Ruth Bargal

1.6k citations

29 papers · 1.2k indexed · h-index 17

Impact in

Physiology top 0.2%
- Calcium signaling and nucleotide metabolism
- Lysosomal Storage Disorders Research
- Adenosine and Purinergic Signaling
Sensory Systems top 2%
- Ion Channels and Receptors

Papers in

Physiology 14
- Lysosomal Storage Disorders Research 15
- Calcium signaling and nucleotide metabolism 14
- Adenosine and Purinergic Signaling 3
Cell Biology 7
- Cellular transport and secretion 7

Co-authors: Gideon Bach Annick Raas‐Rothschild Marcia Zeigler Nili Avidan Ayala Frumkin Gustavo Glusman Doron Lancet Edna Ben‐Asher
Journals: Human Mutation (4 papers)Journal of Inherited Metabolic Disease (2 papers)Prenatal Diagnosis (2 papers)Journal of the American Academy of Dermatology (1 paper)Nature Medicine (1 paper)
Partner nations: Israel United States France

In The Last Decade

Ruth Bargal

29 papers receiving 1.2k citations

Peers

Countries citing papers authored by Ruth Bargal

Since Specialization

Citations

This map shows the geographic impact of Ruth Bargal'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 Ruth Bargal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruth Bargal more than expected).

Fields of papers citing papers by Ruth Bargal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ruth Bargal. 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 Ruth Bargal. The network helps show where Ruth Bargal may publish in the future.

