Peter Crane, Ph.D - Related publications

Affiliations: 
Yale University, New Haven, CT 
Area:
Paleobotany
NOTE: We are testing a new system for identifying relevant work based on semantic analysis that identifies similarities between recently published papers and the current author's publications. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches.
50 most relevant papers in past 60 days:
Year Citation  Score
2021 Akinyemi RO, Yaria J, Ojagbemi A, Guerchet M, Okubadejo N, Njamnshi AK, Sarfo FS, Akpalu A, Ogbole G, Ayantayo T, Adokonou T, Paddick SM, Ndetei D, Bosche J, Ayele B, ... , et al. Dementia in Africa: Current evidence, knowledge gaps, and future directions. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 34569714 DOI: 10.1002/alz.12432   
2021 Li Y, Xiao FL, Cheng H, Liang B, Zhou FS, Li P, Zheng XD, Sun LD, Yang S, Zhang XJ. A Common Variant in 11q23.3 Is Associated with Susceptibility to Atopic Dermatitis in the Han Chinese Population. Genetic Testing and Molecular Biomarkers. PMID 34609929 DOI: 10.1089/gtmb.2020.0335   
2021 Das S, Pearson M, Taylor K, Bouchet V, Møller GL, Hall TO, Strivens M, Tzeng KTH, Gardner S. Combinatorial Analysis of Phenotypic and Clinical Risk Factors Associated With Hospitalized COVID-19 Patients. Frontiers in Digital Health. 3: 660809. PMID 34713134 DOI: 10.3389/fdgth.2021.660809   
2021 Verma A, Tsao NL, Thomann L, Ho YL, Iyengar SK, Luoh SW, Carr R, Crawford D, Efird JT, Huffman J, Hung A, Ivey KL, Levin M, Lynch J, Natarajan P, ... , et al. A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program. Medrxiv : the Preprint Server For Health Sciences. PMID 34642702 DOI: 10.1101/2021.05.18.21257396   
2021 Nalls MA, Blauwendraat C, Sargent L, Vitale D, Leonard H, Iwaki H, Song Y, Bandres-Ciga S, Menden K, Faghri F, Heutink P, Cookson MR, Singleton AB. Evidence for connecting multiple neurodegenerative diseases. Brain Communications. 3: fcab095. PMID 34693284 DOI: 10.1093/braincomms/fcab095   
2021 Wang Z, Zhang Q, Lin JR, Jabalameli MR, Mitra J, Nguyen N, Zhang ZD. Deep post-GWAS analysis identifies potential risk genes and risk variants for Alzheimer's disease, providing new insights into its disease mechanisms. Scientific Reports. 11: 20511. PMID 34654853 DOI: 10.1038/s41598-021-99352-3   
2021 Xin XY, Lai ZH, Ding KQ, Zeng LL, Ma JF. Angiotensin-converting enzyme polymorphisms AND Alzheimer's disease susceptibility: An updated meta-analysis. Plos One. 16: e0260498. PMID 34818351 DOI: 10.1371/journal.pone.0260498   
2021 Zazuli Z, de Jong C, Xu W, Vijverberg SJH, Masereeuw R, Patel D, Mirshams M, Khan K, Cheng D, Ordonez-Perez B, Huang S, Spreafico A, Hansen AR, Goldstein DP, de Almeida JR, et al. Association between Genetic Variants and Cisplatin-Induced Nephrotoxicity: A Genome-Wide Approach and Validation Study. Journal of Personalized Medicine. 11. PMID 34834585 DOI: 10.3390/jpm11111233   
2021 Zheng J, Wu YY, Fang WL, Cai XY, Zhang ZY, Yu CX, Zheng XD, Xiao FL. Confirming the TMEM232 gene associated with atopic dermatitis through targeted capture sequencing. Scientific Reports. 11: 21830. PMID 34750414 DOI: 10.1038/s41598-021-01194-6   
2021 Dilliott AA, Abdelhady A, Sunderland KM, Farhan SMK, Abrahao A, Binns MA, Black SE, Borrie M, Casaubon LK, Dowlatshahi D, Finger E, Fischer CE, Frank A, Freedman M, Grimes D, ... , et al. Contribution of rare variant associations to neurodegenerative disease presentation. Npj Genomic Medicine. 6: 80. PMID 34584092 DOI: 10.1038/s41525-021-00243-3   
2021 Lord J, Zettergren A, Ashton NJ, Karikari TK, Benedet AL, Simrén J, , Hye A, Aarsland D, , Blennow K, Zetterberg H, Proitsi P. A genome-wide association study of plasma phosphorylated tau181. Neurobiology of Aging. 106: 304.e1-304.e3. PMID 34119372 DOI: 10.1016/j.neurobiolaging.2021.04.018   
