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Chaolong Wang, Ph.D. - Publications

Affiliations: 
2012 Bioinformatics University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Genetics, Biostatistics Biology, Bioinformatics Biology
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37 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
2023 Hao X, Shao Z, Zhang N, Jiang M, Cao X, Li S, Guan Y, Wang C. Integrative genome-wide analyses identify novel loci associated with kidney stones and provide insights into its genetic architecture. Nature Communications. 14: 7498. PMID 37980427 DOI: 10.1038/s41467-023-43400-1  0.356
2023 Graham SE, Clarke SL, Wu KH, Kanoni S, Zajac GJM, Ramdas S, Surakka I, Ntalla I, Vedantam S, Winkler TW, Locke AE, Marouli E, Hwang MY, Han S, Narita A, ... ... Wang C, ... ... Wang CA, et al. Author Correction: The power of genetic diversity in genome-wide association studies of lipids. Nature. PMID 37237109 DOI: 10.1038/s41586-023-06194-2  0.506
2022 Kanoni S, Graham SE, Wang Y, Surakka I, Ramdas S, Zhu X, Clarke SL, Bhatti KF, Vedantam S, Winkler TW, Locke AE, Marouli E, Zajac GJM, Wu KH, Ntalla I, ... ... Wang C, ... ... Wang CA, et al. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome Biology. 23: 268. PMID 36575460 DOI: 10.1186/s13059-022-02837-1  0.635
2022 Yengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, Sakaue S, Graff M, Eliasen AU, Jiang Y, Raghavan S, Miao J, Arias JD, Graham SE, Mukamel RE, Spracklen CN, ... ... Wang CA, ... ... Wang C, et al. A saturated map of common genetic variants associated with human height. Nature. PMID 36224396 DOI: 10.1038/s41586-022-05275-y  0.536
2022 Ramdas S, Judd J, Graham SE, Kanoni S, Wang Y, Surakka I, Wenz B, Clarke SL, Chesi A, Wells A, Bhatti KF, Vedantam S, Winkler TW, Locke AE, Marouli E, ... ... Wang C, ... ... Wang CA, et al. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids. American Journal of Human Genetics. 109: 1366-1387. PMID 35931049 DOI: 10.1016/j.ajhg.2022.06.012  0.514
2022 Winkler TW, Rasheed H, Teumer A, Gorski M, Rowan BX, Stanzick KJ, Thomas LF, Tin A, Hoppmann A, Chu AY, Tayo B, Thio CHL, Cusi D, Chai JF, Sieber KB, ... ... Wang C, et al. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals. Communications Biology. 5: 580. PMID 35697829 DOI: 10.1038/s42003-022-03448-z  0.645
2021 Graham SE, Clarke SL, Wu KH, Kanoni S, Zajac GJM, Ramdas S, Surakka I, Ntalla I, Vedantam S, Winkler TW, Locke AE, Marouli E, Hwang MY, Han S, Narita A, ... ... Wang C, ... ... Wang CA, et al. The power of genetic diversity in genome-wide association studies of lipids. Nature. PMID 34887591 DOI: 10.1038/s41586-021-04064-3  0.556
2021 Chen J, Spracklen CN, Marenne G, Varshney A, Corbin LJ, Luan J, Willems SM, Wu Y, Zhang X, Horikoshi M, Boutin TS, Mägi R, Waage J, Li-Gao R, Chan KHK, ... ... Wang CA, ... ... Wang C, et al. The trans-ancestral genomic architecture of glycemic traits. Nature Genetics. PMID 34059833 DOI: 10.1038/s41588-021-00852-9  0.653
2020 Chai JF, Kao SL, Wang C, Lim VJ, Khor IW, Dou J, Podgornaia AI, Chothani S, Cheng CY, Sabanayagam C, Wong TY, van Dam RM, Liu J, Reilly DF, Paterson AD, et al. Genome-wide association for HbA1c in Malay identified deletion on SLC4A1 that influences HbA1c independent of glycemia. The Journal of Clinical Endocrinology and Metabolism. PMID 32936915 DOI: 10.1210/Clinem/Dgaa658  0.429
2020 Hao X, Wang K, Dai C, Ding Z, Yang W, Wang C, Cheng S. Integrative Analysis of scRNA-seq and GWAS Data Pinpoints Periportal Hepatocytes as the Relevant Liver Cell Types for Blood Lipids. Human Molecular Genetics. PMID 32821946 DOI: 10.1093/Hmg/Ddaa188  0.328
