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Yagel, Dina
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1

Genetic Markers Among the Israeli Druze Minority Population..:

Shlomovitz, Omer ; Atias-Varon, Danit ; Yagel, Dina...
American Journal of Kidney Diseases.  , 2023
Link: https://doi.org/10.1053/..
 
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2

MO046: Exome sequencing of Israeli Druze individuals on dia..:

Shlomovitz, Omer ; Yagel, Dina ; Barel, Ortal...
Nephrology Dialysis Transplantation.  37 (2022)  Supplement_3 - p. , 2022
Link: https://doi.org/10.1093/..
 
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3

PANGEN: an online platform for the comparison and creation ..:

Isakov, Ofer ; Marek-Yagel, Dina ; Greenberg, Rotem..
Database.  2024 (2024)  - p. , 2024
Link: https://doi.org/10.1093/..
 
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4

Glycogen Storage Disease type IA refractory to cornstarch: ..:

Steg Saban, Or ; Pode-Shakked, Ben ; Abu-Libdeh, Bassam...
European Journal of Medical Genetics.  65 (2022)  6 - p. 104518 , 2022
Link: https://doi.org/10.1016/..
 
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5

Oculocutaneous albinism and bleeding diathesis due to a nov..:

Marek-Yagel, Dina ; Abudi-Sinreich, Shachar ; Macarov, Michal...
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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6

A multidisciplinary nephrogenetic referral clinic for child..:

Pode-Shakked, Ben ; Ben-Moshe, Yishay ; Barel, Ortal...
Pediatric Nephrology.  37 (2022)  7 - p. 1623-1646 , 2022
Link: https://doi.org/10.1007/..
 
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7

Nonsense mutation in the novel PERCC1 gene as a genetic cau..:

Marek-Yagel, Dina ; Stenke, Emily ; Pode-Shakked, Ben...
Human Genetics.  142 (2022)  5 - p. 691-696 , 2022
Link: https://doi.org/10.1007/..
 
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8

A single center experience with publicly funded clinical ex..:

Pode-Shakked, Ben ; Barel, Ortal ; Singer, Amihood...
Scientific Reports.  11 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
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9

Biallelic variants in ETV2 in a family with congenital hear..:

Basel-Salmon, Lina ; Ruhrman-Shahar, Noa ; Barel, Ortal...
European Journal of Medical Genetics.  64 (2021)  2 - p. 104124 , 2021
Link: https://doi.org/10.1016/..
 
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10

Four patients with D-bifunctional protein (DBP) deficiency:..:

Landau, Yuval E. ; Heimer, Gali ; Barel, Ortal...
Molecular Genetics and Metabolism Reports.  25 (2020)  - p. 100631 , 2020
Link: https://doi.org/10.1016/..
 
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11

Progressive Pseudorheumatoid Dysplasia resolved by whole ex..:

Pode-Shakked, Ben ; Vivante, Asaf ; Barel, Ortal...
BMC Medical Genetics.  20 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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12

Noncoding deletions reveal a gene that is critical for inte..:

Oz-Levi, Danit ; Olender, Tsviya ; Bar-Joseph, Ifat...
Nature.  571 (2019)  7763 - p. 107-111 , 2019
Link: https://doi.org/10.1038/..
 
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13

Cerebral and portal vein thrombosis, macrocephaly and atypi..:

Pode-Shakked, Ben ; Heimer, Gali ; Vilboux, Thierry...
Molecular Genetics and Metabolism.  128 (2019)  1-2 - p. 151-161 , 2019
Link: https://doi.org/10.1016/..
 
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14

Genetic and Structural Analysis of a SKIV2L Mutation Causin..:

Vardi, Iddo ; Barel, Ortal ; Sperber, Michal...
Digestive Diseases and Sciences.  63 (2018)  5 - p. 1192-1199 , 2018
Link: https://doi.org/10.1007/..
 
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15

Deleterious variants in TRAK1 disrupt mitochondrial movemen..:

Barel, Ortal ; Malicdan, May Christine V ; Ben-Zeev, Bruria...
Brain.  140 (2017)  3 - p. 568-581 , 2017
Link: https://doi.org/10.1093/..
 
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