Lucinda Antonacci-Fulton

Research output

Research output per year 1993 2018 2022

• 177 Article
• 18 Comment/debate
• 5 Review article
• 1 Letter

Research output per year

Research output per year

Search results

• 2022

  Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

  TOPMed Anthropometry Working Group & NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Mar 2022, In: Nature Genetics. 54, 3, p. 263-273 11 p.

  Research output: Contribution to journal › Article › peer-review

  • Multifactorial Inheritance 100%
  • Linkage Disequilibrium 92%
  • Single Nucleotide Polymorphism 67%
  • Body Mass Index 58%
  • Genome 54%
  32 Scopus citations

• Author Correction: Comparative and demographic analysis of orang-utan genomes (Nature, (2011), 469, 7331, (529-533), 10.1038/nature09687)

  Locke, D. P., Hillier, L. D. W., Warren, W. C., Worley, K. C., Nazareth, L. V., Muzny, D. M., Yang, S. P., Wang, Z., Chinwalla, A. T., Minx, P., Mitreva, M., Cook, L., Delehaunty, K. D., Fronick, C., Schmidt, H., Fulton, L. A., Fulton, R. S., Nelson, J. O., Magrini, V., Pohl, C., & 81 othersGraves, T. A., Markovic, C., Cree, A., Dinh, H. H., Hume, J., Kovar, C. L., Fowler, G. R., Lunter, G., Meader, S., Heger, A., Ponting, C. P., Marques-Bonet, T., Alkan, C., Chen, L., Cheng, Z., Kidd, J. M., Eichler, E. E., White, S., Searle, S., Vilella, A. J., Chen, Y., Flicek, P., Ma, J., Raney, B., Suh, B., Burhans, R., Herrero, J., Haussler, D., Faria, R., Fernando, O., Darré, F., Farré, D., Gazave, E., Oliva, M., Navarro, A., Roberto, R., Capozzi, O., Archidiacono, N., Della Valle, G., Purgato, S., Rocchi, M., Konkel, M. K., Walker, J. A., Ullmer, B., Batzer, M. A., Smit, A. F. A., Hubley, R., Casola, C., Schrider, D. R., Hahn, M. W., Quesada, V., Puente, X. S., Ordoñez, G. R., López-Otín, C., Vinar, T., Brejova, B., Ratan, A., Harris, R. S., Miller, W., Kosiol, C., Lawson, H. A., Taliwal, V., Martins, A. L., Siepel, A., RoyChoudhury, A., Ma, X., Degenhardt, J., Bustamante, C. D., Gutenkunst, R. N., Mailund, T., Dutheil, J. Y., Hobolth, A., Schierup, M. H., Ryder, O. A., Yoshinaga, Y., de Jong, P. J., Weinstock, G. M., Rogers, J., Mardis, E. R., Gibbs, R. A. & Wilson, R. K., Aug 25 2022, In: Nature. 608, 7924, p. E36

  Research output: Contribution to journal › Comment/debate

  Open Access

  • Genome 100%
  • Demography 95%
  • Single Nucleotide Polymorphism 82%
  • Publications 81%
  • Names 46%

• Nine out of ten samples were mistakenly switched by The Orang-utan Genome Consortium

  Banes, G. L., Fountain, E. D., Karklus, A., Fulton, R., Antonacci-Fulton, L. & Nelson, J. O., Dec 2022, In: Scientific data. 9, 1, 485.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Genome 100%
  • Consortium 97%
  • Genomics 94%
  • Comparative Genomics 28%
  • Sequencing 25%

• Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

  AMP-T2D-GENES, Myocardial Infarction Genetics Consortium, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium & NHLBI TOPMed Lipids Working Group, Jan 6 2022, In: American journal of human genetics. 109, 1, p. 81-96 16 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Exome 100%
  • Lipids 54%
  • Genes 33%
  • Genome-Wide Association Study 20%
  • Hispanic Americans 12%
  7 Scopus citations

• Spatially restricted drivers and transitional cell populations cooperate with the microenvironment in untreated and chemo-resistant pancreatic cancer

