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Search life-sciences literature (45,100,050 articles, preprints and more)

Suggested authors matching "AUTH:Chaffin M" with an ORCID

Mark Chaffin
Geoergia State University
40
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1,544
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Rare variant contribution to the heritability of coronary artery disease.
Rocheleau G, Clarke SL, Auguste G, Hasbani NR, Morrison AC, Heath AS, Bielak LF, Iyer KR, Young EP, Stitziel NO, Jun G, Laurie C, Broome JG, Khan AT, Arnett DK, Becker LC, Bis JC, Boerwinkle E, Bowden DW, [...] Do R
Nat Commun, 15(1):8741, 09 Oct 2024
Cited by: 0 articles | PMID: 39384761 | PMCID: PMC11464707
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Rare coding variant analysis for human diseases across biobanks and ancestries.
Jurgens SJ, Wang X, Choi SH, Weng LC, Koyama S, Pirruccello JP, Nguyen T, Smadbeck P, Jang D, Chaffin M, Walsh R, Roselli C, Elliott AL, Wijdeveld LFJM, Biddinger KJ, Kany S, Rämö JT, Natarajan P, Aragam KG, [...] Ellinor PT
Nat Genet, 56(9):1811-1820, 29 Aug 2024
Cited by: 1 article | PMID: 39210047
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Martian atmospheric hydrogen and deuterium: Seasonal changes and paradigm for escape to space.
Clarke JT, Mayyasi M, Bhattacharyya D, Chaufray JY, Schneider N, Jakosky B, Yelle R, Montmessin F, Chaffin M, Curry S, Deighan J, Jain S, Bertaux JL, Cangi E, Crismani M, Evans S, Gupta S, Lefevre F, Holsclaw G, [...] Elrod M
Sci Adv, 10(30):eadm7499, 26 Jul 2024
Cited by: 0 articles | PMID: 39058782 | PMCID: PMC11277398
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Venus water loss is dominated by HCO⁺ dissociative recombination.
Chaffin MS, Cangi EM, Gregory BS, Yelle RV, Deighan J, Elliott RD, Gröller H
Nature, 629(8011):307-310, 06 May 2024
Cited by: 1 article | PMID: 38710931
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Distinct Plasma Extracellular Vesicle Transcriptomes in Acute Decompensated Heart Failure Subtypes: A Liquid Biopsy Approach.
Gokulnath P, Spanos M, Lehmann HI, Sheng Q, Rodosthenous R, Chaffin M, Varrias D, Chatterjee E, Hutchins E, Li G, Daaboul G, Rana F, Wang AM, Van Keuren-Jensen K, Ellinor PT, Shah R, Das S
Circulation, 149(14):1147-1149, 01 Apr 2024
Cited by: 2 articles | PMID: 38557125
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Transcriptional profile of the rat cardiovascular system at single cell resolution
Arduini A, Fleming SJ, Xiao L, Hall AW, Akkad A, Chaffin M, Bendinelli KJ, Tucker NR, Papangeli I, Mantineo H, Babadi M, Stegmann CM, García-Cardeña G, Lindsay ME, Klattenhoff C, Ellinor PT
bioRxiv, 16 Nov 2023
Cited by: 0 articles | PPR: PPR760206
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Mapping the aetiological foundations of the heart failure spectrum using human genetics
Henry A, Mo X, Finan C, Chaffin MD, Speed D, Issa H, Denaxas S, Ware JS, Zheng SL, Malarstig A, Gratton J, Bond I, Roselli C, Miller D, Chopade S, Schmidt AF, Abner E, Adams L, Andersson C, [...] HERMES Consortium
medRxiv, 03 Oct 2023
Cited by: 0 articles | PPR: PPR735246
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Common and Rare Variant Contributions to Bradyarrhythmias from Multi-Ancestry Meta-Analyses
Weng L, Rämö JT, Jurgens SJ, Khurshid S, Chaffin M, Hall AW, Morrill VN, Nauffal V, Sun YV, Beer D, Lee S, Nadkarni G, Duong T, Wang B, Czuba T, Austin TR, Yoneda ZT, Friedman DJ, Clayton A, [...] Lubitz SA
medRxiv, 25 Sep 2023
Cited by: 0 articles | PPR: PPR729921
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Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma.
