealed by a finished genome assembly of the mouse. Plos Biology. 7: e1000112. PMID 19468303 DOI: 10.1371/Journal.Pbio.1000112  0.584
2009 Church DM, Hillier LW. Back to Bermuda: how is science best served? Genome Biology. 10: 105. PMID 19435531 DOI: 10.1186/Gb-2009-10-4-105  0.37
2009 Sayers EW, Barrett T, Benson DA, Bryant SH, Canese K, Chetvernin V, Church DM, DiCuccio M, Edgar R, Federhen S, Feolo M, Geer LY, Helmberg W, Kapustin Y, Landsman D, et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Research. 37: D5-15. PMID 18940862 DOI: 10.1093/nar/gkn741  0.328
2008 She X, Cheng Z, Zöllner S, Church DM, Eichler EE. Mouse segmental duplication and copy number variation. Nature Genetics. 40: 909-14. PMID 18500340 DOI: 10.1038/Ng.172  0.498
2008 Wheeler DL, Barrett T, Benson DA, Bryant SH, Canese K, Chetvernin V, Church DM, Dicuccio M, Edgar R, Federhen S, Feolo M, Geer LY, Helmberg W, Kapustin Y, Khovayko O, et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Research. 36: D13-21. PMID 18045790 DOI: 10.1093/nar/gkm1000  0.375
2007 Birney E, Stamatoyannopoulos JA, Dutta A, Guigó R, Gingeras TR, Margulies EH, Weng Z, Snyder M, Dermitzakis ET, Thurman RE, Kuehn MS, Taylor CM, Neph S, Koch CM, ... ... Church D, et al. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature. 447: 799-816. PMID 17571346 DOI: 10.1038/Nature05874  0.524
2007 Eichler EE, Nickerson DA, Altshuler D, Bowcock AM, Brooks LD, Carter NP, Church DM, Felsenfeld A, Guyer M, Lee C, Lupski JR, Mullikin JC, Pritchard JK, Sebat J, et al. Completing the map of human genetic variation. Nature. 447: 161-5. PMID 17495918 DOI: 10.1038/447161A  0.524
2007 Wheeler DL, Barrett T, Benson DA, Bryant SH, Canese K, Chetvernin V, Church DM, DiCuccio M, Edgar R, Federhen S, Geer LY, Kapustin Y, Khovayko O, Landsman D, Lipman DJ, et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Research. 35: D5-12. PMID 17170002 DOI: 10.1093/nar/gkl1031  0.368
2006 Frankenberger C, Wu X, Harmon J, Church D, Gangi LM, Munroe DJ, Urzúa U. WebaCGH: an interactive online tool for the analysis and display of array comparative genomic hybridisation data. Applied Bioinformatics. 5: 125-30. PMID 16722779 DOI: 10.2165/00822942-200605020-00009  0.353
2006 Wheeler DL, Barrett T, Benson DA, Bryant SH, Canese K, Chetvernin V, Church DM, DiCuccio M, Edgar R, Federhen S, Geer LY, Helmberg W, Kapustin Y, Kenton DL, Khovayko O, et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Research. 34: D173-80. PMID 16381840 DOI: 10.1093/nar/gkj158  0.33
2005 Cheng Z, Ventura M, She X, Khaitovich P, Graves T, Osoegawa K, Church D, DeJong P, Wilson RK, Pääbo S, Rocchi M, Eichler EE. A genome-wide comparison of recent chimpanzee and human segmental duplications. Nature. 437: 88-93. PMID 16136132 DOI: 10.1038/Nature04000  0.49
2005 Wheeler DL, Barrett T, Benson DA, Bryant SH, Canese K, Church DM, DiCuccio M, Edgar R, Federhen S, Helmberg W, Kenton DL, Khovayko O, Lipman DJ, Madden TL, Maglott DR, et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Research. 33: D39-45. PMID 15608222 DOI: 10.1093/nar/gki062  0.331
2004 She X, Jiang Z, Clark RA, Liu G, Cheng Z, Tuzun E, Church DM, Sutton G, Halpern AL, Eichler EE. Shotgun sequence assembly and recent segmental duplications within the human genome. Nature. 431: 927-30. PMID 15496912 DOI: 10.1038/Nature03062  0.586
2004 Salzberg SL, Church D, DiCuccio M, Yaschenko E, Ostell J. The genome Assembly Archive: a new public resource. Plos Biology. 2: E285. PMID 15367931 DOI: 10.1371/Journal.Pbio.0020285  0.588
2004 Bailey JA, Church DM, Ventura M, Rocchi M, Eichler EE. Analysis of segmental duplications and genome assembly in the mouse. Genome Research. 14: 789-801. PMID 15123579 DOI: 10.1101/Gr.2238404  0.555
2004 Wheeler DL, Church DM, Edgar R, Federhen S, Helmberg W, Madden TL, Pontius JU, Schuler GD, Schriml LM, Sequeira E, Suzek TO, Tatusova TA, Wagner L. Database resources of the National Center for Biotechnology Information: update. Nucleic Acids Research. 32: D35-40. PMID 14681353 DOI: 10.1093/Nar/Gkh073  0.428