  Cui Zhou, D., Jayasinghe, R. G., Chen, S., Herndon, J. M., Iglesia, M. D., Navale, P., Wendl, M. C., Caravan, W., Sato, K., Storrs, E., Mo, C. K., Liu, J., Southard-Smith, A. N., Wu, Y., Naser Al Deen, N., Baer, J. M., Fulton, R. S., Wyczalkowski, M. A., Liu, R., Fronick, C. C., & 46 othersFulton, L. A., Shinkle, A., Thammavong, L., Zhu, H., Sun, H., Wang, L. B., Li, Y., Zuo, C., McMichael, J. F., Davies, S. R., Appelbaum, E. L., Robbins, K. J., Chasnoff, S. E., Yang, X., Reeb, A. N., Oh, C., Serasanambati, M., Lal, P., Varghese, R., Mashl, J. R., Ponce, J., Terekhanova, N. V., Yao, L., Wang, F., Chen, L., Schnaubelt, M., Lu, R. J. H., Schwarz, J. K., Puram, S. V., Kim, A. H., Song, S. K., Shoghi, K. I., Lau, K. S., Ju, T., Chen, K., Chatterjee, D., Hawkins, W. G., Zhang, H., Achilefu, S., Chheda, M. G., Oh, S. T., Gillanders, W. E., Chen, F., DeNardo, D. G., Fields, R. C. & Ding, L., Sep 2022, In: Nature Genetics. 54, 9, p. 1390-1405 16 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Pancreatic Neoplasms 100%
  • Population 41%
  • Neoplasms 34%
  • Proteogenomics 29%
  • Adenocarcinoma 27%
  5 Scopus citations

• The Human Pangenome Project: a global resource to map genomic diversity

  Human Pangenome Reference Consortium, Apr 1 2022, In: Nature. 604, 7906, p. 437-446 10 p.

  Research output: Contribution to journal › Review article › peer-review

  Open Access

  • Telomere 100%
  • Human Genome 95%
  • Genome 61%
  • Human Genetics 55%
  • Nucleic Acid Repetitive Sequences 55%
  20 Scopus citations

• Whole genome sequence analysis of blood lipid levels in >66,000 individuals

  NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 2022, In: Nature communications. 13, 1, 5995.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • genome 100%
  • lipids 75%
  • blood 73%
  • Sequence Analysis 71%
  • Lipid 52%
• 2021

  A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

  NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Oct 2021, In: Nature Genetics. 53, 10, p. 1504-1516 13 p.

  Research output: Contribution to journal › Article › peer-review

  • HIV 100%
  • HLA-B Antigens 61%
  • Population 56%
  • Hispanic Americans 46%
  • Genome-Wide Association Study 25%
  9 Scopus citations

• Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (Nature, (2020), 586, 7831, (763-768), 10.1038/s41586-020-2819-2)

  NHLBI Trans-Omics for Precision Medicine Consortium, Mar 25 2021, In: Nature. 591, 7851, p. E27

  Research output: Contribution to journal › Comment/debate

  Open Access

  • Hematopoiesis 100%
  • Genome 62%
  • Medical Oncology 54%
  • Computational Biology 43%
  • Neoplasms 14%
  2 Scopus citations

• Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response (Nature Genetics, (2021), 53, 10, (1504-1516), 10.1038/s41588-021-00935-7)

  NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 2021, In: Nature Genetics. 53, 12, p. 1722 1 p.

  Research output: Contribution to journal › Comment/debate

  Open Access

  • Seoul 100%
  • HIV 53%
  • Republic of Korea 46%
  • Population 30%
  • Bioengineering 25%

• Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

  NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium & FinnGen, Dec 1 2021, In: Nature communications. 12, 1, 2182.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • chromosomes 100%
  • lipids 80%
  • Chromosomes 64%
  • blood 62%
  • Lipid 56%
  6 Scopus citations

• Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium

  NHLBI SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS), Dec 2021, In: Genome medicine. 13, 1, 66.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • SARS Virus 100%
  • Epithelium 51%
  • Viruses 33%
  • Gene Expression 30%
  • Genes 27%
  10 Scopus citations

• Genome sequencing unveils a regulatory landscape of platelet reactivity

  NHLBI Trans-Omics for Precision (TOPMed) Consortium, Dec 1 2021, In: Nature communications. 12, 1, 3626.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • sequencing 100%
  • genome 95%
  • loci 82%
  • platelets 79%
  • reactivity 73%
  11 Scopus citations

• Genomic Profiling of Lung Adenocarcinoma in Never-Smokers

  Devarakonda, S., Li, Y., Martins Rodrigues, F., Sankararaman, S., Kadara, H., Goparaju, C., Lanc, I., Pepin, K., Waqar, S. N., Morgensztern, D., Ward, J., Masood, A., Fulton, R., Fulton, L., Gillette, M. A., Satpathy, S., Carr, S. A., Wistuba, I., Pass, H., Wilson, R. K., & 2 othersDing, L. & Govindan, R., Nov 20 2021, In: Journal of Clinical Oncology. 39, 33, p. 3747-3758 12 p.

