Ruti Parvari

Emailruthibgu.acil

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81 Article
4 Review article
3 Chapter
3 Meeting Abstract
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A novel loss-of-function mutation in MCMDC2 is associated with male infertility
Cohen, O., Abou, F., Waldenberg, N., Gershoni, M., Kleiman, S. E., Parvari, R. & Barak, S., 1 Dec 2026, In: Human Genome Variation. 13, 1, 5.
Research output: Contribution to journal › Article › peer-review

Open Access
Plekhm2 acts as an autophagy modulator in murine heart and cardiofibroblasts
Etzion, S., Hijaze, R., Segal, L., Pilcha, S., Masil, D., Levi, O., Elyagon, S., Levitas, A., Etzion, Y. & Parvari, R., 1 Dec 2024, In: Scientific Reports. 14, 1, 14949.
Research output: Contribution to journal › Article › peer-review

Open Access
1 Scopus citations
A Missense Variation in PHACTR2 Associates with Impaired Actin Dynamics, Dilated Cardiomyopathy, and Left Ventricular Non-Compaction in Humans
Majdalani, P., Levitas, A., Krymko, H., Slanovic, L., Braiman, A., Hadad, U., Dabsan, S., Horev, A., Zarivach, R. & Parvari, R., 1 Jan 2023, In: International Journal of Molecular Sciences. 24, 2, 1388.
Research output: Contribution to journal › Article › peer-review

Open Access
6 Scopus citations
A Novel Mutation in the ADAMTS10 Associated with Weil–Marchesani Syndrome with a Unique Presentation of Developed Membranes Causing Severe Stenosis of the Supra Pulmonic, Supramitral, and Subaortic Areas in the Heart
Levitas, A., Aspit, L., Lowenthal, N., Shaki, D., Krymko, H., Slanovic, L., Yagev, R. & Parvari, R., 1 May 2023, In: International Journal of Molecular Sciences. 24, 10, 8864.
Research output: Contribution to journal › Article › peer-review

Open Access
3 Scopus citations
Functional defects in hiPSCs-derived cardiomyocytes from patients with a PLEKHM2-mutation associated with dilated cardiomyopathy and left ventricular non-compaction
Korover, N., Etzion, S., Cherniak, A., Rabinski, T., Levitas, A., Etzion, Y., Ofir, R., Parvari, R. & Cohen, S., 1 Dec 2023, In: Biological Research. 56, 1, 34.
Research output: Contribution to journal › Article › peer-review

Open Access
6 Scopus citations
Novel Susceptibility Genes Drive Familial Non-Medullary Thyroid Cancer in a Large Consanguineous Kindred
Majdalani, P., Yoel, U., Nasasra, T., Fraenkel, M., Haim, A., Loewenthal, N., Zarivach, R., Hershkovitz, E. & Parvari, R., 1 May 2023, In: International Journal of Molecular Sciences. 24, 9, 8233.
Research output: Contribution to journal › Article › peer-review

Open Access
3 Scopus citations
Dock10 Regulates Cardiac Function under Neurohormonal Stress
Segal, L., Etzion, S., Elyagon, S., Shahar, M., Klapper-Goldstein, H., Levitas, A., Kapiloff, M. S., Parvari, R. & Etzion, Y., 1 Sep 2022, In: International Journal of Molecular Sciences. 23, 17, 9616.
Research output: Contribution to journal › Article › peer-review

Open Access
4 Scopus citations
Ocular manifestations among patients with congenital insensitivity to pain due to variants in PRDM12 and SCN9A genes
Elsana, B., Imtirat, A., Yagev, R., Gradstein, L., Majdalani, P., Iny, O., Parvari, R. & Tsumi, E., 1 Dec 2022, In: American Journal of Medical Genetics, Part A. 188, 12, p. 3463-3468 6 p.
Research output: Contribution to journal › Article › peer-review

