Nikola Teslovich - Related publications

Affiliations: 
Genetics Brigham & Women's Hospital, Harvard Medical School, Boston, MA, United States 
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50 most relevant papers in past 60 days:
Year Citation  Score
2021 Chen JK, Kashgari G, Andersen B. Capturing New Disease Genes in Psoriasis and Other Skin Diseases. The Journal of Investigative Dermatology. 141: 1881-1884. PMID 34303468 DOI: 10.1016/j.jid.2021.04.004   
2021 Claussnitzer M, Susztak K. Gaining insight into metabolic diseases from human genetic discoveries. Trends in Genetics : Tig. PMID 34315631 DOI: 10.1016/j.tig.2021.07.005   
2021 Joslin AC, Sobreira DR, Hansen GT, Sakabe NJ, Aneas I, Montefiori LE, Farris KM, Gu J, Lehman DM, Ober C, He X, Nóbrega MA. A functional genomics pipeline identifies pleiotropy and cross-tissue effects within obesity-associated GWAS loci. Nature Communications. 12: 5253. PMID 34489471 DOI: 10.1038/s41467-021-25614-3   
2021 Sheng X, Guan Y, Ma Z, Wu J, Liu H, Qiu C, Vitale S, Miao Z, Seasock MJ, Palmer M, Shin MK, Duffin KL, Pullen SS, Edwards TL, Hellwege JN, et al. Mapping the genetic architecture of human traits to cell types in the kidney identifies mechanisms of disease and potential treatments. Nature Genetics. PMID 34385711 DOI: 10.1038/s41588-021-00909-9   
2021 Zhang Y, Wang Y, Zhou W, Zheng S, Ye R. Detection of candidate gene networks involved in resistance to Sclerotinia sclerotiorum in soybean. Journal of Applied Genetics. PMID 34510383 DOI: 10.1007/s13353-021-00654-z   
2021 Wang Q, Dhindsa RS, Carss K, Harper AR, Nag A, Tachmazidou I, Vitsios D, Deevi SVV, Mackay A, Muthas D, Hühn M, Monkley S, Olsson H, , Wasilewski S, et al. Rare variant contribution to human disease in 281,104 UK Biobank exomes. Nature. PMID 34375979 DOI: 10.1038/s41586-021-03855-y   
2021 Mulvey B, Dougherty JD. Transcriptional-regulatory convergence across functional MDD risk variants identified by massively parallel reporter assays. Translational Psychiatry. 11: 403. PMID 34294677 DOI: 10.1038/s41398-021-01493-6   
2021 Lee H, Metz A, McDiarmid A, Palmos A, Lee SH, Curtis CJ, Patel H, Newhouse SJ, Thuret S. The effects of genotype on inflammatory response in hippocampal progenitor cells: A computational approach. Brain, Behavior, & Immunity - Health. 15: 100286. PMID 34345870 DOI: 10.1016/j.bbih.2021.100286   
2021 Khetan S, Kales S, Kursawe R, Jillette A, Ulirsch JC, Reilly SK, Ucar D, Tewhey R, Stitzel ML. Functional characterization of T2D-associated SNP effects on baseline and ER stress-responsive β cell transcriptional activation. Nature Communications. 12: 5242. PMID 34475398 DOI: 10.1038/s41467-021-25514-6   
2021 Arendt M, Ambrosen A, Fall T, Kierczak M, Tengvall K, Meadows JRS, Karlsson Å, Lagerstedt AS, Bergström T, Andersson G, Lindblad-Toh K, Hagman R. The ABCC4 gene is associated with pyometra in golden retriever dogs. Scientific Reports. 11: 16647. PMID 34404837 DOI: 10.1038/s41598-021-95936-1   
2021 Wong AK, Sealfon RSG, Theesfeld CL, Troyanskaya OG. Decoding disease: from genomes to networks to phenotypes. Nature Reviews. Genetics. PMID 34341555 DOI: 10.1038/s41576-021-00389-x   
2021 Fisher V, Sebastiani P, Cupples LA, Liu CT. ANNORE: Genetic fine mapping with functional annotation. Human Molecular Genetics. PMID 34302344 DOI: 10.1093/hmg/ddab210   
2021 Fisher V, Sebastiani P, Cupples LA, Liu CT. ANNORE: Genetic fine mapping with functional annotation. Human Molecular Genetics. PMID 34302344 DOI: 10.1093/hmg/ddab210   