  Research output: Contribution to journal › Article › peer-review

  • Adenocarcinoma of Lung 100%
  • Smokers 79%
  • RNA Sequence Analysis 19%
  • Whole Exome Sequencing 13%
  • Smoke 11%
  10 Scopus citations

• Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

  NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Feb 11 2021, In: Nature. 590, 7845, p. 290-299 10 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • National Heart, Lung, and Blood Institute (U.S.) 100%
  • Precision Medicine 79%
  • Genome 49%
  • Genotype 21%
  • Catalogs 18%
  361 Scopus citations

• Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

  NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 1 2021, In: Nature communications. 12, 1, 3506.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Whole Genome Sequencing 100%
  • stratification 98%
  • Economic Inflation 96%
  • Hemoglobin 79%
  • sequencing 58%

• Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

  TOPMed Sleep Working Group & NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 2021, In: Genome medicine. 13, 1, 136.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • National Heart, Lung, and Blood Institute (U.S.) 100%
  • Sleep Apnea Syndromes 79%
  • Precision Medicine 79%
  • Genome-Wide Association Study 76%
  • Oxyhemoglobins 48%
  2 Scopus citations
• 2020

  Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (Nature Communications, (2020), 11, 1, (4748), 10.1038/s41467-020-18151-y)

  MC3 Working Group, PCAWG novel somatic mutation calling methods working group & PCAWG Consortium, Dec 1 2020, In: Nature communications. 11, 1, 6232.

  Research output: Contribution to journal › Comment/debate

  Open Access

  • genome 100%
  • Exome 92%
  • mutations 89%
  • medicine 82%
  • cancer 71%

• Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (Molecular Psychiatry, (2020), 25, 8, (1859-1875), 10.1038/s41380-018-0112-7)

  Alzheimer’s Disease Sequencing Project, Aug 1 2020, In: Molecular Psychiatry. 25, 8, p. 1901-1903 3 p.

  Research output: Contribution to journal › Comment/debate

  Open Access

  • Whole Exome Sequencing 100%
  • Publications 69%
  • Psychiatry 62%
  4 Scopus citations

• Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

  NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium & TOPMed Lipids Working Group, Sep 1 2020, In: Nature Genetics. 52, 9, p. 969-983 15 p.

  Research output: Contribution to journal › Article › peer-review

  • Whole Genome Sequencing 100%
  • Computer Simulation 81%
  • Intergenic DNA 55%
  • Precision Medicine 46%
  • LDL Cholesterol 38%
  51 Scopus citations

• Inherited causes of clonal haematopoiesis in 97,691 whole genomes

  NHLBI Trans-Omics for Precision Medicine Consortium, Oct 29 2020, In: Nature. 586, 7831, p. 763-768 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Hematopoiesis 100%
  • Genome 62%
  • Hematopoietic Stem Cells 45%
  • National Heart, Lung, and Blood Institute (U.S.) 20%
  • Genetic Loci 18%
  182 Scopus citations

• Mapping and characterization of structural variation in 17,795 human genomes

  NHGRI Centers for Common Disease Genomics, Jul 2 2020, In: Nature. 583, 7814, p. 83-89 7 p.

  Research output: Contribution to journal › Article › peer-review

  • Whole Genome Sequencing 100%
  • Human Genome 90%
  • Alleles 62%
  • Genome 38%
  • Human Genetics 35%
  78 Scopus citations

• Pan-cancer analysis of whole genomes

  The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium, Feb 6 2020, In: Nature. 578, 7793, p. 82-93 12 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Genome 100%
  • Neoplasms 47%
  • Mutation 21%
  • Telomere 21%
  • Point Mutation 19%
  1038 Scopus citations

• Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (Nature Communications, (2018), 9, 1, (2606), 10.1038/s41467-018-04668-w)

  NHLBI TOPMed Lipids Working Group, Dec 1 2020, In: Nature communications. 11, 1, 1715.

