Ruti Parvari

4.1k citations
90 papers · 2.9k · h-index 28

Impact in

Papers in

  • Molecular Biology 49
    • Congenital heart defects research 9
    • RNA modifications and cancer 7
  • Genetics 20
    • Genetics and Neurodevelopmental Disorders 8
Co-authors
Eli Hershkovitz (27 shared papers)Shimon Moses (15 shared papers)Val C. Sheffield (11 shared papers)Moshe Phillip (4 shared papers)Jonathan Eli Arbelle (3 shared papers)Yael Segev (3 shared papers)Esther Manor (7 shared papers)Vered Chalifa‐Caspi (5 shared papers)
Journals
European Journal of Human Genetics (6 papers)The American Journal of Human Genetics (5 papers)Journal of Inherited Metabolic Disease (4 papers)International Journal of Molecular Sciences (4 papers)Proceedings of the National Academy of Sciences (3 papers)
Partner nations
IsraelUnited StatesHungary

In The Last Decade

Ruti Parvari

89 papers receiving 2.8k citations

Peers

Ruti Parvari
Comparison fields: 5 of 116
  • Reproductive Medicine 270
  • Rheumatology 448
  • Nephrology 198
  • Genetics 770
  • Cellular and Molecular Neuroscience 327
Replace Thomas B. Thompson with:
Thomas B. Thompson United States
Patricia M. Zerfas United States
Dani Bercovich Israel
Siu Yuen Chan Hong Kong
Nancy E. Cooke United States
Ohad S. Birk Israel
Miguel Chillón Spain
Jiro Takahara Japan
Pnina Fishman Israel
Lincoln R. Potter United States
Ruti Parvari relative to Thomas B. Thompson United States Thomas B. Thompson's profile →
Citations per field
00.5×2×3×4×4.6×
Thomas B. Thompson · 1×
Citations per year

Countries citing papers authored by Ruti Parvari

Since Specialization
Citations

This map shows the geographic impact of Ruti Parvari's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ruti Parvari with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruti Parvari more than expected).

Fields of papers citing papers by Ruti Parvari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ruti Parvari. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ruti Parvari. The network helps show where Ruti Parvari may publish in the future.

