Hadid Y - Search Results

1

Danon Disease: Entire LAMP2 Gene Deletion with Unusual Clinical Presentation-Case Report and Review of the Literature.

Shalata A, Bar-Shai M, Hadid Y, Mahroum M, Mintz H, Shalata ZE, Radzishevsky E, Genizi J, Lorber A, Ben-Yosef T, Yaniv L. Shalata A, et al. Among authors: hadid y. Genes (Basel). 2023 Jul 27;14(8):1539. doi: 10.3390/genes14081539. Genes (Basel). 2023. PMID: 37628591 Free PMC article. Review.

2

Performance of CellDetect for detection of bladder cancer: Comparison with urine cytology and UroVysion.

Shefer HK, Masarwe I, Bejar J, Naamnih LH, Gueta-Milshtein K, Shalata A, Hadid Y, Nativ O, Nativ O. Shefer HK, et al. Among authors: hadid y. Urol Oncol. 2023 Jun;41(6):296.e1-296.e8. doi: 10.1016/j.urolonc.2022.12.012. Epub 2023 Jan 14. Urol Oncol. 2023. PMID: 36642638

3

[IDENTIFICATION OF A NOVEL LTBP3 GENE PATHOGENIC VARIANT IN DRUZE ARAB PATIENTS PRESENTED WITH SYNDROMIC SHORT STATURE WITH BRACHYOLMIA AND AMELOGENESIS IMPERFECTA].

Hadid Y, Daher Z, Mahroum M, Shalata A, Nakhleh Francis Y, Shalata H, Broneshter Vinter R, Ziv M, Furman C, Ali V, Levitaz J, Shalata A. Hadid Y, et al. Harefuah. 2023 Jun;162(6):352-358. Harefuah. 2023. PMID: 37394436 Hebrew.

4

Biallelic mutations in EXOC3L2 cause a novel syndrome that affects the brain, kidney and blood.

Shalata A, Lauhasurayotin S, Leibovitz Z, Li H, Hebert D, Dhanraj S, Hadid Y, Mahroum M, Bajar J, Egenburg S, Arad A, Shohat M, Haddad S, Bakry H, Moshiri H, Scherer SW, Tzur S, Dror Y. Shalata A, et al. Among authors: hadid y. J Med Genet. 2019 May;56(5):340-346. doi: 10.1136/jmedgenet-2018-105421. Epub 2018 Oct 16. J Med Genet. 2019. PMID: 30327448

5

Explainable machine learning for chronic lymphocytic leukemia treatment prediction using only inexpensive tests.

Meiseles A, Paley D, Ziv M, Hadid Y, Rokach L, Tadmor T. Meiseles A, et al. Among authors: hadid y. Comput Biol Med. 2022 Jun;145:105490. doi: 10.1016/j.compbiomed.2022.105490. Epub 2022 Apr 6. Comput Biol Med. 2022. PMID: 35405402

6

Identification of a novel PCNT founder pathogenic variant in the Israeli Druze population.

Weiss K, Ekhilevitch N, Cohen L, Bratman-Morag S, Bello R, Martinez AF, Hadid Y, Shlush LI, Kurolap A, Paperna T, Mory A, Baris HN, Muenke M. Weiss K, et al. Among authors: hadid y. Eur J Med Genet. 2020 Feb;63(2):103643. doi: 10.1016/j.ejmg.2019.03.007. Epub 2019 Mar 25. Eur J Med Genet. 2020. PMID: 30922925

7

Non-visualization of fetal gallbladder in microarray era - a retrospective cohort study and review of the literature.

Sagi-Dain L, Singer A, Hadid Y, Sharony R, Vinkler C, Bar-Shira A, Segel R, Ben Shachar S, Maya I. Sagi-Dain L, et al. Among authors: hadid y. J Matern Fetal Neonatal Med. 2019 Aug;32(16):2643-2648. doi: 10.1080/14767058.2018.1443070. Epub 2018 Feb 28. J Matern Fetal Neonatal Med. 2019. PMID: 29455582 Review.

8

The Druze: a population genetic refugium of the Near East.

Shlush LI, Behar DM, Yudkovsky G, Templeton A, Hadid Y, Basis F, Hammer M, Itzkovitz S, Skorecki K. Shlush LI, et al. Among authors: hadid y. PLoS One. 2008 May 7;3(5):e2105. doi: 10.1371/journal.pone.0002105. PLoS One. 2008. PMID: 18461126 Free PMC article.

9

The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event.

Behar DM, Metspalu E, Kivisild T, Achilli A, Hadid Y, Tzur S, Pereira L, Amorim A, Quintana-Murci L, Majamaa K, Herrnstadt C, Howell N, Balanovsky O, Kutuev I, Pshenichnov A, Gurwitz D, Bonne-Tamir B, Torroni A, Villems R, Skorecki K. Behar DM, et al. Among authors: hadid y. Am J Hum Genet. 2006 Mar;78(3):487-97. doi: 10.1086/500307. Epub 2006 Jan 11. Am J Hum Genet. 2006. PMID: 16404693 Free PMC article.

10

A novel 154-bp deletion in the human mitochondrial DNA control region in healthy individuals.

Behar DM, Blue-Smith J, Soria-Hernanz DF, Tzur S, Hadid Y, Bormans C, Moen A, Tyler-Smith C, Quintana-Murci L, Wells RS; Genographic Consortium. Behar DM, et al. Among authors: hadid y. Hum Mutat. 2008 Dec;29(12):1387-91. doi: 10.1002/humu.20835. Hum Mutat. 2008. PMID: 18629826 Free PMC article.

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