2021 Jan A, Saeed M, Afridi MH, Khuda F, Shabbir M, Khan H, Ali S, Hassan M, Samiullah, Akbar R, Zakiullah. Association of HLA-B Gene Polymorphisms with Type 2 Diabetes in Pashtun Ethnic Population of Khyber Pakhtunkhwa, Pakistan. Journal of Diabetes Research. 2021: 6669731. PMID 34258292 DOI: 10.1155/2021/6669731   
2021 Sofer T, Lee J, Kurniansyah N, Jain D, Laurie CA, Gogarten SM, Conomos MP, Heavner B, Hu Y, Kooperberg C, Haessler J, Vasan RS, Cupples LA, Coombes BJ, Seyerle A, ... , et al. BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion. Hgg Advances. 2. PMID 34337551 DOI: 10.1016/j.xhgg.2021.100040   
2021 Mo A, Nagpal S, Gettler K, Haritunians T, Giri M, Haberman Y, Karns R, Prince J, Arafat D, Hsu NY, Chuang LS, Argmann C, Kasarskis A, Suarez-Farinas M, Gotman N, et al. Stratification of risk of progression to colectomy in ulcerative colitis via measured and predicted gene expression. American Journal of Human Genetics. PMID 34450030 DOI: 10.1016/j.ajhg.2021.07.013   
2021 Hu Y, Qiu S, Cheng L. Integration of Multiple-Omics Data to Analyze the Population-Specific Differences for Coronary Artery Disease. Computational and Mathematical Methods in Medicine. 2021: 7036592. PMID 34447459 DOI: 10.1155/2021/7036592   
2021 Cui Y, Peng F, Wang D, Li Y, Li JS, Li L, Li W. 3'aQTL-atlas: an atlas of 3'UTR alternative polyadenylation quantitative trait loci across human normal tissues. Nucleic Acids Research. PMID 34432052 DOI: 10.1093/nar/gkab740   
2021 Lalami I, Abo C, Borghese B, Chapron C, Vaiman D. Genomics of Endometriosis: From Genome Wide Association Studies to Exome Sequencing. International Journal of Molecular Sciences. 22. PMID 34298916 DOI: 10.3390/ijms22147297   
2021 Chen J, Ali MW, Yan L, Dighe SG, Dai JY, Vaughan TL, Casey G, Buas MF. Prioritization and functional analysis of GWAS risk loci for Barrett's esophagus and esophageal adenocarcinoma. Human Molecular Genetics. PMID 34505128 DOI: 10.1093/hmg/ddab259   
2021 Sin S, Choi HM, Lim J, Kim J, Bak SH, Choi SS, Park J, Lee JH, Oh YM, Lee MK, Hobbs BD, Cho MH, Silverman EK, Kim WJ. A genome-wide association study of quantitative computed tomographic emphysema in Korean populations. Scientific Reports. 11: 16692. PMID 34404834 DOI: 10.1038/s41598-021-95887-7   
2021 Yadav T, Magotra A, Bangar YC, Kumar R, Yadav AS, Garg AR, Bahurupi P, Kumar P. Effect of I genotyped intronic SNP of leptin gene on production and reproduction traits in Indian dairy cattle. Animal Biotechnology. 1-7. PMID 34370619 DOI: 10.1080/10495398.2021.1955701   
2021 Nair V, Sankaranarayanan R, Vasavada AR. Deciphering the association of intronic single nucleotide polymorphisms of crystallin gene family with congenital cataract. Indian Journal of Ophthalmology. 69: 2064-2070. PMID 34304179 DOI: 10.4103/ijo.IJO_3062_20   
2021 Nair V, Sankaranarayanan R, Vasavada AR. Deciphering the association of intronic single nucleotide polymorphisms of crystallin gene family with congenital cataract. Indian Journal of Ophthalmology. 69: 2064-2070. PMID 34304179 DOI: 10.4103/ijo.IJO_3062_20   
2021 Chamarthi SK, Kaler AS, Abdel-Haleem H, Fritschi FB, Gillman JD, Ray JD, Smith JR, Dhanapal AP, King CA, Purcell LC. Identification and Confirmation of Loci Associated With Canopy Wilting in Soybean Using Genome-Wide Association Mapping. Frontiers in Plant Science. 12: 698116. PMID 34335664 DOI: 10.3389/fpls.2021.698116   
2021 Guan Y, Liang X, Ma Z, Hu H, Liu H, Miao Z, Linkermann A, Hellwege JN, Voight BF, Susztak K. A single genetic locus controls both expression of DPEP1/CHMP1A and kidney disease development via ferroptosis. Nature Communications. 12: 5078. PMID 34426578 DOI: 10.1038/s41467-021-25377-x   
