Anelia Horvath - Publications

Affiliations: 
Biomedical Sciences The George Washington University, Washington, DC, United States 
Area:
Oncology, Bioinformatics Biology, Molecular Biology

36 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
2021 Liu H, Prashant NM, Spurr LF, Bousounis P, Alomran N, Ibeawuchi H, Sein J, Słowiński P, Tsaneva-Atanasova K, Horvath A. scReQTL: an approach to correlate SNVs to gene expression from individual scRNA-seq datasets. Bmc Genomics. 22: 40. PMID 33419390 DOI: 10.1186/s12864-020-07334-y  0.32
2020 Słowiński P, Li M, Restrepo P, Alomran N, Spurr LF, Miller C, Tsaneva-Atanasova K, Horvath A. GeTallele: A Method for Analysis of DNA and RNA Allele Frequency Distributions. Frontiers in Bioengineering and Biotechnology. 8: 1021. PMID 33042959 DOI: 10.3389/Fbioe.2020.01021  0.32
2020 Zhang M, Jiang N, Chu Y, Postnikova O, Varghese R, Horvath A, Cheema AK, Golestaneh N. Dysregulated metabolic pathways in age-related macular degeneration. Scientific Reports. 10: 2464. PMID 32051464 DOI: 10.1038/S41598-020-59244-4  0.36
2019 Spurr L, Alomran N, Bousounis P, Reece-Stremtan D, Prashant NM, Liu H, Słowiński P, Li M, Zhang Q, Sein J, Asher G, Crandall KA, Tsaneva-Atanasova K, Horvath A. ReQTL: Identifying correlations between expressed SNVs and gene expression using RNA-sequencing data. Bioinformatics (Oxford, England). PMID 31589315 DOI: 10.1093/Bioinformatics/Btz750  0.32
2019 Shetty K, Deng C, Jogunoori WS, Amdur R, Resar LS, Latham P, Mazumder R, Horvath A, Nguyen B, Li S, Wu X, Yu H, Wong LL, White J, Silver S, et al. Abstract 3156: Pathway Specific Functional Biomarkers for the Early Detection of Liver Cancer Cancer Research. 79: 3156-3156. DOI: 10.1158/1538-7445.Sabcs18-3156  0.36
2018 Spurr L, Li M, Alomran N, Zhang Q, Restrepo P, Movassagh M, Trenkov C, Tunnessen N, Apanasovich T, Crandall KA, Edwards N, Horvath A. Systematic pan-cancer analysis of somatic allele frequency. Scientific Reports. 8: 7735. PMID 29769535 DOI: 10.1038/S41598-018-25462-0  0.6
2017 Chen J, Zaidi S, Rao S, Chen JS, Phan L, Farci P, Su X, Shetty K, White J, Zamboni F, Wu X, Rashid A, Pattabiraman N, Mazumder R, Horvath A, et al. Analysis of Genomes and Transcriptomes of Hepatocellular Carcinomas Identifies Mutations and Gene Expression Changes in the Transforming Growth Factor beta Pathway Short title: Prognostic significance of TGF-β signature in liver cancer. Gastroenterology. PMID 28918914 DOI: 10.1053/J.Gastro.2017.09.007  0.36
2017 Restrepo P, Movassagh M, Alomran N, Miller C, Li M, Trenkov C, Manchev Y, Bahl S, Warnken S, Spurr L, Apanasovich T, Crandall K, Edwards N, Horvath A. Overexpressed somatic alleles are enriched in functional elements in Breast Cancer. Scientific Reports. 7: 8287. PMID 28811643 DOI: 10.1038/S41598-017-08416-W  0.6
2017 Movassagh M, Mudvari P, Horvath A. Co-Occurrence of COMT and BRCA1/2 Variants in a Population. The New England Journal of Medicine. 376: 2090-2091. PMID 28538113 DOI: 10.1056/Nejmc1701592  0.6
2016 Movassagh M, Alomran N, Mudvari P, Dede M, Dede C, Kowsari K, Restrepo P, Cauley E, Bahl S, Li M, Waterhouse W, Tsaneva-Atanasova K, Edwards N, Horvath A. RNA2DNAlign: nucleotide resolution allele asymmetries through quantitative assessment of RNA and DNA paired sequencing data. Nucleic Acids Research. PMID 27576531 DOI: 10.1093/Nar/Gkw757  0.6
2015 London E, Wassif CA, Horvath A, Tatsi C, Angelousi A, Karageorgiadis AS, Porter FD, Stratakis CA. Cholesterol biosynthesis and trafficking in cortisol-producing lesions of the adrenal cortex. The Journal of Clinical Endocrinology and Metabolism. jc20152212. PMID 26204136 DOI: 10.1210/Jc.2015-2212  0.36