2021 Prakrithi P, Lakra P, Sundar D, Kapoor M, Mukerji M, Gupta I, The Indian Genome Variation Consortium. Genetic Risk Prediction of COVID-19 Susceptibility and Severity in the Indian Population. Frontiers in Genetics. 12: 714185. PMID 34707636 DOI: 10.3389/fgene.2021.714185   
2021 Wojczynski MK, Lin SJ, Sebastiani P, Perls TT, Lee J, Kulminski A, Newman A, Zmuda JM, Christensen K, Province MA. NIA Long Life Family Study: Objectives, Design, and Heritability of Cross Sectional and Longitudinal Phenotypes. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 34739053 DOI: 10.1093/gerona/glab333   
2021 Wojczynski MK, Lin SJ, Sebastiani P, Perls TT, Lee J, Kulminski A, Newman A, Zmuda JM, Christensen K, Province MA. NIA Long Life Family Study: Objectives, Design, and Heritability of Cross Sectional and Longitudinal Phenotypes. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 34739053 DOI: 10.1093/gerona/glab333   
2021 Barowsky S, Jung JY, Nesbit N, Silberstein M, Fava M, Loggia ML, Smoller JW, Lee PH. Cross-Disorder Genomics Data Analysis Elucidates a Shared Genetic Basis Between Major Depression and Osteoarthritis Pain. Frontiers in Genetics. 12: 687687. PMID 34603368 DOI: 10.3389/fgene.2021.687687   
2021 Zhu H, Zheng F, Li L, Jin Y, Luo Y, Li Z, Zeng J, Tang L, Li Z, Xia N, Liu P, Han D, Shan Y, Zhu X, Liu S, et al. A Chinese host genetic study discovered IFNs and causality of laboratory traits on COVID-19 severity. Iscience. 103186. PMID 34608450 DOI: 10.1016/j.isci.2021.103186   
2021 Yang Y, Li D, He C, Peng L, Xing S, Bai M, Rong H, Yuan D, He Y, He X, Wang L, Jin T. Fc receptor-like 1, 3, and 6 variants are associated with rheumatoid arthritis risk in the Chinese Han population. Genes and Environment : the Official Journal of the Japanese Environmental Mutagen Society. 43: 42. PMID 34620245 DOI: 10.1186/s41021-021-00213-2   
2021 Rohde PD, Nyegaard M, Kjolby M, Sørensen P. Multi-Trait Genomic Risk Stratification for Type 2 Diabetes. Frontiers in Medicine. 8: 711208. PMID 34568370 DOI: 10.3389/fmed.2021.711208   
2021 Backman JD, Li AH, Marcketta A, Sun D, Mbatchou J, Kessler MD, Benner C, Liu D, Locke AE, Balasubramanian S, Yadav A, Banerjee N, Gillies C, Damask A, Liu S, ... , ... , et al. Exome sequencing and analysis of 454,787 UK Biobank participants. Nature. PMID 34662886 DOI: 10.1038/s41586-021-04103-z   
2021 Prince C, Mitchell RE, Richardson TG. Integrative multiomics analysis highlights immune-cell regulatory mechanisms and shared genetic architecture for 14 immune-associated diseases and cancer outcomes. American Journal of Human Genetics. PMID 34741802 DOI: 10.1016/j.ajhg.2021.10.003   
2021 Lali R, Chong M, Omidi A, Mohammadi-Shemirani P, Le A, Cui E, Paré G. Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories. Nature Communications. 12: 5852. PMID 34615865 DOI: 10.1038/s41467-021-26114-0   
2021 Hsiao YJ, Chuang HK, Chi SC, Wang YY, Chiang PH, Teng PC, Kuang TM, Yarmishyn AA, Lin TC, Hwang DK, Chen SJ, Chiou SH, Chen MJ, Hsieh AR, Hsu CC. Genome-Wide Polygenic Risk Score for Predicting High Risk Glaucoma Individuals of Han Chinese Ancestry. Journal of Personalized Medicine. 11. PMID 34834521 DOI: 10.3390/jpm11111169   
2021 Faruq RN, D'Silva P, Lau FD, Zhao C, Majumdar S. Early-Onset Vascular Dementia in a 43-Year-Old Man with Accelerated Atherosclerotic Disease, Elevated Lipoprotein (a), and a Missense DNAJC5 Variant with Potential Association to Adult-Onset Ceroid Lipofuscinosis. Case Reports in Neurology. 13: 565-571. PMID 34720963 DOI: 10.1159/000518194   
2021 Ritchie SC, Lambert SA, Arnold M, Teo SM, Lim S, Scepanovic P, Marten J, Zahid S, Chaffin M, Liu Y, Abraham G, Ouwehand WH, Roberts DJ, Watkins NA, Drew BG, et al. Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases. Nature Metabolism. PMID 34750571 DOI: 10.1038/s42255-021-00478-5   