2021 Sun Y, Zhu J, Zhou D, Canchi S, Wu C, Cox NJ, Rissman RA, Gamazon ER, Wu L. A transcriptome-wide association study of Alzheimer's disease using prediction models of relevant tissues identifies novel candidate susceptibility genes. Genome Medicine. 13: 141. PMID 34470669 DOI: 10.1186/s13073-021-00959-y   
2021 Abdalla IM, Lu X, Nazar M, Arbab AAI, Xu T, Yousif MH, Mao Y, Yang Z. Genome-Wide Association Study Identifies Candidate Genes Associated with Feet and Leg Conformation Traits in Chinese Holstein Cattle. Animals : An Open Access Journal From Mdpi. 11. PMID 34438715 DOI: 10.3390/ani11082259   
2021 Lee YL, Takeda H, Costa Monteiro Moreira G, Karim L, Mullaart E, Coppieters W, , Appeltant R, Veerkamp RF, Groenen MAM, Georges M, Bosse M, Druet T, Bouwman AC, Charlier C. A 12 kb multi-allelic copy number variation encompassing a GC gene enhancer is associated with mastitis resistance in dairy cattle. Plos Genetics. 17: e1009331. PMID 34288907 DOI: 10.1371/journal.pgen.1009331   
2021 Lee YL, Takeda H, Costa Monteiro Moreira G, Karim L, Mullaart E, Coppieters W, , Appeltant R, Veerkamp RF, Groenen MAM, Georges M, Bosse M, Druet T, Bouwman AC, Charlier C. A 12 kb multi-allelic copy number variation encompassing a GC gene enhancer is associated with mastitis resistance in dairy cattle. Plos Genetics. 17: e1009331. PMID 34288907 DOI: 10.1371/journal.pgen.1009331   
2021 Brandt M, Kim-Hellmuth S, Ziosi M, Gokden A, Wolman A, Lam N, Recinos Y, Daniloski Z, Morris JA, Hornung V, Schumacher J, Lappalainen T. An autoimmune disease risk variant: A trans master regulatory effect mediated by IRF1 under immune stimulation? Plos Genetics. 17: e1009684. PMID 34314424 DOI: 10.1371/journal.pgen.1009684   
2021 Cha J, Choo H, Srikanth K, Lee SH, Son JW, Park MR, Kim N, Jang GW, Park JE. Genome-Wide Association Study Identifies 12 Loci Associated with Body Weight at Age 8 Weeks in Korean Native Chickens. Genes. 12. PMID 34440344 DOI: 10.3390/genes12081170   
2021 Wang S, Said MA, Groot HE, van der Most PJ, Thio CHL, van de Vegte YJ, Verweij N, Snieder H, van der Harst P. Search for a Functional Genetic Variant Mimicking the Effect of SGLT2 Inhibitor Treatment. Genes. 12. PMID 34440348 DOI: 10.3390/genes12081174   
2021 Abdelmajed SS, El-Dessouky MA, SalahElDin DS, Hassan NA, Zaki ME, Ismail S. Assessing the association of rs7574865 STAT4 gene variant and type 1 diabetes mellitus among Egyptian patients. Journal, Genetic Engineering & Biotechnology. 19: 112. PMID 34342790 DOI: 10.1186/s43141-021-00214-2   
2021 Asiri A, Alwadaani D, Umair M, Alhamoudi KM, Almuhanna MH, Nasir A, Alrfaei BM, Al Tuwaijri A, Barhoumi T, Alyafee Y, Almuzzaini B, Aldrees M, Ballow M, Alayyar L, Al Abdulrahman A, et al. Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo Gene Defect: Expanding the Molecular and Phenotypic Spectrum. Genes. 12. PMID 33672558 DOI: 10.3390/genes12020294   
2021 Lains I, Zhu S, Han X, Chung W, Yuan Q, Kelly RS, Gil JQ, Katz R, Nigalye A, Kim IK, Miller JB, Carreira IM, Silva R, Vavvas DG, Miller JW, et al. Genomic-Metabolomic Associations Support the Role of and Glycerophospholipids in Age-Related Macular Degeneration. Ophthalmology Science. 1. PMID 34382031 DOI: 10.1016/j.xops.2021.100017   
2021 Canive M, González-Recio O, Fernández A, Vázquez P, Badia-Bringué G, Lavín JL, Garrido JM, Juste RA, Alonso-Hearn M. Identification of loci associated with susceptibility to Mycobacterium avium subsp. paratuberculosis infection in Holstein cattle using combinations of diagnostic tests and imputed whole-genome sequence data. Plos One. 16: e0256091. PMID 34449805 DOI: 10.1371/journal.pone.0256091   
