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Baris, Hagit N.
196
results:
Search for persons
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Online (196)
Mediatypes
Articles (Online) (127)
Bookchapter (Online) (2)
OpenAccess-fulltext (67)
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1
PI(3,4)P2-mediated cytokinetic abscission prevents early se..:
Gulluni, Federico
;
Prever, Lorenzo
;
Li, Huayi
...
Science. 374 (2021) 6573 - p. , 2021
Link:
https://doi.org/10.1126/..
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2
Identification of a novel PCNT founder pathogenic variant i..:
Weiss, Karin
;
Ekhilevitch, Nina
;
Cohen, Lior
...
European Journal of Medical Genetics. 63 (2020) 2 - p. 103643 , 2020
Link:
https://doi.org/10.1016/..
?
3
Addendum to Letter to the Editor: Safety, efficacy, and aut..:
Mistry, Pramod K.
;
Balwani, Manisha
;
Baris, Hagit N.
...
Blood Cells, Molecules, and Diseases. 77 (2019) - p. 101-102 , 2019
Link:
https://doi.org/10.1016/..
?
4
Mutations in PIK3C2A cause syndromic short stature, skeleta..:
Tiosano, Dov
;
Baris, Hagit N.
;
Chen, Anlu
...
PLOS Genetics. 15 (2019) 4 - p. e1008088 , 2019
Link:
https://doi.org/10.1371/..
?
5
Prenatal microarray analysis in right aortic arch—a retrosp..:
Maya, Idit
;
Singer, Amihood
;
Baris, Hagit N
...
Journal of Perinatology. 38 (2018) 5 - p. 468-473 , 2018
Link:
https://doi.org/10.1038/..
?
6
Microarray analysis in pregnancies with isolated echogenic ..:
Singer, Amihood
;
Maya, Idit
;
Koifman, Arie
...
Early Human Development. 119 (2018) - p. 25-28 , 2018
Link:
https://doi.org/10.1016/..
?
7
Mutations in the mitochondrial ribosomal protein MRPS22 lea..:
Chen, Anlu
;
Tiosano, Dov
;
Guran, Tulay
...
Human Molecular Genetics. 27 (2018) 11 - p. 1913-1926 , 2018
Link:
https://doi.org/10.1093/..
?
8
No Overt Clinical Immunodeficiency Despite Immune Biologica..:
Tesch, Victoria K.
;
IJspeert, Hanna
;
Raicht, Andrea
...
Frontiers in Immunology. 9 (2018) - p. , 2018
Link:
https://doi.org/10.3389/..
?
9
Rare Disease Diagnostics: A Single-center Experience and Le..:
Weiss, Karin
;
Kurolap, Alina
;
Paperna, Tamar
...
Rambam Maimonides Medical Journal. 9 (2018) 3 - p. e0018 , 2018
Link:
https://doi.org/10.5041/..
?
10
Trio approach reveals higher risk of PD in carriers of seve..:
Arkadir, David
;
Dinur, Tama
;
Mullin, Stephen
...
Blood Cells, Molecules, and Diseases. 68 (2018) - p. 115-116 , 2018
Link:
https://doi.org/10.1016/..
?
11
Safety, efficacy, and authorization of eliglustat as a firs..:
Mistry, Pramod K.
;
Balwani, Manisha
;
Baris, Hagit N.
...
Blood Cells, Molecules, and Diseases. 71 (2018) - p. 71-74 , 2018
Link:
https://doi.org/10.1016/..
?
12
Microarray analysis in pregnancies with isolated unilateral..:
Sagi-Dain, Lena
;
Maya, Idit
;
Peleg, Amir
...
Pediatric Research. 83 (2018) 4 - p. 825-828 , 2018
Link:
https://doi.org/10.1038/..
?
13
Constitutional mismatch repair deficiency and Lynch syndrom..:
Abu Freha, Naim
;
Leibovici Weissman, Yaara
;
Fich, Alexander
...
Familial Cancer. 17 (2017) 1 - p. 79-86 , 2017
Link:
https://doi.org/10.1007/..
?
14
Correspondence on "Neurocutaneous Syndromes and Brain Tumor..:
Toledano, Helen
;
Barnes-Kedar, Inbal
;
Baris, Hagit N.
Journal of Child Neurology. 31 (2016) 7 - p. 944-944 , 2016
Link:
https://doi.org/10.1177/..
?
15
Is one diagnosis the whole story? patients with double diag..:
Kurolap, Alina
;
Orenstein, Naama
;
Kedar, Inbal
...
American Journal of Medical Genetics Part A. 170 (2016) 9 - p. 2338-2348 , 2016
Link:
https://doi.org/10.1002/..
1-15