2021 Xie Y, Li M, Dong W, Jiang W, Zhao H. M-DATA: A statistical approach to jointly analyzing de novo mutations for multiple traits. Plos Genetics. 17: e1009849. PMID 34735430 DOI: 10.1371/journal.pgen.1009849   
2021 Polfus LM, Darst BF, Highland H, Sheng X, Ng MCY, Below JE, Petty L, Bien S, Sim X, Wang W, Fontanillas P, Patel Y, , , , et al. Genetic discovery and risk characterization in type 2 diabetes across diverse populations. Hgg Advances. 2. PMID 34604815 DOI: 10.1016/j.xhgg.2021.100029   
2021 Venkataraman GR, DeBoever C, Tanigawa Y, Aguirre M, Ioannidis AG, Mostafavi H, Spencer CCA, Poterba T, Bustamante CD, Daly MJ, Pirinen M, Rivas MA. Bayesian model comparison for rare-variant association studies. American Journal of Human Genetics. PMID 34822764 DOI: 10.1016/j.ajhg.2021.11.005   
2021 Belbin GM, Rutledge S, Dodatko T, Cullina S, Turchin MC, Kohli S, Torre D, Yee MC, Gignoux CR, Abul-Husn NS, Houten SM, Kenny EE. Leveraging health systems data to characterize a large effect variant conferring risk for liver disease in Puerto Ricans. American Journal of Human Genetics. PMID 34678161 DOI: 10.1016/j.ajhg.2021.09.016   
2021 Freitas AT, Calhau C, Antunes G, Araújo B, Bandeira M, Barreira S, Bazenga F, Braz S, Caldeira D, Santos SCR, Faria A, Faria D, Fraga M, Nogueira-Garcia B, Gonçalves L, et al. Vitamin D-related polymorphisms and vitamin D levels as risk biomarkers of COVID-19 disease severity. Scientific Reports. 11: 20837. PMID 34675344 DOI: 10.1038/s41598-021-99952-z   
2021 Katz DH, Tahir UA, Bick AG, Pampana A, Ngo D, Benson MD, Yu Z, Robbins JM, Chen ZZ, Cruz DE, Deng S, Farrell L, Sinha S, Schmaier AA, Shen D, ... , et al. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights into Cardiovascular Disease. Circulation. PMID 34814699 DOI: 10.1161/CIRCULATIONAHA.121.055117   
2021 Zhang T, Wei H, Li M, Han W, Zhang W, Zhang X, Zhang B, Jiang Z, Li T. Risk of migraine contributed by genetic polymorphisms of ANKDD1B gene: a case-control study based on Chinese Han population. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 34669083 DOI: 10.1007/s10072-021-05645-w   
2021 Barbier M, Camuzat A, Hachimi KE, Guegan J, Rinaldi D, Lattante S, Houot M, Sánchez-Valle R, Sabatelli M, Antonell A, Molina-Porcel L, Clot F, Couratier P, van der Ende E, van der Zee J, ... , et al. SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration. Brain : a Journal of Neurology. 144: 2798-2811. PMID 34687211 DOI: 10.1093/brain/awab171   
2021 Wang Y, Zhu X, Chen Z, Yang P, Liu L, Liu X, Wu L, He Q, Li Y. Natural histories of metabolite BMI phenotypes and their impacts on cardiovascular disease risk over a decade-long follow-up. Obesity Research & Clinical Practice. 15: 579-586. PMID 34742668 DOI: 10.1016/j.orcp.2021.10.002   
2021 Cao Z, Huang Y, Duan R, Jin P, Qin ZS, Zhang S. Disease category-specific annotation of variants using an ensemble learning framework. Briefings in Bioinformatics. PMID 34643213 DOI: 10.1093/bib/bbab438   
2021 Vu NT, Phuc TH, Oanh KTP, Sang NV, Trang TT, Nguyen NH. Accuracies of genomic predictions for disease resistance of striped catfish to Edwardsiella ictaluri using artificial intelligence algorithms. G3 (Bethesda, Md.). PMID 34788431 DOI: 10.1093/g3journal/jkab361   
2021 Sakaue S, Kanai M, Tanigawa Y, Karjalainen J, Kurki M, Koshiba S, Narita A, Konuma T, Yamamoto K, Akiyama M, Ishigaki K, Suzuki A, Suzuki K, Obara W, Yamaji K, ... , et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics. 53: 1415-1424. PMID 34594039 DOI: 10.1038/s41588-021-00931-x   
2021 Roy J, Shaikh TM, Del Río Mendoza L, Hosain S, Chapara V, Rahman M. Genome-wide association mapping and genomic prediction for adult stage sclerotinia stem rot resistance in Brassica napus (L) under field environments. Scientific Reports. 11: 21773. PMID 34741104 DOI: 10.1038/s41598-021-01272-9   
