Amelia Weber Hall, PhD - Publications

Affiliations: 
2003-2007 Biology University of Rochester, Rochester, NY 
 2010-2017 Microbiology University of Texas at Austin, Austin, Texas, U.S.A. 
 2017- Epigenomics Broad Institute of MIT and Harvard, USA 
Area:
genetics, epigenetics, cancer, cardiovascular disease, bioinformatics
Website:
http://ameliaweberhall.net

23 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 Arduini A, Fleming SJ, Xiao L, Hall AW, Akkad AD, Chaffin M, Bendinelli KJ, Tucker NR, Papangeli I, Mantineo H, Babadi M, Stegmann CM, García-Cardeña G, Lindsay ME, Klattenhoff C, et al. Transcriptional profile of the rat cardiovascular system at single cell resolution. Biorxiv : the Preprint Server For Biology. PMID 38014050 DOI: 10.1101/2023.11.14.567085  0.409
2023 Jameson HS, Hanley A, Hill MC, Xiao L, Ye J, Bapat A, Ronzier E, Hall AW, Hucker WJ, Clauss S, Barazza M, Silber E, Mina J, Tucker NR, Mills RW, et al. Loss of the Atrial Fibrillation-Related Gene, , Results in Atrial Dilation and Arrhythmias. Circulation Research. PMID 37449401 DOI: 10.1161/CIRCRESAHA.123.323029  0.551
2023 Khurshid S, Lazarte J, Pirruccello JP, Weng LC, Choi SH, Hall AW, Wang X, Friedman SF, Nauffal V, Biddinger KJ, Aragam KG, Batra P, Ho JE, Philippakis AA, Ellinor PT, et al. Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass. Nature Communications. 14: 1558. PMID 36944631 DOI: 10.1038/s41467-023-37173-w  0.462
2023 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. Single-nucleus RNA sequencing in ischemic cardiomyopathy reveals common transcriptional profile underlying end-stage heart failure. Cell Reports. 42: 112086. PMID 36790929 DOI: 10.1016/j.celrep.2023.112086  0.451
2022 Halford JL, Morrill VN, Choi SH, Jurgens SJ, Melloni G, Marston NA, Weng LC, Nauffal V, Hall AW, Gunn S, Austin-Tse CA, Pirruccello JP, Khurshid S, Rehm HL, Benjamin EJ, et al. Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes. Nature Communications. 13: 5767. PMID 36180445 DOI: 10.1038/s41467-022-33534-z  0.487
2022 Halford JL, Morrill VN, Choi SH, Jurgens SJ, Melloni G, Marston NA, Weng LC, Nauffal V, Hall AW, Gunn S, Austin-Tse CA, Pirruccello JP, Khurshid S, Rehm HL, Benjamin EJ, et al. Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes. Nature Communications. 13: 5106. PMID 36042188 DOI: 10.1038/s41467-022-32009-5  0.494
2022 Nauffal V, Morrill VN, Jurgens SJ, Choi SH, Hall AW, Weng LC, Halford JL, Austin-Tse C, Haggerty CM, Harris SL, Wong EK, Alonso A, Arking DE, Benjamin EJ, Boerwinkle E, et al. Monogenic and Polygenic Contributions to QTc Prolongation in the Population. Circulation. PMID 35389749 DOI: 10.1161/CIRCULATIONAHA.121.057261  0.55
2022 Jurgens SJ, Choi SH, Morrill VN, Chaffin M, Pirruccello JP, Halford JL, Weng LC, Nauffal V, Roselli C, Hall AW, Oetjens MT, Lagerman B, vanMaanen DP, Aragam KG, Lunetta KL, et al. Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank. Nature Genetics. PMID 35177841 DOI: 10.1038/s41588-021-01011-w  0.547
2022 O' Brien S, Holmes AP, Johnson DM, Kabir SN, O' Shea C, O' Reilly M, Avezzu A, Reyat JS, Hall AW, Apicella C, Ellinor PT, Niederer S, Tucker NR, Fabritz L, Kirchhof P, et al. Increased atrial effectiveness of flecainide conferred by altered biophysical properties of sodium channels. Journal of Molecular and Cellular Cardiology. 166: 23-35. PMID 35114252 DOI: 10.1016/j.yjmcc.2022.01.009  0.43
2021 Pirruccello JP, Chaffin MD, Chou EL, Fleming SJ, Lin H, Nekoui M, Khurshid S, Friedman SF, Bick AG, Arduini A, Weng LC, Choi SH, Akkad AD, Batra P, Tucker NR, ... Hall AW, et al. Deep learning enables genetic analysis of the human thoracic aorta. Nature Genetics. PMID 34837083 DOI: 10.1038/s41588-021-00962-4  0.456