  Research output: Contribution to journal › Comment/debate

  Open Access

  • lipoproteins 100%
  • genome 89%
  • Lipoprotein(a) 84%
  • Lipoprotein 75%
  • Communication 62%
  1 Scopus citations

• Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

  MC3 Working Group, PCAWG novel somatic mutation calling methods working group & PCAWG Consortium, Dec 1 2020, In: Nature communications. 11, 1, 4748.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • genome 100%
  • Exome 92%
  • mutations 89%
  • sequencing 87%
  • cancer 71%
  18 Scopus citations

• Sequence analysis in Bos taurus reveals pervasiveness of X–Y arms races in mammalian lineages

  Hughes, J. F., Skaletsky, H., Pyntikova, T., Koutseva, N., Raudsepp, T., Brown, L. G., Bellott, D. W., Cho, T. J., Dugan-Rocha, S., Khan, Z., Kremitzki, C., Fronick, C., Graves-Lindsay, T. A., Fulton, L., Warren, W. C., Wilson, R. K., Owens, E., Womack, J. E., Murphy, W. J., Muzny, D. M., & 4 othersWorley, K. C., Chowdhary, B. P., Gibbs, R. A. & Page, D. C., Nov 18 2020, In: Genome research. 31, 12, p. 1716-1726 11 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Sequence Analysis 100%
  • Cattle 86%
  • Genetic Crossing Over 76%
  • Sex Chromosomes 70%
  • Y Chromosome 65%
  13 Scopus citations

• Sex differences in oncogenic mutational processes

  PCAWG Tumour Subtypes and Clinical Translation & PCAWG Consortium, Dec 1 2020, In: Nature communications. 11, 1, 4330.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Oncogenic 100%
  • Sex Characteristics 66%
  • Mutation 60%
  • cancer 57%
  • genome 39%
  33 Scopus citations

• Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

  Alzheimer’s Disease Sequencing Project, Aug 1 2020, In: Molecular Psychiatry. 25, 8, p. 1859-1875 17 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Whole Exome Sequencing 100%
  • Alzheimer Disease 65%
  • Hispanic Americans 20%
  • Alzheimer Disease 5 17%
  • Genes 16%
  114 Scopus citations
• 2019

  A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease

  Alzheimer's Disease Sequencing Project, Mar 2019, In: Alzheimer's and Dementia. 15, 3, p. 441-452 12 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Alzheimer disease type 2 100%
  • dementia 66%
  • Alzheimer Disease 51%
  • Datasets 39%
  • Hispanic Americans 31%
  23 Scopus citations

• Erratum: The Immune Landscape of Cancer (Immunity (2018) 48(4) (812–830.e14), (S1074761318301213), (10.1016/j.immuni.2018.03.023))

  The Cancer Genome Atlas Research Network, Aug 20 2019, In: Immunity. 51, 2, p. 411-412 2 p.

  Research output: Contribution to journal › Comment/debate

  Open Access

  • Immunity 100%
  • Names 77%
  • Genes 49%
  • Neoplasms 39%
  • Research Design 32%
  135 Scopus citations

• Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

  National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 2019, In: CHEST. 156, 6, p. 1068-1079 12 p.

  Research output: Contribution to journal › Article › peer-review

  • Whole Genome Sequencing 100%
  • Protein Domains 86%
  • Cysteine 81%
  • Asthma 66%
  • Lung 46%
  4 Scopus citations
• 2018

  A Comprehensive Pan-Cancer Molecular Study of Gynecologic and Breast Cancers

  The Cancer Genome Atlas Research Network, Apr 9 2018, In: Cancer Cell. 33, 4, p. 690-705.e9

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Atlases 100%
  • Breast Neoplasms 99%
  • Decision Trees 77%
  • Long Noncoding RNA 67%
  • Genome 63%
  296 Scopus citations

• An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics

  The Cancer Genome Atlas Research Network, Apr 5 2018, In: Cell. 173, 2, p. 400-416.e11

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Atlases 100%
  • Genome 63%
  • Survival 51%
  • Neoplasms 30%
  • Datasets 9%
  1297 Scopus citations

• A Pan-Cancer Analysis of Enhancer Expression in Nearly 9000 Patient Samples

  The Cancer Genome Atlas Research Network, Apr 5 2018, In: Cell. 173, 2, p. 386-399.e12