Recto K, Kachroo P, Huan T, Van Den Berg D, Lee GY, Bui H, Lee DH, Gereige J, Yao C, Hwang SJ, Joehanes R, Weiss ST, NHLBI Trans-Omics in Precision Medicine (TOPMed) Consortium, O'Connor GT, Levy D, DeMeo DL
EBioMedicine, 95:104758, 18 Aug 2023
Cited by: 1 article | PMID: 37598461 | PMCID: PMC10462855
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Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender.
Fleming SJ, Chaffin MD, Arduini A, Akkad AD, Banks E, Marioni JC, Philippakis AA, Ellinor PT, Babadi M
Nat Methods, 20(9):1323-1335, 07 Aug 2023
Cited by: 132 articles | PMID: 37550580
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Author Correction: Clonal haematopoiesis and risk of chronic liver disease.
Wong WJ, Emdin C, Bick AG, Zekavat SM, Niroula A, Pirruccello JP, Dichtel L, Griffin G, Uddin MM, Gibson CJ, Kovalcik V, Lin AE, McConkey ME, Vromman A, Sellar RS, Kim PG, Agrawal M, Weinstock J, Long MT, [...] Natarajan P
Nature, 619(7970):E47, 01 Jul 2023
Cited by: 0 articles | PMID: 37400552
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Transfer learning enables predictions in network biology.
Theodoris CV, Xiao L, Chopra A, Chaffin MD, Al Sayed ZR, Hill MC, Mantineo H, Brydon EM, Zeng Z, Liu XS, Ellinor PT
Nature, 618(7965):616-624, 31 May 2023
Cited by: 105 articles | PMID: 37258680 | PMCID: PMC10949956
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Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Weinstock JS, Gopakumar J, Burugula BB, Uddin MM, Jahn N, Belk JA, Bouzid H, Daniel B, Miao Z, Ly N, Mack TM, Luna SE, Prothro KP, Mitchell SR, Laurie CA, Broome JG, Taylor KD, Guo X, Sinner MF, [...] Jaiswal S
Nature, 616(7958):755-763, 12 Apr 2023
Cited by: 29 articles | PMID: 37046083 | PMCID: PMC10360040
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Adjusting for common variant polygenic scores improves yield in rare variant association analyses.
Jurgens SJ, Pirruccello JP, Choi SH, Morrill VN, Chaffin M, Lubitz SA, Lunetta KL, Ellinor PT
Nat Genet, 55(4):544-548, 23 Mar 2023
Cited by: 10 articles | PMID: 36959364
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Clonal haematopoiesis and risk of chronic liver disease.
Wong WJ, Emdin C, Bick AG, Zekavat SM, Niroula A, Pirruccello JP, Dichtel L, Griffin G, Uddin MM, Gibson CJ, Kovalcik V, Lin AE, McConkey ME, Vromman A, Sellar RS, Kim PG, Agrawal M, Weinstock J, Long MT, [...] Natarajan P
Nature, 616(7958):747-754, 12 Apr 2023
Cited by: 47 articles | PMID: 37046084 | PMCID: PMC10405350
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The Genetic Determinants of Aortic Distention.
Pirruccello JP, Rämö JT, Choi SH, Chaffin MD, Kany S, Nekoui M, Chou EL, Jurgens SJ, Friedman SF, Juric D, Stone JR, Batra P, Ng K, Philippakis AA, Lindsay ME, Ellinor PT
J Am Coll Cardiol, 81(14):1320-1335, 01 Apr 2023
Cited by: 6 articles | PMID: 37019578 | PMCID: PMC11246604
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Single-nucleus RNA sequencing in ischemic cardiomyopathy reveals common transcriptional profile underlying end-stage heart failure.