2003 Baldarelli RM, Hill DP, Blake JA, Adachi J, Furuno M, Bradt D, Corbani LE, Cousins S, Frazer KS, Qi D, Yang L, Ramachandran S, Reed D, Zhu Y, Kasukawa T, ... ... Church DM, et al. Connecting sequence and biology in the laboratory mouse. Genome Research. 13: 1505-19. PMID 12819150 DOI: 10.1101/Gr.991003  0.582
2003 Frazer KA, Elnitski L, Church DM, Dubchak I, Hardison RC. Cross-species sequence comparisons: a review of methods and available resources. Genome Research. 13: 1-12. PMID 12529301 DOI: 10.1101/Gr.222003  0.465
2003 Wheeler DL, Church DM, Federhen S, Lash AE, Madden TL, Pontius JU, Schuler GD, Schriml LM, Sequeira E, Tatusova TA, Wagner L. Database resources of the National Center for Biotechnology. Nucleic Acids Research. 31: 28-33. PMID 12519941 DOI: 10.1093/Nar/Gkg033  0.464
2003 Marth G, Schuler G, Yeh R, Davenport R, Agarwala R, Church D, Wheelan S, Baker J, Ward M, Kholodov M, Phan L, Czabarka E, Murvai J, Cutler D, Wooding S, et al. Sequence variations in the public human genome data reflect a bottlenecked population history. Proceedings of the National Academy of Sciences of the United States of America. 100: 376-81. PMID 12502794 DOI: 10.1073/Pnas.222673099  0.56
2002 Church D, Pruitt KD. Accessing the human genome. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 6.9. PMID 18428332 DOI: 10.1002/0471142905.Hg0609S34  0.569
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, ... ... Church DM, et al. Initial sequencing and comparative analysis of the mouse genome. Nature. 420: 520-62. PMID 12466850 DOI: 10.1038/Nature01262  0.598
2002 Wheeler DL, Church DM, Lash AE, Leipe DD, Madden TL, Pontius JU, Schuler GD, Schriml LM, Tatusova TA, Wagner L, Rapp BA. Database resources of the National Center for Biotechnology Information: 2002 update. Nucleic Acids Research. 30: 13-6. PMID 11752242  0.404
2001 Wheelan SJ, Church DM, Ostell JM. Spidey: a tool for mRNA-to-genomic alignments. Genome Research. 11: 1952-7. PMID 11691860 DOI: 10.1101/Gr.195301  0.579
2001 Hudson TJ, Church DM, Greenaway S, Nguyen H, Cook A, Steen RG, Van Etten WJ, Castle AB, Strivens MA, Trickett P, Heuston C, Davison C, Southwell A, Hardisty R, Varela-Carver A, et al. A radiation hybrid map of mouse genes. Nature Genetics. 29: 201-5. PMID 11586302 DOI: 10.1038/Ng1001-201  0.507
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, ... ... Church D, et al. Initial sequencing and analysis of the human genome. Nature. 409: 860-921. PMID 11237011 DOI: 10.1038/35057062  0.57
2001 Wheeler DL, Church DM, Lash AE, Leipe DD, Madden TL, Pontius JU, Schuler GD, Schriml LM, Tatusova TA, Wagner L, Rapp BA. Database resources of the National Center for Biotechnology Information. Nucleic Acids Research. 29: 11-6. PMID 11125038  0.431
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, ... ... Church D, et al. Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921)) Nature. 412: 565-566. DOI: 10.1038/35087627  0.569
2000 LePage DF, Church DM, Millie E, Hassold TJ, Conlon RA. Rapid generation of nested chromosomal deletions on mouse chromosome 2. Proceedings of the National Academy of Sciences of the United States of America. 97: 10471-6. PMID 10984539 DOI: 10.1073/Pnas.97.19.10471  0.335
1994 Church DM, Stotler CJ, Rutter JL, Murrell JR, Trofatter JA, Buckler AJ. Isolation of genes from complex sources of mammalian genomic DNA using exon amplification. Nature Genetics. 6: 98-105. PMID 8136842 DOI: 10.1038/ng0194-98  0.311
1993 Church DM, Banks LT, Rogers AC, Graw SL, Housman DE, Gusella JF, Buckler AJ. Identification of human chromosome 9 specific genes using exon amplification. Human Molecular Genetics. 2: 1915-20. PMID 7506603 DOI: 10.1093/hmg/2.11.1915  0.477
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