1. Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity. Issue 3 (6th November 2015) Authors: Baris, Hagit N.; Barnes‐Kedar, Inbal; Toledano, Helen; Halpern, Marisa; Hershkovitz, Dov; Lossos, Alexander; Lerer, Israela; Peretz, Tamar; Kariv, Revital; Cohen, Shlomi; Half, Elizabeth E.; Magal, Nurit; Drasinover, Valerie; Wimmer, Katharina; Goldberg, Yael; Bercovich, Dani; Levi, Zohar Journal: Pediatric blood & cancer Issue: Volume 63:Issue 3(2016) Page Start: 418 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder. (15th July 2015) Authors: Lossos, Alexander; Elazar, Nimrod; Lerer, Israela; Schueler-Furman, Ora; Fellig, Yakov; Glick, Benjamin; Zimmerman, Bat-El; Azulay, Haim; Dotan, Shlomo; Goldberg, Sharon; Gomori, John M.; Ponger, Penina; Newman, J. P.; Marreed, Hodaifah; Steck, Andreas J.; Schaeren-Wiemers, Nicole; Mor, Nofar; Ha... Journal: Brain Issue: Volume 138:Part 9(2015:Sep.) Page Start: 2521 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. MYORG is associated with recessive primary familial brain calcification. Issue 1 (15th November 2018) Authors: Arkadir, David; Lossos, Alexander; Rahat, Dolev; Abu Snineh, Muneer; Schueler‐Furman, Ora; Nitschke, Silvia; Minassian, Berge A.; Sadaka, Yair; Lerer, Israela; Tabach, Yuval; Meiner, Vardiella Journal: Annals of clinical and translational neurology Issue: Volume 6:Issue 1(2019) Page Start: 106 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Ultrasound findings provide clues to investigate founder mutations expressed as runs of homozygosity in chromosomal microarray studies. (19th January 2018) Authors: Daum, Hagit; Lerer, Israela; Frumkin, Ayala; Rosenak, Daniel; Yanai, Nili; Porat, Shay; Yagel, Simcha; Meiner, Vardiella Journal: Prenatal diagnosis Issue: Volume 38:Number 2(2018) Page Start: 135 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