2021 Choi SH, Jurgens SJ, Haggerty CM, Hall AW, Halford JL, Morrill VN, Weng LC, Lagerman B, Mirshahi T, Pettinger M, Guo X, Lin HJ, Alonso A, Soliman EZ, Kornej J, et al. Rare Coding Variants Associated with Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-ancestry Analysis. Circulation. Genomic and Precision Medicine. PMID 34319147 DOI: 10.1161/CIRCGEN.120.003300  0.593
2020 Hall AW, Chaffin M, Roselli C, Lin H, Lubitz SA, Bianchi V, Geeven G, Bedi K, Margulies KB, de Laat W, Tucker NR, Ellinor PT. Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation. Circulation. Genomic and Precision Medicine. PMID 33155827 DOI: 10.1161/CIRCGEN.120.003085  0.601
2020 Weng LC, Hall AW, Choi SH, Jurgens SJ, Haessler J, Bihlmeyer NA, Grarup N, Lin H, Teumer A, Li-Gao R, Yao J, Guo X, Brody JA, Müller-Nurasyid M, Schramm K, et al. Genetic Determinants of Electrocardiographic P-wave Duration and Relation to Atrial Fibrillation. Circulation. Genomic and Precision Medicine. PMID 32822252 DOI: 10.1161/CIRCGEN.119.002874  0.566
2020 van Ouwerkerk AF, Hall AW, Kadow ZA, Lazarevic S, Reyat JS, Tucker NR, Nadadur RD, Bosada FM, Bianchi V, Ellinor PT, Fabritz L, Martin JF, de Laat W, Kirchhof P, Moskowitz IP, et al. Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation. Circulation Research. 127: 34-50. PMID 32717170 DOI: 10.1161/CIRCRESAHA.120.316574  0.598
2020 Ntalla I, Weng LC, Cartwright JH, Hall AW, Sveinbjornsson G, Tucker NR, Choi SH, Chaffin MD, Roselli C, Barnes MR, Mifsud B, Warren HR, Hayward C, Marten J, Cranley JJ, et al. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Nature Communications. 11: 2542. PMID 32439900 DOI: 10.1038/S41467-020-15706-X  0.567
2020 Tucker NR, Chaffin M, Fleming SJ, Hall AW, Parsons VA, Bedi KC, Akkad AD, Herndon CN, Arduini A, Papangeli I, Roselli C, Aguet F, Choi SH, Ardlie KG, Babadi M, et al. Transcriptional and Cellular Diversity of the Human Heart. Circulation. PMID 32403949 DOI: 10.1161/Circulationaha.119.045401  0.536
2019 Choi SH, Jurgens SJ, Weng LC, Pirruccello JP, Roselli C, Chaffin M, Lee C, Hall AW, Khera AV, Lunetta K, Lubitz SA, Ellinor PT. Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results from a National Biobank. Circulation Research. PMID 31691645 DOI: 10.1161/CIRCRESAHA.119.315686  0.566
2019 Zhang M, Hill MC, Kadow ZA, Suh JH, Tucker NR, Hall AW, Tran TT, Swinton PS, Leach JP, Margulies KB, Ellinor PT, Li N, Martin JF. Long-range enhancer-promoter interactions prevent predisposition to atrial fibrillation. Proceedings of the National Academy of Sciences of the United States of America. PMID 31636200 DOI: 10.1073/Pnas.1907418116  0.542
2018 Hall AW, Battenhouse AM, Shivram H, Morris AR, Cowperthwaite MC, Shpak M, Iyer VR. Bivalent chromatin domains in glioblastoma reveal a subtype-specific signature of glioma stem cells. Cancer Research. PMID 29549165 DOI: 10.1158/0008-5472.Can-17-1724  0.645
2015 Mohanty S, Hall AW, Mohanty P, Prakash S, Trivedi C, Di Biase L, Santangeli P, Bai R, Burkhardt JD, Gallinghouse GJ, Horton R, Sanchez JE, Hranitzky PM, Al-Ahmad A, Iyer VR, et al. Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF). Journal of Interventional Cardiac Electrophysiology : An International Journal of Arrhythmias and Pacing. PMID 26497660 DOI: 10.1007/S10840-015-0069-2  0.606
2014 Shpak M, Hall AW, Goldberg MM, Derryberry DZ, Ni Y, Iyer VR, Cowperthwaite MC. An eQTL analysis of the human glioblastoma multiforme genome. Genomics. 103: 252-63. PMID 24607568 DOI: 10.1016/J.Ygeno.2014.02.005  0.645
2012 Ni Y, Hall AW, Battenhouse A, Iyer VR. Simultaneous SNP identification and assessment of allele-specific bias from ChIP-seq data. Bmc Genetics. 13: 46. PMID 22950704 DOI: 10.1186/1471-2156-13-46  0.597
2008 Seluanov A, Hine C, Bozzella M, Hall A, Sasahara TH, Ribeiro AA, Catania KC, Presgraves DC, Gorbunova V. Distinct tumor suppressor mechanisms evolve in rodent species that differ in size and lifespan. Aging Cell. 7: 813-23. PMID 18778411 DOI: 10.1111/J.1474-9726.2008.00431.X  0.462
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