2021 Haydock L, Garneau AP, Tremblay L, Yen HY, Gao H, Harrisson R, Isenring P. Genetic abnormalities in biopsy-proven, adult-onset hemolytic uremic syndrome and C3 glomerulopathy. Journal of Molecular Medicine (Berlin, Germany). PMID 34714369 DOI: 10.1007/s00109-021-02102-1   
2021 Kozin MS, Kiselev IS, Baulina NM, Pavlova GV, Boyko AN, Kulakova OG, Favorova OO. [Risk of Multiple Sclerosis: Analysis of Interactions Between Variants of Nuclear and Mitochondrial Genomes]. Molekuliarnaia Biologiia. 55: 956-964. PMID 34837699 DOI: 10.31857/S0026898421060070   
2021 Tran NK, Lea RA, Holland S, Nguyen Q, Raghubar AM, Sutherland HG, Benton MC, Haupt LM, Blackburn NB, Curran JE, Blangero J, Mallett AJ, Griffiths LR. Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease. Scientific Reports. 11: 19425. PMID 34593906 DOI: 10.1038/s41598-021-98935-4   
2021 Lencz T, Backenroth D, Granot-Hershkovitz E, Green A, Gettler K, Cho JH, Weissbrod O, Zuk O, Carmi S. Utility of polygenic embryo screening for disease depends on the selection strategy. Elife. 10. PMID 34635206 DOI: 10.7554/eLife.64716   
2021 Ahmed H, Alarabi L, El-Sappagh S, Soliman H, Elmogy M. Genetic variations analysis for complex brain disease diagnosis using machine learning techniques: opportunities and hurdles. Peerj. Computer Science. 7: e697. PMID 34616886 DOI: 10.7717/peerj-cs.697   
2021 Xhaard C, Rouget R, Vodovar N, Le Floch E, Dandine-Roulland C, Wagner S, Bacq-Daian D, Thuillier Q, Boivin JM, Branlant C, Deleuze JF, Behm-Ansmant I, Zannad F, Rossignol P, Girerd N. Impact of natriuretic peptide polymorphisms on diastolic and metabolic function in a populational cohort: insights from the STANISLAS cohort. Esc Heart Failure. PMID 34734498 DOI: 10.1002/ehf2.13674   
2021 Kurul SH, Oktay Y, Töpf A, Szabó NZ, Güngör S, Yaramis A, Sonmezler E, Matalonga L, Yis U, Schon K, Paramonov I, Kalafatcilar İP, Gao F, Rieger A, Arslan N, ... , et al. High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases. Brain : a Journal of Neurology. PMID 34791078 DOI: 10.1093/brain/awab395   
2021 Mkaouar R, Riahi Z, Charfeddine C, Chelly I, Boudabbous H, Dallali H, Bonnet C, Hechmi M, Bekri S, Zitouna N, Zekri L, Tounsi A, Kefi R, Marrakchi J, Messaoud O, et al. Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment. Plos One. 16: e0258202. PMID 34614013 DOI: 10.1371/journal.pone.0258202   
2021 Chen T, Lin YX, Zha Y, Sun Y, Tian J, Yang Z, Lin SW, Yu F, Chen ZS, Kuang BH, Lei JJ, Nie YJ, Xu Y, Tian DB, Li YZ, et al. A Low-Producing Haplotype of Interleukin-6 Disrupting CTCF Binding Is Protective against Severe COVID-19. Mbio. e0137221. PMID 34634929 DOI: 10.1128/mBio.01372-21   
2021 Melas M, Mathew MT, Mori M, Jayaraman V, Wilson SA, Martin C, Jacobson-Kelly AE, Kelly BJ, Magrini V, Mardis ER, Cottrell CE, Lee K. Somatic Variation as an Incidental Finding in the Pediatric Next Generation Sequencing Era. Cold Spring Harbor Molecular Case Studies. PMID 34716204 DOI: 10.1101/mcs.a006135   
2021 Park JS, Kim Y, Kang J. Genome-wide meta-analysis revealed several genetic loci associated with serum uric acid levels in Korean population: an analysis of Korea Biobank data. Journal of Human Genetics. PMID 34719683 DOI: 10.1038/s10038-021-00991-1   
2021 Adikusuma W, Irham LM, Chou WH, Wong HS, Mugiyanto E, Ting J, Perwitasari DA, Chang WP, Chang WC. Drug Repurposing for Atopic Dermatitis by Integration of Gene Networking and Genomic Information. Frontiers in Immunology. 12: 724277. PMID 34721386 DOI: 10.3389/fimmu.2021.724277   
2021 Shen X, Wen Y, Cui Y, Lu Q. A conditional autoregressive model for genetic association analysis accounting for genetic heterogeneity. Statistics in Medicine. PMID 34811777 DOI: 10.1002/sim.9257