Steven McCarroll - Related publications

Harvard Medical School, Boston, MA, United States 
Human genome variation, schizophrenia, and the molecular biology of neurons and microglia
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19 most relevant papers in past 60 days:
Year Citation  Score
2022 Sun Q, Crowley CA, Huang L, Wen J, Chen J, Bao EL, Auer PL, Lettre G, Reiner AP, Sankaran VG, Raffield LM, Li Y. From GWAS variant to function: A study of ∼148,000 variants for blood cell traits. Hgg Advances. 3: 100063. PMID 35047852 DOI: 10.1016/j.xhgg.2021.100063   
2022 Ng JW, Chong ETJ, Lee PC. An Updated Review on the Role of Single Nucleotide Polymorphisms in COVID-19 Disease Severity: A Global Aspect. Current Pharmaceutical Biotechnology. PMID 35034591 DOI: 10.2174/1389201023666220114162347   
2022 Sahajpal NS, Jill Lai CY, Hastie A, Mondal AK, Dehkordi SR, van der Made CI, Fedrigo O, Al-Ajli F, Jalnapurkar S, Byrska-Bishop M, Kanagal-Shamanna R, Levy B, Schieck M, Illig T, Bacanu SA, ... , et al. Optical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19. Iscience. 103760. PMID 35036860 DOI: 10.1016/j.isci.2022.103760   
2022 Restuadi R, Steyn FJ, Kabashi E, Ngo ST, Cheng FF, Nabais MF, Thompson MJ, Qi T, Wu Y, Henders AK, Wallace L, Bye CR, Turner BJ, Ziser L, Mathers S, et al. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1. Genome Medicine. 14: 7. PMID 35042540 DOI: 10.1186/s13073-021-01006-6   
2022 Dennis J, Tyrer JP, Walker LC, Michailidou K, Dorling L, Bolla MK, Wang Q, Ahearn TU, Andrulis IL, Anton-Culver H, Antonenkova NN, Arndt V, Aronson KJ, Freeman LEB, Beckmann MW, ... , ... , ... , ... , et al. Rare germline copy number variants (CNVs) and breast cancer risk. Communications Biology. 5: 65. PMID 35042965 DOI: 10.1038/s42003-021-02990-6   
2022 Null M, Yilmaz F, Astling D, Yu HC, Cole JB, Hallgrímsson B, Santorico SA, Spritz RA, Shaikh TH, Hendricks AE. Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans. Hgg Advances. 3: 100082. PMID 35047866 DOI: 10.1016/j.xhgg.2021.100082   
2022 Breeze CE, Haugen E, Reynolds A, Teschendorff A, van Dongen J, Lan Q, Rothman N, Bourque G, Dunham I, Beck S, Stamatoyannopoulos J, Franceschini N, Berndt SI. Integrative analysis of 3604 GWAS reveals multiple novel cell type-specific regulatory associations. Genome Biology. 23: 13. PMID 34996498 DOI: 10.1186/s13059-021-02560-3   
2022 Ware SM, Bhatnagar S, Dexheimer PJ, Wilkinson JD, Sridhar A, Fan X, Shen Y, Tariq M, Schubert JA, Colan SD, Shi L, Canter CE, Hsu DT, Bansal N, Webber SA, ... , et al. The genetic architecture of pediatric cardiomyopathy. American Journal of Human Genetics. PMID 35026164 DOI: 10.1016/j.ajhg.2021.12.006   
2022 Chen R, Cheng RA, Wiedmann M, Orsi RH. Development of a Genomics-Based Approach To Identify Putative Hypervirulent Nontyphoidal Salmonella Isolates: Salmonella enterica Serovar Saintpaul as a Model. Msphere. e0073021. PMID 34986312 DOI: 10.1128/msphere.00730-21   
2022 Burton AR, Gravem SA, Barreto FS. Little evidence for genetic variation associated with susceptibility to sea star wasting syndrome in the keystone species Pisaster ochraceus. Molecular Ecology. 31: 197-205. PMID 34626020 DOI: 10.1111/mec.16212   
2022 Xia G, Li Y, Pan W, Qian C, Ma L, Zhou J, Xu H, Cheng C. SLAMF6 is associated with the susceptibility and severity of rheumatoid arthritis in the Chinese population. Journal of Orthopaedic Surgery and Research. 17: 13. PMID 35016729 DOI: 10.1186/s13018-021-02901-9   
2022 Kim C, Kim YJ, Choi W, Jang HM, Hwang MY, Jung S, Lim H, Hong SB, Yoon K, Kim BJ, Park HY, Han B. Phenome-wide association study of the major histocompatibility complex region in the Korean population identifies novel association signals. Human Molecular Genetics. PMID 35043955 DOI: 10.1093/hmg/ddac016   
2022 Preston CG, Wright MW, Madhavrao R, Harrison SM, Goldstein JL, Luo X, Wand H, Wulf B, Cheung G, Mandell ME, Tong H, Cheng S, Iacocca MA, Pineda AL, Popejoy AB, ... , et al. ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines. Genome Medicine. 14: 6. PMID 35039090 DOI: 10.1186/s13073-021-01004-8   
2022 Wang Z, Zhou L, Lan Y, Li X, Wang J, Dong J, Guo W, Jing D, Liu Q, Zhang S, Liu Z, Shi W, Yang W, Yang T, Sun F, et al. An aspartic protease 47 causes quantitative recessive resistance to rice black-streaked dwarf virus disease and southern rice black-streaked dwarf virus disease. The New Phytologist. PMID 35015901 DOI: 10.1111/nph.17961   
2022 Zhao Y, Pu Y, Liang B, Bai T, Liu Y, Jiang L, Ma Y. A study using single-locus and multi-locus genome-wide association study to identify genes associated with teat number in Hu sheep. Animal Genetics. PMID 35040155 DOI: 10.1111/age.13169   
2022 Abdelrahman HA, Akawi N, Al-Shamsi AM, Ali A, Al-Jasmi F, John A, Hertecant J, Al-Gazali L, Ali BR. Bi-allelic null variant in matrix metalloproteinase-15, causes congenital cardiac defect, cholestasis jaundice, and failure to thrive. Clinical Genetics. PMID 34988996 DOI: 10.1111/cge.14107   
2022 Kuno A, Ikeda Y, Ayabe S, Kato K, Sakamoto K, Suzuki SR, Morimoto K, Wakimoto A, Mikami N, Ishida M, Iki N, Hamada Y, Takemura M, Daitoku Y, Tanimoto Y, et al. DAJIN enables multiplex genotyping to simultaneously validate intended and unintended target genome editing outcomes. Plos Biology. 20: e3001507. PMID 35041655 DOI: 10.1371/journal.pbio.3001507   
2022 Qi G, Dutta D, Leroux A, Ray D, Muschelli J, Crainiceanu C, Chatterjee N. Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Genetic Epidemiology. PMID 35043453 DOI: 10.1002/gepi.22441   
2022 Zhang S, Cooper-Knock J, Weimer AK, Shi M, Moll T, Marshall JNG, Harvey C, Nezhad HG, Franklin J, Souza CDS, Ning K, Wang C, Li J, Dilliott AA, Farhan S, ... , et al. Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis. Neuron. PMID 35045337 DOI: 10.1016/j.neuron.2021.12.019