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Year Number of Results
2019 1
2020 6
2021 3
2022 5
2024 0

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12 results

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Page 1
An overview of the genetic aspects of hair loss and its connection with nutrition.
Gokce N, Basgoz N, Kenanoglu S, Akalin H, Ozkul Y, Ergoren MC, Beccari T, Bertelli M, Dundar M. Gokce N, et al. Among authors: kenanoglu s. J Prev Med Hyg. 2022 Oct 17;63(2 Suppl 3):E228-E238. doi: 10.15167/2421-4248/jpmh2022.63.2S3.2765. eCollection 2022 Jun. J Prev Med Hyg. 2022. PMID: 36479473 Free PMC article. Review.
Implication of the Mediterranean diet on the human epigenome.
Kenanoglu S, Gokce N, Akalin H, Ergoren MC, Beccari T, Bertelli M, Dundar M. Kenanoglu S, et al. J Prev Med Hyg. 2022 Oct 17;63(2 Suppl 3):E44-E55. doi: 10.15167/2421-4248/jpmh2022.63.2S3.2746. eCollection 2022 Jun. J Prev Med Hyg. 2022. PMID: 36479488 Free PMC article. Review.
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Dundar M, Fahrioglu U, Yildiz SH, Bakir-Gungor B, Temel SG, Akin H, Artan S, Cora T, Sahin FI, Dursun A, Sezer O, Gurkan H, Erdogan M, Gunduz CNS, Bisgin A, Ozdemir O, Ulgenalp A, Percin EF, Yildirim ME, Tekes S, Bagis H, Yuce H, Duman N, Bozkurt G, Yararbas K, Yildirim MS, Arman A, Mihci E, Eraslan S, Altintas ZM, Aymelek HS, Ruhi HI, Tatar A, Ergoren MC, Cetin GO, Altunoglu U, Caglayan AO, Yuksel B, Ozkul Y, Saatci C, Kenanoglu S, Karasu N, Dundar B, Ozcelik F, Demir M, Siniksaran BS, Kulak H, Kiranatlioglu K, Baysal K, Kazimli U, Akalin H, Dundar A, Boz M, Bayram A, Subasioglu A, Colak FK, Karaduman N, Gunes MC, Kandemir N, Aynekin B, Emekli R, Sahin IO, Ozdemir SY, Onal MG, Senel AS, Poyrazoglu MH, Kisaarslan ANP, Gursoy S, Baskol M, Calis M, Demir H, Zararsiz GE, Erdogan MO, Elmas M, Solak M, Ulu MS, Thahir A, Aydin Z, Atasever U, Sag SO, Aliyeva L, Alemdar A, Dogan B, Erguzeloglu CO, Kaya N, Ozkinay F, Cogulu O, Durmaz A, Onay H, Karaca E, Durmaz B, Aykut A, Cilingir O, Aras BD, Gokalp EE, Arslan S, Temena A, Haziyeva K, Kocagil S, Bas H, Susam E, Keklikci AR, Sarac E, Kocak N, Nergiz S, Terzi YK, Dincer SA, Baskin ES, Genc GC, Bahadir O, Sanri A, Yigit S, Tozkir H, Y… See abstract for full author list ➔ Dundar M, et al. Among authors: kenanoglu s. Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3. Epub 2022 Jan 31. Funct Integr Genomics. 2022. PMID: 35098403
Possible Role of the RORC Gene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative Variants.
Michelini S, Ricci M, Serrani R, Stuppia L, Beccari T, Veselenyiova D, Kenanoglu S, Barati S, Kurti D, Baglivo M, Basha SH, Krajcovic J, Dundar M, Bertelli M. Michelini S, et al. Among authors: kenanoglu s. Lymphat Res Biol. 2021 Apr;19(2):129-133. doi: 10.1089/lrb.2020.0030. Epub 2020 Sep 22. Lymphat Res Biol. 2021. PMID: 32960152 Review.
TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema.
Michelini S, Ricci M, Veselenyiova D, Kenanoglu S, Kurti D, Baglivo M, Fiorentino A, Basha SH, Priya S, Serrani R, Krajcovic J, Dundar M, Dautaj A, Bertelli M. Michelini S, et al. Among authors: kenanoglu s. Int J Mol Sci. 2020 Sep 16;21(18):6780. doi: 10.3390/ijms21186780. Int J Mol Sci. 2020. PMID: 32947856 Free PMC article.
CDH5, a Possible New Candidate Gene for Genetic Testing of Lymphedema.
Michelini S, Ricci M, Amato B, Gentileschi S, Veselenyiova D, Kenanoglu S, Fiorentino A, Kurti D, Baglivo M, Manara E, Basha SH, Priya S, Krajcovic J, Dundar M, Belgrado JP, Dautaj A, Bertelli M. Michelini S, et al. Among authors: kenanoglu s. Lymphat Res Biol. 2022 Oct;20(5):496-506. doi: 10.1089/lrb.2020.0089. Epub 2021 Dec 8. Lymphat Res Biol. 2022. PMID: 34882481
Two rare PROX1 variants in patients with lymphedema.
Ricci M, Amato B, Barati S, Compagna R, Veselenyiova D, Kenanoglu S, Stuppia L, Beccari T, Baglivo M, Kurti D, Krajcovic J, Serrani R, Dundar M, Basha SH, Chiurazzi P, Bertelli M. Ricci M, et al. Among authors: kenanoglu s. Mol Genet Genomic Med. 2020 Oct;8(10):e1424. doi: 10.1002/mgg3.1424. Epub 2020 Aug 5. Mol Genet Genomic Med. 2020. PMID: 32757260 Free PMC article.
Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema.
Michelini S, Amato B, Ricci M, Kenanoglu S, Veselenyiova D, Kurti D, Baglivo M, Manara E, Dundar M, Krajcovic J, Basha SH, Priya S, Serrani R, Miggiano GAD, Aquilanti B, Matera G, Velluti V, Gagliardi L, Dautaj A, Bertelli M. Michelini S, et al. Among authors: kenanoglu s. Genes (Basel). 2020 Nov 17;11(11):1361. doi: 10.3390/genes11111361. Genes (Basel). 2020. PMID: 33212964 Free PMC article.
NOTCH1: Review of its role in lymphatic development and study of seven families with rare pathogenic variants.
Michelini S, Ricci M, Serrani R, Barati S, Kenanoglu S, Veselenyiova D, Kurti D, Baglivo M, Basha SH, Priya S, Dautaj A, Dundar M, Krajcovic J, Bertelli M. Michelini S, et al. Among authors: kenanoglu s. Mol Genet Genomic Med. 2021 Jan;9(1):e1529. doi: 10.1002/mgg3.1529. Epub 2020 Nov 28. Mol Genet Genomic Med. 2021. PMID: 33247628 Free PMC article.
12 results