2015 Faucz FR, Horvath AD, Azevedo MF, Levy I, Bak B, Wang Y, Xekouki P, Szarek E, Gourgari E, Manning AD, de Alexandre RB, Saloustros E, Trivellin G, Lodish M, Hofman P, et al. Is IGSF1 involved in human pituitary tumor formation? Endocrine-Related Cancer. 22: 47-54. PMID 25527509 DOI: 10.1530/ERC-14-0465  0.36
2015 Mudvari P, Movassagh M, Kowsari K, Seyfi A, Kokkinaki M, Edwards NJ, Golestaneh N, Horvath A. SNPlice: variants that modulate Intron retention from RNA-sequencing data. Bioinformatics (Oxford, England). 31: 1191-8. PMID 25481010 DOI: 10.1093/Bioinformatics/Btu804  0.36
2014 Trivellin G, Daly AF, Faucz FR, Yuan B, Rostomyan L, Larco DO, Schernthaner-Reiter MH, Szarek E, Leal LF, Caberg JH, Castermans E, Villa C, Dimopoulos A, Chittiboina P, Xekouki P, ... ... Horvath A, et al. Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation. The New England Journal of Medicine. 371: 2363-74. PMID 25470569 DOI: 10.1056/Nejmoa1408028  0.36
2014 Azevedo MF, Faucz FR, Bimpaki E, Horvath A, Levy I, de Alexandre RB, Ahmad F, Manganiello V, Stratakis CA. Clinical and molecular genetics of the phosphodiesterases (PDEs). Endocrine Reviews. 35: 195-233. PMID 24311737 DOI: 10.1210/Er.2013-1053  0.36
2014 Salpea P, Horvath A, London E, Faucz FR, Vetro A, Levy I, Gourgari E, Dauber A, Holm IA, Morrison PJ, Keil MF, Lyssikatos C, Smith ED, Sanidad MA, Kelly JC, et al. Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testing. The Journal of Clinical Endocrinology and Metabolism. 99: E183-8. PMID 24170103 DOI: 10.1210/Jc.2013-3159  0.36
2014 Guillaud Bataille M, Rhayem Y, Sousa SB, Libé R, Dambrun M, Chevalier C, Nigou M, Auzan C, North MO, Sa J, Gomes L, Salpea P, Horvath A, Stratakis CA, Hamzaoui N, et al. Systematic screening for PRKAR1A gene rearrangement in Carney complex: identification and functional characterization of a new in-frame deletion. European Journal of Endocrinology / European Federation of Endocrine Societies. 170: 151-60. PMID 24144965 DOI: 10.1530/Eje-13-0740  0.36
2013 Mudvari P, Kowsari K, Cole C, Mazumder R, Horvath A. Extraction of Molecular Features through Exome to Transcriptome Alignment. Journal of Metabolomics and Systems Biology. 1. PMID 24791251 DOI: 10.13188/2329-1583.1000002  0.6
2013 Mudvari P, Ohshiro K, Nair V, Horvath A, Kumar R. Genomic insights into triple-negative and HER2-positive breast cancers using isogenic model systems. Plos One. 8: e74993. PMID 24086418 DOI: 10.1371/Journal.Pone.0074993  0.6
2013 Horvath A, Pakala SB, Mudvari P, Reddy SD, Ohshiro K, Casimiro S, Pires R, Fuqua SA, Toi M, Costa L, Nair SS, Sukumar S, Kumar R. Novel insights into breast cancer genetic variance through RNA sequencing. Scientific Reports. 3: 2256. PMID 23884293 DOI: 10.1038/Srep02256  0.6
2013 Eswaran J, Horvath A, Godbole S, Reddy SD, Mudvari P, Ohshiro K, Cyanam D, Nair S, Fuqua SA, Polyak K, Florea LD, Kumar R. RNA sequencing of cancer reveals novel splicing alterations. Scientific Reports. 3: 1689. PMID 23604310 DOI: 10.1038/Srep01689  0.36
2013 Kumar R, Horvath A, Mazumder R, Toi M, Sato F, Pillai MR, Costa L, Carmo-Fonseca M, Knapp S, Dutt A, Gupta S, Badwe R. The Global Cancer Genomics Consortium's Second Annual Symposium: Genomics Medicine in Cancer Research Genes and Cancer. 4: 196-200. DOI: 10.1177/1947601913484582  0.36
2012 Xekouki P, Hatch MM, Lin L, Rodrigo de A, Azevedo M, de la Luz Sierra M, Levy I, Saloustros E, Moraitis A, Horvath A, Kebebew E, Hoffman DA, Stratakis CA. KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome. Endocrine-Related Cancer. 19: 255-60. PMID 22323562 DOI: 10.1530/Erc-12-0022  0.36