Open Access
5 Scopus citations
Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity
Faingelernt, Y., Hershkovitz, E., Abu-Libdeh, B., Abedrabbo, A., Abu-Rmaileh Amro, S., Zarivach, R., Zangen, D., Lavi, E., Haim, A., Parvari, R. & Abu-Libdeh, A., 1 Apr 2021, In: American Journal of Medical Genetics, Part A. 185, 4, p. 1033-1038 6 p.
Research output: Contribution to journal › Article › peer-review
5 Scopus citations
Mutation in CATIP (C2orf62) causes oligoteratoasthenozoospermia by affecting actin dynamics
Arafat, M., Harlev, A., Har-Vardi, I., Levitas, E., Priel, T., Gershoni, M., Searby, C., Sheffield, V. C., Lunenfeld, E. & Parvari, R., 1 Feb 2021, In: Journal of Medical Genetics. 58, 2, p. 106-115 10 p.
Research output: Contribution to journal › Article › peer-review
13 Scopus citations

3 Active
4 Finished

Genes in left-right body asymetry
Parvari, R. (PI), Reish, O. (CoPI) & Sheffield, V. C. (CoPI)
1/01/11 → …
Project: Research
Genes in left-right body asymetry
Parvari, R. (PI), Reish, O. (CoPI) & Sheffield, V. C. (CoPI)
United States-Israel Binational Science Foundation (BSF)
1/01/11 → …
Project: Research
Study the Cellular Functions of Tubulin Chaperone E
Parvari, R. (PI) & Diaz, G. (CoPI)
United States-Israel Binational Science Foundation (BSF)
1/01/05 → …
Project: Research
Study of the genetic basis of male infertility
Parvari, R. (PI) & E Kleiman, S. S. (CoPI)
Israel Science Foundation
1/01/21 → 31/12/24
Project: Research
Plekhm2, a newly identified autophagy modulator, associated with familial dilated cardiomyopathy
Parvari, R. (PI) & Etzion, S. (CoPI)
Israel Science Foundation
1/01/16 → 31/12/19
Project: Research
Identification and characterization of the mutations causing recessive Primary Ciliary Dyskinesia in the population of the Bedouins of the Negev
Parvari, R. (PI)
Israel Science Foundation
1/01/10 → 31/12/12
Project: Research
Study of a new putative methyltransferase gene deleted in patients with cystinuria, retardation and mitochondrial disease
Parvari, R. (PI) & Hershkovitz, E. (CoPI)
Israel Science Foundation
1/01/05 → 31/12/08
Project: Research

Ruti Parvari

Personal profile

Fingerprint

Collaborations and top research areas from the last five years

Dive into details

A novel loss-of-function mutation in MCMDC2 is associated with male infertility

Plekhm2 acts as an autophagy modulator in murine heart and cardiofibroblasts

A Missense Variation in PHACTR2 Associates with Impaired Actin Dynamics, Dilated Cardiomyopathy, and Left Ventricular Non-Compaction in Humans

A Novel Mutation in the ADAMTS10 Associated with Weil–Marchesani Syndrome with a Unique Presentation of Developed Membranes Causing Severe Stenosis of the Supra Pulmonic, Supramitral, and Subaortic Areas in the Heart

Functional defects in hiPSCs-derived cardiomyocytes from patients with a PLEKHM2-mutation associated with dilated cardiomyopathy and left ventricular non-compaction

Novel Susceptibility Genes Drive Familial Non-Medullary Thyroid Cancer in a Large Consanguineous Kindred

Dock10 Regulates Cardiac Function under Neurohormonal Stress

Ocular manifestations among patients with congenital insensitivity to pain due to variants in PRDM12 and SCN9A genes

Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity

Mutation in CATIP (C2orf62) causes oligoteratoasthenozoospermia by affecting actin dynamics

Genes in left-right body asymetry

Genes in left-right body asymetry

Study the Cellular Functions of Tubulin Chaperone E

Study of the genetic basis of male infertility

Plekhm2, a newly identified autophagy modulator, associated with familial dilated cardiomyopathy

Identification and characterization of the mutations causing recessive Primary Ciliary Dyskinesia in the population of the Bedouins of the Negev

Study of a new putative methyltransferase gene deleted in patients with cystinuria, retardation and mitochondrial disease

Ruti Parvari

Personal profile

Fingerprint

Collaborations and top research areas from the last five years

Research output

Projects