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Kol, Nitzan
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1

RIPK1 mutations causing infantile-onset IBD with inflammato..:

Sultan, Mutaz ; Adawi, Mohammad ; Kol, Nitzan...
Frontiers in Immunology.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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2

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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3

524: PATHOGENIC RIPK1 MUTATIONS CAUSE INFANTILE-ONSET IBD W..:

Sultan, Mutaz ; Wilschanski, Michael ; Millman, Peri...
Gastroenterology.  162 (2022)  7 - p. S-121-S-122 , 2022
Link: https://doi.org/10.1016/..
 
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4

Remodeling of the m6A RNA landscape in the conversion of ac..:

Bueno-Costa, Alberto ; Piñeyro, David ; García-Prieto, Carlos A....
Leukemia.  36 (2022)  8 - p. 2121-2124 , 2022
Link: https://doi.org/10.1038/..
 
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5

SurviveAI: Long Term Survival Prediction of Cancer Patients..:

Nayshool, Omri ; Kol, Nitzan ; Javaski, Elisheva..
Cancer Informatics.  21 (2022)  - p. 117693512211278 , 2022
Link: https://doi.org/10.1177/..
 
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6

Dynamic regulation of N6,2′-O-dimethyladenosine (m6Am) in o..:

Ben-Haim, Moshe Shay ; Pinto, Yishay ; Moshitch-Moshkovitz, Sharon...
Nature Communications.  12 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
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7

Transcriptomic profiling and genomic mutational analysis of..:

Friedman, Nehemya ; Jacob-Hirsch, Jasmine ; Drori, Yaron...
PLOS ONE.  16 (2021)  2 - p. e0247128 , 2021
Link: https://doi.org/10.1371/..
 
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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

Correction to: ESR1 mutations are frequent in newly diagnos..:

Zundelevich, Adi ; Dadiani, Maya ; Kahana-Edwin, Smadar...
Breast Cancer Research.  22 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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10

Whole exome sequencing (WES) approach for diagnosing primar..:

Simon, Amos J. ; Golan, Adi Cohen ; Lev, Atar...
Clinical Immunology.  214 (2020)  - p. 108376 , 2020
Link: https://doi.org/10.1016/..
 
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11

ESR1 mutations are frequent in newly diagnosed metastatic a..:

Zundelevich, Adi ; Dadiani, Maya ; Kahana-Edwin, Smadar...
Breast Cancer Research.  22 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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12

Identification of a homozygousVRK1mutation in two patients ..:

Greenbaum, Lior ; Barel, Ortal ; Nikitin, Vera...
Muscle & Nerve.  61 (2020)  3 - p. 395-400 , 2020
Link: https://doi.org/10.1002/..
 
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13

A founder truncating variant in GDF1 causes autosomal‐reces..:

Marek‐Yagel, Dina ; Bolkier, Yoav ; Barel, Ortal...
American Journal of Medical Genetics Part A.  182 (2020)  5 - p. 987-993 , 2020
Link: https://doi.org/10.1002/..
 
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14

Netrin‐G2 dysfunction causes a Rett‐like phenotype with are..:

Heimer, Gali ; Woerden, Geeske M. ; Barel, Ortal...
Human Mutation.  41 (2019)  2 - p. 476-486 , 2019
Link: https://doi.org/10.1002/..
 
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15

MEDU-30. IDENTIFYING DISTINCTIVE lincRNAs IN THE DIFFERENT ..:

Freedman, Shany ; Yalon, Michal ; Eyal, Eran...
Neuro-Oncology.  21 (2019)  Supplement_2 - p. ii109-ii109 , 2019
Link: https://doi.org/10.1093/..
 
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