Co-authors

The 25 scholars most cited alongside Ruti Parvari, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ruti Parvari Line = papers co-authored together Ruti Parvari links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 90 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Autosomal-Recessive Hypophosphatemic Rickets Is Associated with an Inactivation Mutation in the ENPP1 Gene
The American Journal of Human Genetics ·Varda Levy-Litan, Eli Hershkovitz, Luba Avizov, Neta Leventhal, Dani Bercovich, Vered Chalifa‐Caspi, Esther Manor, Sophia Buriakovsky, Yair Hadad, James W. Goding, Ruti Parvari
2010207
2
Mutation of TBCE causes hypoparathyroidism– retardation–dysmorphism and autosomal recessive Kenny–Caffey syndrome
Nature Genetics ·Ruti Parvari, Rafael Gorodischer, Eli Hershkovitz, Nili Grossman, Bart Loeys, Geert Mortier, Alexandra Zecic, Simon G. Gregory, Reuven Sharony, Nadia Sakati, Abdul Karim Al Humaidan, Fatma Al Zanhrani, Brian F. Meyer, Aida I. Al Aqeel, Marios Kambouris, Abdulrahman Swaid, Johara Al Othman, (unknown), Bruce D. Gelb, Rory B. Weiner, (unknown)
2002167
3
Male Hypogonadism Due to a Mutation in the Gene for the β-Subunit of Follicle-Stimulating Hormone
New England Journal of Medicine ·Moshe Phillip, Jonathan Eli Arbelle, Yael Segev, Ruti Parvari
1998164
4
Linkage of Bardet–Biedl syndrome to chromosome 16q and evidence for non–allelic genetic heterogeneity
Nature Genetics ·Anne E. Kwitek, Rivka Carmi, Geoffrey M. Duyk, Kenneth H. Buetow, Khalil Elbedour, Ruti Parvari, Chandra Naidu Yandava, Edwin M. Stone, Val C. Sheffield
1993134
5
Chicken immunoglobulin gamma‐heavy chains: limited VH gene repertoire, combinatorial diversification by D gene segments and evolution of the heavy chain locus.
The EMBO Journal ·Ruti Parvari, Aaron Avivi, F. Lentner, Etty Ziv, Shoshana Tel‐Or, Yigal Burstein, Israël Schechter
1988130
6
The Variable Presentations of Glycogen Storage Disease Type IV: A Review of Clinical, Enzymatic and Molecular Studies
Current Molecular Medicine ·Shimon Moses, Ruti Parvari
2002109
7
Mutation in TDRD9 causes non-obstructive azoospermia in infertile men
Journal of Medical Genetics ·Maram Arafat, Iris Har‐Vardi, Avi Harlev, Eliahu Levitas, Atif Zeadna, Maram Abofoul‐Azab, Victor Dyomin, Val C. Sheffield, Eitan Lunenfeld, Mahmoud Huleihel, Ruti Parvari
2017103
8
Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: Genetic heterogeneity, novel mutations in theTRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies
American Journal of Medical Genetics ·Sharon Shatzky, Shimon Moses, Jacov Levy, Vered Pinsk, Eli Hershkovitz, L. Herzog, Zamir Shorer, Anthony Luder, Ruti Parvari
2000101
9
The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23
The American Journal of Human Genetics ·Borhane Annabi, Brian C. Mansfield, Hisayuki Hiraiwa, Ke-Jian Lei, Tsuneyuki Ubagai, Mihael H. Polymeropoulos, Shimon Moses, Ruti Parvari, Eli Hershkovitz, Hanna Mandel, Moshe Fryman, Janice Y. Chou
199892
10
Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase
European Journal of Human Genetics ·Aviva Levitas, Emad Muhammad, Gali Harel, Ann Saada, Vered Chalifa‐Caspi, Esther Manor, John C. Beck, Val C. Sheffield, Ruti Parvari
201089
11
Primary Ciliary Dyskinesia Caused by Homozygous Mutation in DNAL1, Encoding Dynein Light Chain 1
The American Journal of Human Genetics ·M. Mazor, Soliman Alkrinawi, Vered Chalifa‐Caspi, Esther Manor, Val C. Sheffield, Micha Aviram, Ruti Parvari
201189
12
Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations
Human Mutation ·James J. Cox, Jony Sheynin, Zamir Shorer, Frank Reimann, Adeline K. Nicholas, Lorena Zubović, Marco Baralle, Elizabeth Wraige, Esther Manor, Jacov Levy, Crislyn Woods, Ruti Parvari
201085
13
Congenital insensitivity to pain: Orthopaedic manifestations
Journal of Bone and Joint Surgery - British Volume ·Elhanan Bar‐On, D. Weigl, Ruti Parvari, Kalman Katz, Raphael Weitz, Tamar Steinberg
200270
14
Male Hypogonadism Due to a Mutation in the Gene for the beta-Subunit of Follicle-Stimulating Hormone
The Journal of Urology ·Moshe Phillip, Jonathan Eli Arbelle, Yael Segev, Ruti Parvari
199968
15
A microfluorometric assay for cholinesterases, suitable for multiple kinetic determinations of picomoles of released thiocholine
Analytical Biochemistry ·Ruti Parvari, Israel Pecht, Hermona Soreq
198362
16
PLEKHM2mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction
Human Molecular Genetics ·Emad Muhammad, Aviva Levitas, Sonia R. Singh, Alex Braiman, Rivka Ofir, Sharon Etzion, Val C. Sheffield, Yoram Etzion, Lucie Carrier, Ruti Parvari
201559
17
A Single-Base Deletion in the 3'-Coding Region of Glycogen-Debranching Enzyme Is Prevalent in Glycogen Storage Disease Type IIIA in a Population of North African Jewish Patients
European Journal of Human Genetics ·Ruti Parvari, Shimon Moses, Jianjun Shen, Eli Hershkovitz, Aaron Lerner, Yuan-Tsong Chen
199752
18
Somatic diversification of chicken immunoglobulin light chains by point mutations.
Proceedings of the National Academy of Sciences ·Ruti Parvari, Etty Ziv, Frida Lantner, Debra S. Heller, Israël Schechter
199049
19
Homozygosity and Linkage-Disequilibrium Mapping of the Syndrome of Congenital Hypoparathyroidism, Growth and Mental Retardation, and Dysmorphism to a 1-cM Interval on Chromosome 1q42-43
The American Journal of Human Genetics ·Ruti Parvari, Eli Hershkovitz, Adam B. Kanis, Rafael Gorodischer, Shlomit Shalitin, Val C. Sheffield, Rivka Carmi
199846
20
Biosynthesis and secretion of catalytically active acetylcholinesterase in Xenopus oocytes microinjected with mRNA from rat brain and from Torpedo electric organ.
Proceedings of the National Academy of Sciences ·Hermona Soreq, Ruti Parvari, Israel Silman
198245

About Ruti Parvari

Ruti Parvari is a scholar working on Molecular Biology, Genetics, Rheumatology, Cardiology and Cardiovascular Medicine and Surgery, having authored 90 papers that have together received 2.9k indexed citations. Recurring topics across this work include Glycogen Storage Diseases and Myoclonus (11 papers), Cardiomyopathy and Myosin Studies (11 papers), Congenital heart defects research (9 papers), Carbohydrate Chemistry and Synthesis (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Lysosomal Storage Disorders Research (7 papers), RNA modifications and cancer (7 papers) and Folate and B Vitamins Research (4 papers). The work is most often cited by research in Reproductive Medicine (270 citations), Rheumatology (448 citations), Nephrology (198 citations), Genetics (770 citations) and Cellular and Molecular Neuroscience (327 citations). Ruti Parvari has collaborated with scholars based in Israel, United States and Hungary. Frequent co-authors include Eli Hershkovitz, Shimon Moses, Val C. Sheffield, Moshe Phillip, Jonathan Eli Arbelle, Yael Segev, Esther Manor, Vered Chalifa‐Caspi, Rivka Carmi and Aviva Levitas. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Journal of Inherited Metabolic Disease, International Journal of Molecular Sciences and Proceedings of the National Academy of Sciences.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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