2012 Patronas Y, Horvath A, Greene E, Tsang K, Bimpaki E, Haran M, Nesterova M, Stratakis CA. In vitro studies of novel PRKAR1A mutants that extend the predicted RIα protein sequence into the 3'-untranslated open reading frame: proteasomal degradation leads to RIα haploinsufficiency and Carney complex. The Journal of Clinical Endocrinology and Metabolism. 97: E496-502. PMID 22205709 DOI: 10.1210/Jc.2011-2220  0.36
2011 Almeida MQ, Harran M, Bimpaki EI, Hsiao HP, Horvath A, Cheadle C, Watkins T, Nesterova M, Stratakis CA. Integrated genomic analysis of nodular tissue in macronodular adrenocortical hyperplasia: progression of tumorigenesis in a disorder associated with multiple benign lesions. The Journal of Clinical Endocrinology and Metabolism. 96: E728-38. PMID 21252250 DOI: 10.1210/Jc.2010-2420  0.36
2010 Stratakis CA, Tichomirowa MA, Boikos S, Azevedo MF, Lodish M, Martari M, Verma S, Daly AF, Raygada M, Keil MF, Papademetriou J, Drori-Herishanu L, Horvath A, Tsang KM, Nesterova M, et al. The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes Clinical Genetics. 78: 457-463. PMID 20507346 DOI: 10.1111/J.1399-0004.2010.01406.X  0.36
2010 Louiset E, Gobet F, Libé R, Horvath A, Renouf S, Cariou J, Rothenbuhler A, Bertherat J, Clauser E, Grise P, Stratakis CA, Kuhn JM, Lefebvre H. ACTH-independent Cushing's syndrome with bilateral micronodular adrenal hyperplasia and ectopic adrenocortical adenoma. The Journal of Clinical Endocrinology and Metabolism. 95: 18-24. PMID 19915020 DOI: 10.1210/Jc.2009-0881  0.36
2008 Greene EL, Horvath AD, Nesterova M, Giatzakis C, Bossis I, Stratakis CA. In vitro functional studies of naturally occurring pathogenic PRKAR1A mutations that are not subject to nonsense mRNA decay. Human Mutation. 29: 633-9. PMID 18241045 DOI: 10.1002/humu.20688  0.36
2006 Horvath A, Boikos S, Giatzakis C, Robinson-White A, Groussin L, Griffin KJ, Stein E, Levine E, Delimpasi G, Hsiao HP, Keil M, Heyerdahl S, Matyakhina L, Libè R, Fratticci A, et al. A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia. Nature Genetics. 38: 794-800. PMID 16767104 DOI: 10.1038/Ng1809  0.36
2004 Andonova IE, Sarueva RB, Horvath AD, Simeonov VA, Dimitrov PS, Petropoulos EA, Ganev VS. Balkan endemic nephropathy and genetic variants of glutathione S-transferases. Journal of Nephrology. 17: 390-8. PMID 15365959  0.36
2004 Mihaylov VA, Horvath AD, Savov AS, Kurshelova EF, Paskaleva ID, Goudev AR, Stoilov IR, Ganev VS. Screening for point mutations in the LDL receptor gene in Bulgarian patients with severe hypercholesterolemia Journal of Human Genetics. 49: 173-176. PMID 15015036 DOI: 10.1007/s10038-004-0127-6  0.36
2003 Horvath A, Chorbov V, Zaharova B, Ganev V. Five polymorphisms of the apolipoprotein B gene in healthy bulgarians Human Biology. 75: 69-80. PMID 12713147 DOI: 10.1353/Hub.2003.0022  0.36
2003 Upham BL, Koski TR, Rummel AM, Wilson MR, Horvath A, Trosko JE. Differential roles of 2, 6, and 8 carbon ceramides on the modulation of gap junctional communication and apoptosis during carcinogenesis. Cancer Letters. 191: 27-34. PMID 12609706 DOI: 10.1016/S0304-3835(02)00620-1  0.36
2001 Horvath A, Upham BL, Ganev V, Trosko JE. Determination of the epigenetic effects of ochratoxin in a human kidney and a rat liver epithelial cell line Toxicon. 40: 273-282. PMID 11711124 DOI: 10.1016/S0041-0101(01)00219-7  0.36
2001 Horvath A, Savov A, Kirov S, Karshelova E, Paskaleva I, Goudev A, Ganev V. High frequency of the ApoB-100 R3500Q mutation in Bulgarian hypercholesterolaemic subjects [4] Journal of Medical Genetics. 38: 536-540. PMID 11494965 DOI: 10.1136/Jmg.38.8.536  0.36
2001 Horvath A, Ganev V. The mutation APOB-100 R3500Q in Eastern Europe [2] Atherosclerosis. 156: 241-242. PMID 11417523 DOI: 10.1016/S0021-9150(01)00482-8  0.36
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