2021 Melak S, Wang Q, Tian Y, Wei W, Zhang L, Elbeltagy A, Chen J. Identification and Validation of Marketing Weight-Related SNP Markers Using SLAF Sequencing in Male Yangzhou Geese. Genes. 12. PMID 34440377 DOI: 10.3390/genes12081203   
2021 Sun H, Lan X, Ma L, Zhou J. Revealing modifier variations characterizations for elucidating the genetic basis of human phenotypic variations. Human Genetics. PMID 34498116 DOI: 10.1007/s00439-021-02362-4   
2021 Dong C, Simonett SP, Shin S, Stapleton DS, Schueler KL, Churchill GA, Lu L, Liu X, Jin F, Li Y, Attie AD, Keller MP, Keleş S. INFIMA leverages multi-omics model organism data to identify effector genes of human GWAS variants. Genome Biology. 22: 241. PMID 34425882 DOI: 10.1186/s13059-021-02450-8   
2021 Ding J, Frantzeskos A, Orozco G. Functional interrogation of autoimmune disease genetics using CRISPR/Cas9 technologies and massively parallel reporter assays. Seminars in Immunopathology. PMID 34508276 DOI: 10.1007/s00281-021-00887-4   
2021 van Eyk CL, Webber DL, Minoche AE, Pérez-Jurado LA, Corbett MA, Gardner AE, Berry JG, Harper K, MacLennan AH, Gecz J. Yield of clinically reportable genetic variants in unselected cerebral palsy by whole genome sequencing. Npj Genomic Medicine. 6: 74. PMID 34531397 DOI: 10.1038/s41525-021-00238-0   
2021 Yaoxing H, Danchun Y, Xiaojuan S, Shuman J, Qingqing Y, Lin J. Identification of Novel Susceptible Genes of Gastric Cancer Based on Integrated Omics Data. Frontiers in Cell and Developmental Biology. 9: 712020. PMID 34354996 DOI: 10.3389/fcell.2021.712020   
2021 Lee KD, Millar CD, Brekke P, Whibley A, Ewen JG, Hingston M, Zhu A, Santure AW. The design and application of a 50K SNP chip for a threatened Aotearoa New Zealand passerine, the hihi. Molecular Ecology Resources. PMID 34323011 DOI: 10.1111/1755-0998.13480   
2021 Lee KD, Millar CD, Brekke P, Whibley A, Ewen JG, Hingston M, Zhu A, Santure AW. The design and application of a 50K SNP chip for a threatened Aotearoa New Zealand passerine, the hihi. Molecular Ecology Resources. PMID 34323011 DOI: 10.1111/1755-0998.13480   
2021 Griesemer D, Xue JR, Reilly SK, Ulirsch JC, Kukreja K, Davis JR, Kanai M, Yang DK, Butts JC, Guney MH, Luban J, Montgomery SB, Finucane HK, Novina CD, Tewhey R, et al. Genome-wide functional screen of 3'UTR variants uncovers causal variants for human disease and evolution. Cell. PMID 34534445 DOI: 10.1016/j.cell.2021.08.025   
2021 Hariharan P, Dupuis J. Mapping gene and gene pathways associated with coronary artery disease: a CARDIoGRAM exome and multi-ancestry UK biobank analysis. Scientific Reports. 11: 16461. PMID 34385509 DOI: 10.1038/s41598-021-95637-9   
2021 Zhu J, Yang Y, Kisiel JB, Mahoney DW, Michaud DS, Guo X, Taylor WR, Shu XO, Shu X, Liu D, Li B, Tao R, Cai Q, Zheng W, Long J, et al. Integrating genome and methylome data to identify candidate DNA methylation biomarkers for pancreatic cancer risk. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 34497089 DOI: 10.1158/1055-9965.EPI-21-0400   
2021 Long SY, Wang L, Jiang HQ, Shi Y, Zhang WY, Xiong JS, Sun PW, Chen YQ, Mei YM, Pan C, Ge G, Wang ZZ, Wu ZW, Yu MW, Wang HS. Single-Nucleotide Polymorphisms Related to Leprosy Risk and Clinical Phenotypes Among Chinese Population. Pharmacogenomics and Personalized Medicine. 14: 813-821. PMID 34285550 DOI: 10.2147/PGPM.S314861   
2021 Seddon JM, Fortes M, Kelly-Smith M, Sommerlad SF, Hayward JJ, Burmeister L, De Risio L, Mellersh C, Freeman J, Strain GM. Deafness in Australian Cattle Dogs associated to QTL on chromosome 20 in genome-wide association study analyses. Animal Genetics. PMID 34318504 DOI: 10.1111/age.13115