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Enhancer 100%
  • Neoplasms 27%
  • Genes 14%
  • RNA-Seq 14%
  • Aneuploidy 12%
  148 Scopus citations

• A Pan-Cancer Analysis Reveals High-Frequency Genetic Alterations in Mediators of Signaling by the TGF-β Superfamily

  The Cancer Genome Atlas Research Network, Oct 24 2018, In: Cell Systems. 7, 4, p. 422-437.e7

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Transforming Growth Factors 100%
  • Sequence Deletion 31%
  • Neoplasms 30%
  • Genes 21%
  • Transforming Growth Factor-beta Type II Receptors 19%
  92 Scopus citations

• Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of Cancer

  The Cancer Genome Atlas Network, Apr 5 2018, In: Cell. 173, 2, p. 291-304.e6

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • MicroRNA 100%
  • Cluster Analysis 36%
  • Protein 33%
  • Neoplasms 26%
  • Aneuploidy 21%
  1028 Scopus citations

• Comparative Molecular Analysis of Gastrointestinal Adenocarcinomas

  The Cancer Genome Atlas Research Network, Apr 9 2018, In: Cancer Cell. 33, 4, p. 721-735.e8

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Adenocarcinoma 100%
  • Genome 49%
  • Chromosomal Instability 45%
  • Neoplasms 41%
  • Rectum 36%
  268 Scopus citations

• Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients

  The Cancer Genome Atlas Research Network, Aug 13 2018, In: Cancer Cell. 34, 2, p. 211-224.e6

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Alternative Splicing 100%
  • Neoplasms 29%
  • Exons 12%
  • Peptides 9%
  • Whole Exome Sequencing 9%
  381 Scopus citations

• Comprehensive Characterization of Cancer Driver Genes and Mutations

  The MC3 Working Group & The Cancer Genome Atlas Research Network, Apr 5 2018, In: Cell. 173, 2, p. 371-385.e18

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Neoplasm Genes 100%
  • Mutation 77%
  • Neoplasms 29%
  • Oncogenic 25%
  • Catalogs 11%
  941 Scopus citations

• Comprehensive Molecular Characterization of the Hippo Signaling Pathway in Cancer

  The Cancer Genome Atlas Research Network, Oct 30 2018, In: Cell Reports. 25, 5, p. 1304-1317.e5

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • MicroRNA 100%
  • Heterogeneity 75%
  • Mutation 68%
  • Neoplasms 26%
  • Squamous Cell Neoplasms 20%
  188 Scopus citations

• Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

  NHLBI TOPMed Lipids Working Group, Dec 1 2018, In: Nature communications. 9, 1, 3391.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Low-Density Lipoprotein Cholesterol 100%
  • sequencing 85%
  • genome 82%
  • cholesterol 80%
  • Whole Genome Sequencing 73%
  93 Scopus citations

• Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

  Zekavat, S. M., Ruotsalainen, S., Handsaker, R. E., Alver, M., Bloom, J., Poterba, T., Seed, C., Ernst, J., Chaffin, M., Engreitz, J., Peloso, G. M., Manichaikul, A., Yang, C., Ryan, K. A., Fu, M., Johnson, W. C., Tsai, M., Budoff, M., Ramachandran, V. S., Cupples, L. A., & 323 othersRotter, J. I., Rich, S. S., Post, W., Mitchell, B. D., Correa, A., Metspalu, A., Wilson, J. G., Salomaa, V., Kellis, M., Daly, M. J., Neale, B. M., McCarroll, S., Surakka, I., Esko, T., Ganna, A., Ripatti, S., Kathiresan, S., Natarajan, P., Abe, N., Abecasis, G., Albert, C., Allred, N. P., Almasy, L., Alonso, A., Ament, S., Anderson, P., Anugu, P., Applebaum-Bowden, D., Arking, D., Arnett, D. K., Ashley-Koch, A., Aslibekyan, S., Assimes, T., Auer, P., Avramopoulos, D., Barnard, J., Barnes, K., Barr, R. G., Barron-Casella, E., Beaty, T., Becker, D., Becker, L., Beer, R., Begum, F., Beitelshees, A., Benjamin, E., Bezerra, M., Bielak, L., Bis, J., Blackwell, T., Blangero, J., Boerwinkle, E., Borecki, I., Bowler, R., Brody, J., Broeckel, U., Broome, J., Bunting, K., Burchard, E., Cardwell, J., Carty, C., Casaburi, R., Casella, J., Chang, C., Chasman, D., Chavan, S., Chen, B. J., Chen, W. M., Chen, Y. D. I., Cho, M., Choi, S. H., Chuang, L. M., Chung, M., Cornell, E., Crandall, C., Crapo, J., Curran, J., Curtis, J., Custer, B., Damcott, C., Darbar, D., Das, S., David, S., Davis, C., Daya, M., Andrade, M. D., Debaun, M., Deka, R., Demeo, D., Devine, S., Do, R., Duan, Q., Duggirala, R., Durda, P., Dutcher, S., Eaton, C., Ekunwe, L., Ellinor, P., Emery, L., Farber, C., Farnam, L., Fingerlin, T., Flickinger, M., Fornage, M., Franceschini, N., Fullerton, S. M., Fulton, L., Gabriel, S., Gan, W., Gao, Y., Gass, M., Gelb, B., Geng, X., Germer, S., Gignoux, C., Gladwin, M., Glahn, D., Gogarten, S., Gong, D. W., Goring, H., Gu, C. C., Guan, Y., Guo, X., Haessler, J., Hall, M., Harris, D., Hawley, N., He, J., Heavner, B., Heckbert, S., Hernandez, R., Herrington, D., Hersh, C., Hidalgo, B., Hixson, J., Hokanson, J., Hong, E., Hoth, K., Hsiung, C., Huston, H., Hwu, C. M., Irvin, M. R., Jackson, R., Jain, D., Jaquish, C., Jhun, M. A., Johnsen, J., Johnson, A., Johnston, R., Jones, K., Kang, H. M., Kaplan, R., Kardia, S., Kaufman, L., Kelly, S., Kenny, E., Kessler, M., Khan, A., Kinney, G., Konkle, B., Kooperberg, C., Kramer, H., Krauter, S., Lange, C., Lange, E., Lange, L., Laurie, C., Laurie, C., Leboff, M., Lee, S. S., Lee, W. J., Lefaive, J., Levine, D., Levy, D., Lewis, J., Li, Y., Lin, H., Lin, K. H., Liu, S., Liu, Y., Loos, R., Lubitz, S., Lunetta, K., Luo, J., Mahaney, M., Make, B., Manson, J. A., Margolin, L., Martin, L., Mathai, S., Mathias, R., McArdle, P., McDonald, M. L., McFarland, S., McGarvey, S., Mei, H., Meyers, D. A., Mikulla, J., Min, N., Minear, M., Minster, R. L., Montasser, M. E., Musani, S., Mwasongwe, S., Mychaleckyj, J. C., Nadkarni, G., Naik, R., Nekhai, S., Nickerson, D., North, K., O'connell, J., O'connor, T., Ochs-Balcom, H., Pankow, J., Papanicolaou, G., Parker, M., Parsa, A., Penchev, S., Peralta, J. M., Perez, M., Perry, J., Peters, U., Peyser, P., Phillips, L., Phillips, S., Pollin, T., Becker, J. P., Boorgula, M. P., Preuss, M., Prokopenko, D., Psaty, B., Qasba, P., Qiao, D., Qin, Z., Rafaels, N., Raffield, L., Rao, D. C., Rasmussen-Torvik, L., Ratan, A., Redline, S., Reed, R., Regan, E., Reiner, A., Rice, K., Roden, D., Roselli, C., Ruczinski, I., Russell, P., Ruuska, S., Sakornsakolpat, P., Salimi, S., Salzberg, S., Sandow, K., Sankaran, V., Scheller, C., Schmidt, E., Schwander, K., Schwartz, D., Sciurba, F., Seidman, C., Sheehan, V., Shetty, A., Shetty, A., Sheu, W. H. H., Shoemaker, M. B., Silver, B., Silverman, E., Smith, J., Smith, J., Smith, N., Smith, T., Smoller, S., Snively, B., Sofer, T., Sotoodehnia, N., Stilp, A., Streeten, E., Sung, Y. J., Sylvia, J., Szpiro, A., Sztalryd, C., Taliun, D., Tang, H., Taub, M., Taylor, K., Taylor, S., Telen, M., Thornton, T. A., Tinker, L., Tirschwell, D., Tiwari, H., Tracy, R., Vaidya, D., Vandehaar, P., Vrieze, S., Walker, T., Wallace, R., Walts, A., Wan, E., Wang, F. F., Watson, K., Weeks, D. E., Weir, B., Weiss, S., Weng, L. C., Willer, C., Williams, K., Williams, L. K., Wilson, C., Wong, Q., Xu, H., Yanek, L., Yang, I., Yang, R., Zaghloul, N., Zhang, Y., Zhao, S. X., Zhao, W., Zheng, X., Zhi, D., Zhou, X., Zody, M. & Zoellner, S., Dec 1 2018, In: Nature communications. 9, 1, 2606.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • lipoproteins 100%
  • genome 89%
  • Lipoprotein(a) 84%
  • Lipoprotein 75%
  • Cholesterol 61%
  54 Scopus citations