2020 Dou J, Wu D, Ding L, Wang K, Jiang M, Chai X, Reilly DF, Tai ES, Liu J, Sim X, Cheng S, Wang C. Using off-target data from whole-exome sequencing to improve genotyping accuracy, association analysis and polygenic risk prediction. Briefings in Bioinformatics. PMID 32591784 DOI: 10.1093/Bib/Bbaa084  0.406
2020 Leong A, Lim VJY, Wang C, Chai JF, Dorajoo R, Heng CK, van Dam RM, Koh WP, Yuan JM, Jonas JB, Wang YX, Wei WB, Liu J, Reilly DF, Wong TY, et al. Association of variants with hemoglobin A1c and impact on diabetes diagnosis in East Asian individuals. Bmj Open Diabetes Research & Care. 8. PMID 32209585 DOI: 10.1136/Bmjdrc-2019-001091  0.367
2019 Wu D, Dou J, Chai X, Bellis C, Wilm A, Shih CC, Soon WWJ, Bertin N, Lin CB, Khor CC, DeGiorgio M, Cheng S, Bao L, Karnani N, Hwang WYK, ... ... Wang C, et al. Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore. Cell. 179: 736-749.e15. PMID 31626772 DOI: 10.1016/J.Cell.2019.09.019  0.427
2019 Teumer A, Li Y, Ghasemi S, Prins BP, Wuttke M, Hermle T, Giri A, Sieber KB, Qiu C, Kirsten H, Tin A, Chu AY, Bansal N, Feitosa MF, Wang L, ... ... Wang C, et al. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Nature Communications. 10: 4130. PMID 31511532 DOI: 10.1038/S41467-019-11576-0  0.434
2019 Wuttke M, Li Y, Li M, Sieber KB, Feitosa MF, Gorski M, Tin A, Wang L, Chu AY, Hoppmann A, Kirsten H, Giri A, Chai JF, Sveinbjornsson G, Tayo BO, ... ... Wang C, et al. A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nature Genetics. 51: 957-972. PMID 31152163 DOI: 10.1038/s41588-019-0407-x  0.64
2018 Chen H, Huffman JE, Brody JA, Wang C, Lee S, Li Z, Gogarten SM, Sofer T, Bielak LF, Bis JC, Blangero J, Bowler RP, Cade BE, Cho MH, Correa A, et al. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. American Journal of Human Genetics. PMID 30639324 DOI: 10.1016/J.Ajhg.2018.12.012  0.399
2018 Takeuchi F, Akiyama M, Matoba N, Katsuya T, Nakatochi M, Tabara Y, Narita A, Saw WY, Moon S, Spracklen CN, Chai JF, Kim YJ, Zhang L, Wang C, Li H, et al. Interethnic analyses of blood pressure loci in populations of East Asian and European descent. Nature Communications. 9: 5052. PMID 30487518 DOI: 10.1038/S41467-018-07345-0  0.353
2017 Chen H, Cade BE, Gleason KJ, Bjonnes AC, Stilp AM, Sofer T, Conomos MP, Ancoli-Israel S, Arens R, Azarbarzin A, Bell GI, Below JE, Chun S, Evans DS, Ewert R, ... ... Wang C, et al. Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men. American Journal of Respiratory Cell and Molecular Biology. PMID 29077507 DOI: 10.1165/Rcmb.2017-0237Oc  0.373
2017 Liu J, Wan X, Wang C, Yang C, Zhou X, Yang C. LLR: A latent low-rank approach to colocalizing genetic risk variants in multiple GWAS. Bioinformatics (Oxford, England). PMID 28961754 DOI: 10.1093/Bioinformatics/Btx512  0.43
2017 Dou J, Sun B, Sim X, Hughes JD, Reilly DF, Tai ES, Liu J, Wang C. Estimation of kinship coefficient in structured and admixed populations using sparse sequencing data. Plos Genetics. 13: e1007021. PMID 28961250 DOI: 10.1371/Journal.Pgen.1007021  0.389
2017 Liu H, Wang Z, Li Y, Yu G, Fu X, Wang C, Liu W, Yu Y, Bao F, Irwanto A, Liu J, Chu T, Andiappan AK, Maurer-Stroh S, Limviphuvadh V, ... ... Wang C, et al. Genome-wide Analysis of Protein-Coding Variants in Leprosy. The Journal of Investigative Dermatology. PMID 28842327 DOI: 10.1016/J.Jid.2017.08.004  0.323
2017 Wang Z, Henn BC, Wang C, Wei Y, Su L, Sun R, Chen H, Wagner PJ, Lu Q, Lin X, Wright R, Bellinger D, Kile M, Mazumdar M, Tellez-Rojo MM, et al. Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment. Environmental Health : a Global Access Science Source. 16: 81. PMID 28754176 DOI: 10.1186/S12940-017-0288-3  0.356
2017 Dai W, Yang M, Wang C, Cai T. Sequence robust association test for familial data. Biometrics. PMID 28273695 DOI: 10.1111/Biom.12643  0.395
