11/17 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 Yilmaz F, Karageorgiou C, Kim K, Pajic P, Beck CR, Torregrossa AM, Lee C, Gokcumen O. Ancient gene duplications primed the amylase locus for adaptive evolution upon the onset of agriculture. Biorxiv : the Preprint Server For Biology. PMID 38077078 DOI: 10.1101/2023.11.27.568916  0.493
2023 Hallast P, Ebert P, Loftus M, Yilmaz F, Audano PA, Logsdon GA, Bonder MJ, Zhou W, Höps W, Kim K, Li C, Hoyt SJ, Dishuck PC, Porubsky D, Tsetsos F, et al. Assembly of 43 human Y chromosomes reveals extensive complexity and variation. Nature. PMID 37612510 DOI: 10.1038/s41586-023-06425-6  0.567
2023 Yilmaz F, Gurusamy U, Mosley TJ, Hallast P, Kim K, Mostovoy Y, Purcell RH, Shaikh TH, Zwick ME, Kwok PY, Lee C, Mulle JG. High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing. Genome Medicine. 15: 35. PMID 37165454 DOI: 10.1186/s13073-023-01184-5  0.553
2022 Porubsky D, Höps W, Ashraf H, Hsieh P, Rodriguez-Martin B, Yilmaz F, Ebler J, Hallast P, Maria Maggiolini FA, Harvey WT, Henning B, Audano PA, Gordon DS, Ebert P, Hasenfeld P, et al. Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders. Cell. PMID 35525246 DOI: 10.1016/j.cell.2022.04.017  0.564
2022 Danis D, Jacobsen JOB, Balachandran P, Zhu Q, Yilmaz F, Reese J, Haimel M, Lyon GJ, Helbig I, Mungall CJ, Beck CR, Lee C, Smedley D, Robinson PN. SvAnna: efficient and accurate pathogenicity prediction of coding and regulatory structural variants in long-read genome sequencing. Genome Medicine. 14: 44. PMID 35484572 DOI: 10.1186/s13073-022-01046-6  0.513
2022 Null M, Yilmaz F, Astling D, Yu HC, Cole JB, Hallgrímsson B, Santorico SA, Spritz RA, Shaikh TH, Hendricks AE. Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans. Hgg Advances. 3: 100082. PMID 35047866 DOI: 10.1016/j.xhgg.2021.100082  0.39
2021 Yilmaz F, Null M, Astling D, Yu HC, Cole J, Santorico SA, Hallgrimsson B, Manyama M, Spritz RA, Hendricks AE, Shaikh TH. Genome-wide copy number variations in a large cohort of bantu African children. Bmc Medical Genomics. 14: 129. PMID 34001112 DOI: 10.1186/s12920-021-00978-z  0.458
2021 Mostovoy Y, Yilmaz F, Chow SK, Chu C, Lin C, Geiger EA, Meeks NJL, Chatfield KC, Coughlin CR, Surti U, Kwok PY, Shaikh TH. Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation. Genetics. 217. PMID 33724415 DOI: 10.1093/genetics/iyaa038  0.499
2021 Ebert P, Audano PA, Zhu Q, Rodriguez-Martin B, Porubsky D, Bonder MJ, Sulovari A, Ebler J, Zhou W, Serra Mari R, Yilmaz F, Zhao X, Hsieh P, Lee J, Kumar S, et al. Haplotype-resolved diverse human genomes and integrated analysis of structural variation. Science (New York, N.Y.). PMID 33632895 DOI: 10.1126/science.abf7117  0.566
2019 Demaerel W, Mostovoy Y, Yilmaz F, Vervoort L, Pastor S, Hestand MS, Swillen A, Vergaelen E, Geiger EA, Coughlin CR, Chow SK, McDonald-McGinn D, Morrow B, Kwok PY, Xiao M, et al. The 22q11 low copy repeats are characterized by unprecedented size and structural variability. Genome Research. 29: 1389-1401. PMID 31481461 DOI: 10.1101/Gr.248682.119  0.472
2012 Beliveau BJ, Joyce EF, Apostolopoulos N, Yilmaz F, Fonseka CY, McCole RB, Chang Y, Li JB, Senaratne TN, Williams BR, Rouillard JM, Wu CT. Versatile design and synthesis platform for visualizing genomes with Oligopaint FISH probes. Proceedings of the National Academy of Sciences of the United States of America. 109: 21301-6. PMID 23236188 DOI: 10.1073/Pnas.1213818110  0.402
Low-probability matches (unlikely to be authored by this person)
2015 Melia T, Hao P, Yilmaz F, Waxman DJ. Hepatic lincRNAs: high promoter conservation and dynamic, sex-dependent transcriptional regulation by growth hormone. Molecular and Cellular Biology. PMID 26459762 DOI: 10.1128/Mcb.00861-15  0.127
2023 Yilmaz FK, Cakir M, Ikiisik H, Maral I. The Effect of Pneumococcal, Influenza, and COVID-19 Vaccinations on COVID-19 Hospitalization and Progression in People over 65 Years Old Living in Nursing Homes. Vaccines. 11. PMID 37243046 DOI: 10.3390/vaccines11050943  0.12
2022 Bilgin S, Duman TT, Kurtkulagi O, Yilmaz F, Aktas G. A Case of Euglycemic Diabetic Ketoacidosis due to Empagliflozin Use in a Patient with Type 1 Diabetes Mellitus. Journal of the College of Physicians and Surgeons--Pakistan : Jcpsp. 32: 928-930. PMID 35795946 DOI: 10.29271/jcpsp.2022.07.928  0.12
2018 Akdoğan E, Yılmaz FG. The role of acoustic radiation force impulse elastography in the differentiation of benign and malignant focal liver masses. The Turkish Journal of Gastroenterology : the Official Journal of Turkish Society of Gastroenterology. 29: 456-463. PMID 30249561 DOI: 10.5152/tjg.2018.11710  0.12
2015 Kervancioglu S, Yilmaz F. Urgent arterial embolization of ruptured renal angiomyolipoma. Open Medicine (Warsaw, Poland). 10: 233-237. PMID 28352700 DOI: 10.1515/med-2015-0035  0.12
2021 Ikiisik H, Kirlangic M, Turan G, Yilmaz FK, Karayalcin U, Ekiz S, Arikan MA, Gungor FB, Erakkaya ZS, Evirgen B, Maral I. Knowledge and attitude evaluation of physicians and nurses on COVID-19. Northern Clinics of Istanbul. 8: 15-23. PMID 33623868 DOI: 10.14744/nci.2020.82542  0.01
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