• Driver Fusions and Their Implications in the Development and Treatment of Human Cancers

  The Fusion Analysis Working Group & The Cancer Genome Atlas Research Network, Apr 3 2018, In: Cell Reports. 23, 1, p. 227-238.e3

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Human Development 100%
  • Mutation 78%
  • Peptide 53%
  • Drug 48%
  • Gene Fusion 45%
  272 Scopus citations

• Erratum: Comprehensive Characterization of Cancer Driver Genes and Mutations (ARTICLE (2018) 173(2) (371–385), (S009286741830237X), (10.1016/j.cell.2018.02.060))

  The MC3 Working Group, The Cancer Genome Atlas Research Network, The MC3 Working Group & The Cancer Genome Atlas Research Network lding@wustl.edu, Aug 9 2018, In: Cell. 174, 4, p. 1034-1035 2 p.

  Research output: Contribution to journal › Comment/debate

  Open Access

  • Neoplasm Genes 100%
  • Mutation 77%
  • Adenocarcinoma 72%
  • ethyl-2-methylthio-4-methyl-5-pyrimidine carboxylate 48%
  • Error 34%
  201 Scopus citations

• Erratum: The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma (Cell Reports (2018) 23(1) (313–326.e5) (S2211124718304364) (10.1016/j.celrep.2018.03.075))

  The Cancer Genome Atlas Research Network, Jun 19 2018, In: Cell Reports. 23, 12, p. 3698 1 p.

  Research output: Contribution to journal › Comment/debate

  Open Access

  • Atlases 100%
  • Renal Cell Carcinoma 89%
  • Names 88%
  • Emotions 73%
  • Error 69%
  78 Scopus citations

• Erratum to: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (Nature Communications, (2018), 9, 1, (2606), 10.1038/s41467-018-04668-w)

  NHLBI TOPMed Lipids Working Group, Dec 1 2018, In: Nature communications. 9, 1, 3493.

  Research output: Contribution to journal › Comment/debate

  Open Access

  • document markup languages 100%
  • lipoproteins 81%
  • genome 72%
  • Lipoprotein(a) 68%
  • Lipoprotein 61%
  1 Scopus citations

• Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas

  The Cancer Genome Atlas Research Network, Apr 3 2018, In: Cell Reports. 23, 1, p. 194-212.e6

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Mutation 100%
  • Squamous Cell Carcinoma 98%
  • MicroRNA 96%
  • MicroRNAs 49%
  • Epithelial Cells 42%
  166 Scopus citations

• Genomic and Functional Approaches to Understanding Cancer Aneuploidy

  The Cancer Genome Atlas Research Network, Apr 9 2018, In: Cancer Cell. 33, 4, p. 676-689.e3

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Aneuploidy 100%
  • Chromosomes 55%
  • Neoplasms 29%
  • Mutation Rate 24%
  • Genome 23%
  417 Scopus citations

• Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas

  The Cancer Genome Atlas Research Network, Apr 3 2018, In: Cell Reports. 23, 1, p. 239-254.e6

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • DNA Repair-Deficiency Disorders 100%
  • Atlases 73%
  • DNA Damage 59%
  • Mutation 57%
  • Genome 46%
  482 Scopus citations

• Integrated Genomic Analysis of the Ubiquitin Pathway across Cancer Types

  The Cancer Genome Atlas Research Network, Apr 3 2018, In: Cell Reports. 23, 1, p. 213-226.e3

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Ubiquitin 100%
  • Mutation 42%
  • Protein 41%
  • Molecular Cluster 32%
  • Neoplasms 32%
  62 Scopus citations