Simonson B, Chaffin M, Hill MC, Atwa O, Guedira Y, Bhasin H, Hall AW, Hayat S, Baumgart S, Bedi KC, Margulies KB, Klattenhoff CA, Ellinor PT
Cell Rep, 42(2):112086, 14 Feb 2023
Cited by: 19 articles | PMID: 36790929 | PMCID: PMC10423750
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Plasma extracellular vesicle transcriptome as a dynamic liquid biopsy in acute heart failure
Gokulnath P, Spanos M, Lehmann HI, Sheng Q, Rodosthenous R, Chaffin M, Varrias D, Chatterjee E, Hutchins E, Li G, Daaboul G, Rana F, Wang AM, Van Keuren-Jensen K, Ellinor PT, Shah R, Das S
medRxiv, 23 Feb 2023
Cited by: 0 articles | PPR: PPR620602
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Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies.
Li X, Quick C, Zhou H, Gaynor SM, Liu Y, Chen H, Selvaraj MS, Sun R, Dey R, Arnett DK, Bielak LF, Bis JC, Blangero J, Boerwinkle E, Bowden DW, Brody JA, Cade BE, Correa A, Cupples LA, [...] Lin X
Nat Genet, 55(1):154-164, 23 Dec 2022
Cited by: 19 articles | PMID: 36564505 | PMCID: PMC10084891
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Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery Disease.
Khera AV, Wang M, Chaffin M, Emdin CA, Samani NJ, Schunkert H, Watkins H, McPherson R, Erdmann J, Elosua R, Boerwinkle E, Ardissino D, Butterworth AS, Di Angelantonio E, Naheed A, Danesh J, Chowdhury R, Krumholz HM, Sheu WH, [...] Kathiresan S
Circ Genom Precis Med, 15(6):e003598, 10 Oct 2022
Cited by: 7 articles | PMID: 36215124 | PMCID: PMC9771961
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Endothelial ARHGEF26 is an angiogenic factor promoting VEGF signalling.
Zhu QM, MacDonald BT, Mizoguchi T, Chaffin M, Leed A, Arduini A, Malolepsza E, Lage K, Kaushik VK, Kathiresan S, Ellinor PT
Cardiovasc Res, 118(13):2833-2846, 01 Oct 2022
Cited by: 3 articles | PMID: 34849650 | PMCID: PMC9586566
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A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
Li Z, Li X, Zhou H, Gaynor SM, Selvaraj MS, Arapoglou T, Quick C, Liu Y, Chen H, Sun R, Dey R, Arnett DK, Auer PL, Bielak LF, Bis JC, Blackwell TW, Blangero J, Boerwinkle E, Bowden DW, [...] Lin X
Nat Methods, 19(12):1599-1611, 27 Oct 2022
Cited by: 41 articles | PMID: 36303018 | PMCID: PMC10008172
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Aortic Cellular Diversity and Quantitative Genome-Wide Association Study Trait Prioritization Through Single-Nuclear RNA Sequencing of the Aneurysmal Human Aorta.
Chou EL, Chaffin M, Simonson B, Pirruccello JP, Akkad AD, Nekoui M, Lino Cardenas CL, Bedi KC, Nash C, Juric D, Stone JR, Isselbacher EM, Margulies KB, Klattenhoff C, Ellinor PT, Lindsay ME
Arterioscler Thromb Vasc Biol, 42(11):1355-1374, 29 Sep 2022
Cited by: 17 articles | PMID: 36172868 | PMCID: PMC9613617
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Whole genome sequence analysis of blood lipid levels in >66,000 individuals.
Selvaraj MS, Li X, Li Z, Pampana A, Zhang DY, Park J, Aslibekyan S, Bis JC, Brody JA, Cade BE, Chuang LM, Chung RH, Curran JE, de las Fuentes L, de Vries PS, Duggirala R, Freedman BI, Graff M, Guo X, [...] Natarajan P
Nat Commun, 13(1):5995, 11 Oct 2022
Cited by: 24 articles | PMID: 36220816 | PMCID: PMC9553944
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Neurocognitive trajectory and proteomic signature of inherited risk for Alzheimer's disease.
Paranjpe MD, Chaffin M, Zahid S, Ritchie S, Rotter JI, Rich SS, Gerszten R, Guo X, Heckbert S, Tracy R, Danesh J, Lander ES, Inouye M, Kathiresan S, Butterworth AS, Khera AV
PLoS Genet, 18(9):e1010294, 01 Sep 2022
Cited by: 3 articles | PMID: 36048760 | PMCID: PMC9436054
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