2017 Taliun D, Chothani S, Schönherr S, Forer L, Boehnke M, Abecasis GR, Wang C. LASER server: ancestry tracing with genotypes or sequence reads. Bioinformatics (Oxford, England). PMID 28200055 DOI: 10.1093/Bioinformatics/Btx075  0.49
2016 Wang X, Zhang Z, Morris N, Cai T, Lee S, Wang C, Yu TW, Walsh CA, Lin X. Rare variant association test in family-based sequencing studies. Briefings in Bioinformatics. PMID 27677958 DOI: 10.1093/Bib/Bbw083  0.373
2016 Chen H, Wang C, Conomos MP, Stilp AM, Li Z, Sofer T, Szpiro AA, Chen W, Brehm JM, Celedón JC, Redline S, Papanicolaou GJ, Thornton TA, Laurie CC, Rice K, et al. Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models. American Journal of Human Genetics. PMID 27018471 DOI: 10.1016/J.Ajhg.2016.02.012  0.422
2016 Cade BE, Chen H, Stilp AM, Gleason KJ, Sofer T, Ancoli-Israel S, Arens R, Bell GI, Below JE, Bjonnes AC, Chun S, Conomos MP, Evans DS, Johnson WC, Frazier-Wood AC, ... ... Wang C, et al. Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans. American Journal of Respiratory and Critical Care Medicine. PMID 26977737 DOI: 10.1164/Rccm.201512-2431Oc  0.338
2015 Lin X, Lee S, Wu MC, Wang C, Chen H, Li Z, Lin X. Test for rare variants by environment interactions in sequencing association studies. Biometrics. PMID 26229047 DOI: 10.1111/Biom.12368  0.337
2015 Wang C, Zhan X, Liang L, Abecasis GR, Lin X. Improved ancestry estimation for both genotyping and sequencing data using projection procrustes analysis and genotype imputation. American Journal of Human Genetics. 96: 926-37. PMID 26027497 DOI: 10.1016/J.Ajhg.2015.04.018  0.401
2014 Wang C, Zhan X, Bragg-Gresham J, Kang HM, Stambolian D, Chew EY, Branham KE, Heckenlively J, Fulton R, Wilson RK, Mardis ER, Lin X, Swaroop A, Zöllner S, Abecasis GR. Ancestry estimation and control of population stratification for sequence-based association studies Nature Genetics. 46: 409-415. PMID 24633160 DOI: 10.1038/Ng.2924  0.394
2013 Zhan X, Larson DE, Wang C, Koboldt DC, Sergeev YV, Fulton RS, Fulton LL, Fronick CC, Branham KE, Bragg-Gresham J, Jun G, Hu Y, Kang HM, Liu D, Othman M, et al. Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nature Genetics. 45: 1375-9. PMID 24036949 DOI: 10.1038/Ng.2758  0.328
2012 Wang C, Zöllner S, Rosenberg NA. A quantitative comparison of the similarity between genes and geography in worldwide human populations. Plos Genetics. 8: e1002886. PMID 22927824 DOI: 10.1371/Journal.Pgen.1002886  0.408
2012 Wang C, Schroeder KB, Rosenberg NA. A maximum-likelihood method to correct for allelic dropout in microsatellite data with no replicate genotypes. Genetics. 192: 651-69. PMID 22851645 DOI: 10.1534/Genetics.112.139519  0.349
2010 Pemberton TJ, Wang C, Li JZ, Rosenberg NA. Inference of unexpected genetic relatedness among individuals in HapMap Phase III. American Journal of Human Genetics. 87: 457-64. PMID 20869033 DOI: 10.1016/J.Ajhg.2010.08.014  0.371
2010 Wang C, Szpiech ZA, Degnan JH, Jakobsson M, Pemberton TJ, Hardy JA, Singleton AB, Rosenberg NA. Comparing spatial maps of human population-genetic variation using Procrustes analysis. Statistical Applications in Genetics and Molecular Biology. 9: Article 13. PMID 20196748 DOI: 10.2202/1544-6115.1493  0.379
2009 Kopelman NM, Stone L, Wang C, Gefel D, Feldman MW, Hillel J, Rosenberg NA. Genomic microsatellites identify shared Jewish ancestry intermediate between Middle Eastern and European populations. Bmc Genetics. 10: 80. PMID 19995433 DOI: 10.1186/1471-2156-10-80  0.347
2009 Huang L, Wang C, Rosenberg NA. The relationship between imputation error and statistical power in genetic association studies in diverse populations. American Journal of Human Genetics. 85: 692-8. PMID 19853241 DOI: 10.1016/J.Ajhg.2009.09.017  0.366
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