Co-authors

The 25 scholars most cited alongside Ruth Bargal, 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 Ruth Bargal Line = papers co-authored together Ruth Bargal links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A novel SCARB2 mutation in progressive myoclonus epilepsy indicated by reduced β-glucocerebrosidase activity Journal of the Neurological Sciences ·Marsha Zeigler, Vardiella Meiner, J. P. Newman, Bettina Steiner‐Birmanns, Ruth Bargal, 一昊朴, Лилия Семеновна Хорошилова, Or Kakhlon, Jouko Mehtäläinen, Zohar Argov, Oded Abramsky, Alexander Lossos	2014	18
2	Hyperargininemia: A Family with a Novel Mutation in an Unexpected Site JIMD Reports ·Yoni Cohen, Ruth Bargal, M. Zeigler, Gu HY, Wendy A. Petow, Avraham Zeharia	2011	12
3	Genetic screening for Krabbe disease: Learning from the past and looking to the future American Journal of Medical Genetics Part A ·Khampoun Sayasith, Joël Zlotogora, Vardiella Meiner, Hong He, 一昊朴, Лилия Семеновна Хорошилова, Ruth Bargal, 豊造原田, 葛晨霞, Marsha Zeigler	2011	7
4	Origin and spread of a common deletion causing mucolipidosis type II: insights from patterns of haplotypic diversity Clinical Genetics ·Maria Francisca Coutinho, Marisa Encarnação, T. Carlyle, 啓暁水原, Sandra Martins, Tongyang Xu, Ruth Bargal, Mirella Filocamo, Annick Raas‐Rothschild, Barbara Tappino, Catherine Laprise, Pengshan Chang, Navarro Lisowski, Osvaldo Artigalás, Maria João Prata, Sandra Alves	2010	12
5	The clinical spectrum of fetal Niemann–Pick type C American Journal of Medical Genetics Part A ·Ronen Spiegel, Annick Raas‐Rothschild, Orit Reish, Ryokichi Tokunaga, Vardiella Meiner, Ruth Bargal, 一昊朴, Karen Meir, Michel Nadjari, Gratiana Hermann, DV Swetland, Stavit A. Shalev, Marsha Zeigler	2009	68
6	Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications The American Journal of Human Genetics ·Ruth Bargal, Valérie Cormier‐Daire, Ziva Ben‐Neriah, Martine Le Merrer, Jacob Sosna, Judith Melki, David Zangen, Sarah Smithson, Zvi Borochowitz, Ruth Belostotsky, Annick Raas‐Rothschild	2008	82
7	P35S mutation in the NOG gene associated with Teunissen–Cremers syndrome and features of multiple NOG joint-fusion syndromes European Journal of Medical Genetics ·Nir Hirshoren, Menachem Gross, Eyal Banin, Jacob Sosna, Ruth Bargal, Annick Raas‐Rothschild	2008	20
8	Angiokeratoma corporis diffusum in human β-mannosidosis: Report of a new case and a novel mutation Journal of the American Academy of Dermatology ·Vered Molho‐Pessach, Ruth Bargal, João Reis Costa Mendes, Victoria Doviner, Arieh Ingber, Annick Raas‐Rothschild, Zvi Neʼeman, Marsha Zeigler, Abraham Zlotogorski	2007	15
9	When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patients Molecular Genetics and Metabolism ·Ruth Bargal, Marsha Zeigler, Bassam Abu‐Libdeh, Wendy A. Petow, Hanna Mandel, Ziva Ben Neriah, Fiona Stewart, Nursel Elcioğlu, M. M. Rajadhyaksha, Martine Le Merrer, Gideon Bach, Annick Raas‐Rothschild	2006	50
10	Mucolipidosis II is caused by mutations in GNPTA encoding the α/β GlcNAc-1-phosphotransferase Nature Medicine ·Stephan Tiede, Stephan Storch, Torben Lübke, Bernard Henrissat, Ruth Bargal, Annick Raas‐Rothschild, Thomas Braulke	2005	146
11	The frequency of mucolipidosis type IV in the Ashkenazi Jewish population and the identification of 3 novel MCOLN1 mutations Human Mutation ·Gideon Bach, Michael B. Webb, Ruth Bargal, Marcia Zeigler, Alexis Garcia-Irons	2005	27
12	Mucolipidosis III type C: first‐trimester biochemical and molecular prenatal diagnosis Prenatal Diagnosis ·Tzipora C. Falik‐Zaccai, M. Zeigler, Ruth Bargal, Gideon Bach, F. K. Talabi, Annick Raas‐Rothschild	2003	6
13	Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C Genetics in Medicine ·Vardiella Meiner, Shoshi Shpitzen, Hanna Mandel, Aharon Klar, Ziva Ben‐Neriah, Joël Zlotogora, Michal Sagi, GENG Xuejiao, Ruth Bargal, Indu Nambiar, Rivka Carmi, Eran Leitersdorf, Marsha Zeigler	2001	28
14	Mucolipidosis type IV: NovelMCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population Human Mutation ·Ruth Bargal, Nili Avidan, Luis Davila-Gomez, Nair Hosino, Marcia Zeigler, Annick Raas‐Rothschild, Ayala Frumkin, Dmitriy Yurievich Pak, Prachi S. Dhokane, Doron Lancet, Gideon Bach	2001	64
15	Identification of the gene causing mucolipidosis type IV Nature Genetics ·Ruth Bargal, Nili Avidan, Edna Ben‐Asher, Pedritto Ferreira Valente, Marcia Zeigler, Ayala Frumkin, Annick Raas‐Rothschild, Gustavo Glusman, Doron Lancet, Gideon Bach	2000	305
16	Mucolipidosis type IV: the origin of the disease in the Ashkenazi Jewish population European Journal of Human Genetics ·Annick Raas‐Rothschild, Ruth Bargal, Sergio DellaPergola, Marcia Zeigler, Gideon Bach	1999	16
17	Niemann Pick Disease type A in Israeli Arabs: 677delT, a common novel single mutation. Mutations in brief no. 161. Online. Human Mutation ·Marta C Amaral, M. Zeigler, Ruth Bargal, Elena Schiff, Gideon Bach	1998	8
18	Mucolipidosis type IV: Accumulation of phospholipids and gangliosides in cultured amniotic cells. A tool for prenatal diagnosis Prenatal Diagnosis ·M. Zeigler, Ruth Bargal, Vaishali Suri, 葛晨霞, Gideon Bach	1992	16
19	Phosphatidylcholine storage in mucolipidosis IV Clinica Chimica Acta ·Ruth Bargal, Gideon Bach	1989	19
20	I-cell disease: Deficiency of extracellular hydrolase phosphorylation Biochemical and Biophysical Research Communications ·Gideon Bach, Ruth Bargal, Michael Cantz	1979	63

About Ruth Bargal

Ruth Bargal is a scholar working on Physiology, Physiology, Cell Biology, Pathology and Forensic Medicine and Rheumatology, having authored 29 papers that have together received 1.2k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (15 papers), Calcium signaling and nucleotide metabolism (14 papers), Cellular transport and secretion (7 papers), Pancreatic function and diabetes (4 papers), Adenosine and Purinergic Signaling (3 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Porphyrin Metabolism and Disorders (2 papers) and Neonatal Health and Biochemistry (2 papers). The work is most often cited by research in Physiology (599 citations), Sensory Systems (252 citations), Cell Biology (392 citations), Physiology (448 citations) and Pharmacology (96 citations). Ruth Bargal has collaborated with scholars based in Israel, United States and France. Frequent co-authors include Gideon Bach, Annick Raas‐Rothschild, Marcia Zeigler, Nili Avidan, Ayala Frumkin, Gustavo Glusman, Doron Lancet, Edna Ben‐Asher, Stephan Tiede and Bernard Henrissat. Their work appears in journals such as Human Mutation, Journal of Inherited Metabolic Disease, Prenatal Diagnosis, Journal of the American Academy of Dermatology and Nature Medicine.

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