Ruth Sheffer

1.2k total citations
22 papers, 627 citations indexed

About

Ruth Sheffer is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ruth Sheffer has authored 22 papers receiving a total of 627 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ruth Sheffer's work include Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (3 papers) and ATP Synthase and ATPases Research (3 papers). Ruth Sheffer is often cited by papers focused on Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (3 papers) and ATP Synthase and ATPases Research (3 papers). Ruth Sheffer collaborates with scholars based in Israel, United States and France. Ruth Sheffer's co-authors include Sterling K. Clarren, Christopher F. Hoth, Aubrey Milunsky, Clinton T. Baldwin, Vardiella Meiner, Liza Douiev, Ann Saada, Joël Zlotogora, Simon Edvardson and Devorah Soiferman and has published in prestigious journals such as Journal of Biological Chemistry, Neurology and Scientific Reports.

In The Last Decade

Ruth Sheffer

21 papers receiving 620 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ruth Sheffer Israel	14	417	156	118	94	61	22	627
Morad Khayat Israel	16	422 1.0×	162 1.0×	73 0.6×	115 1.2×	46 0.8×	50	664
Imen Dorboz France	14	492 1.2×	94 0.6×	67 0.6×	50 0.5×	59 1.0×	30	650
Cécile Rouzier France	16	618 1.5×	152 1.0×	200 1.7×	206 2.2×	94 1.5×	42	842
Hanna Mierzewska Poland	15	444 1.1×	127 0.8×	55 0.5×	126 1.3×	105 1.7×	57	728
Rosarelis Torres United States	12	439 1.1×	168 1.1×	268 2.3×	21 0.2×	57 0.9×	16	733
J. Bronwyn Bateman United States	16	460 1.1×	257 1.6×	78 0.7×	18 0.2×	44 0.7×	34	680
Katharina Steindl Switzerland	18	411 1.0×	323 2.1×	52 0.4×	38 0.4×	49 0.8×	50	698
Aurélien Trimouille France	12	237 0.6×	121 0.8×	143 1.2×	16 0.2×	32 0.5×	25	427
Josef Ekstein United States	12	407 1.0×	193 1.2×	122 1.0×	27 0.3×	170 2.8×	27	851
Lisa McKie United Kingdom	13	433 1.0×	128 0.8×	218 1.8×	8 0.1×	67 1.1×	24	702

Countries citing papers authored by Ruth Sheffer

Since Specialization

Citations

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

Fields of papers citing papers by Ruth Sheffer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruth Sheffer

This figure shows the co-authorship network connecting the top 25 collaborators of Ruth Sheffer. A scholar is included among the top collaborators of Ruth Sheffer based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ruth Sheffer. Ruth Sheffer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Khateb, Samer, Ruth Sheffer, Tamar Ben‐Yosef, et al.. (2022). Relatively mild blue cone monochromacy phenotype caused by various haplotypes in the L- and M-cone opsin genes.. PubMed. 28. 21–28. 1 indexed citations

Yigit, Gökhan, Ruth Sheffer, Yun Li, et al.. (2021). Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state. Journal of Medical Genetics. 59(6). 549–553. 10 indexed citations

Douiev, Liza, Ruth Sheffer, Gabriella Horváth, & Ann Saada. (2020). Bezafibrate Improves Mitochondrial Fission and Function in DNM1L-Deficient Patient Cells. Cells. 9(2). 301–301. 24 indexed citations

Sheffer, Ruth, Michal Gur, Rebecca Brooks, et al.. (2019). Biallelic variants in AGTPBP1, involved in tubulin deglutamylation, are associated with cerebellar degeneration and motor neuropathy. European Journal of Human Genetics. 27(9). 1419–1426. 29 indexed citations

Zelinger, Lina, Christina Zeitz, Karen Hendler, et al.. (2019). TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations. Scientific Reports. 9(1). 12047–12047. 15 indexed citations

Sheffer, Ruth, et al.. (2018). Mechanistic insights into the cellular effects of a novel FN1 variant associated with a spondylometaphyseal dysplasia. Clinical Genetics. 94(5). 429–437. 14 indexed citations

Garza-López, Edgar, et al.. (2018). Role of a conserved glutamine in the function of voltage-gated Ca2+ channels revealed by a mutation in human CACNA1D. Journal of Biological Chemistry. 293(37). 14444–14454. 13 indexed citations

Sheffer, Ruth, et al.. (2016). Quantitative measurement of urinary glycosaminoglycans using a modified DMB method facilitates the diagnosis and monitoring of mucopolysaccharidoses. 2(3). 163–167.

Sheffer, Ruth, Liza Douiev, Simon Edvardson, et al.. (2016). Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function. American Journal of Medical Genetics Part A. 170(6). 1603–1607. 78 indexed citations

10.

Sheffer, Ruth, Yaacov Barak, Simon Edvardson, et al.. (2014). Hindbrain malformation and myoclonic seizures associated with a deleterious mutation in the INPP4A gene. Neurogenetics. 16(1). 23–26. 10 indexed citations

11.

Ramot, Yuval, Koji Sayama, Ruth Sheffer, et al.. (2010). Early-onset sensorineural hearing loss is a prominent feature of H syndrome. International Journal of Pediatric Otorhinolaryngology. 74(7). 825–827. 15 indexed citations

12.

Ashoor, Ghalia, et al.. (2006). A novel mutation in the 12(R)-lipoxygenase (ALOX12B) gene underlies nonbullous congenital ichthyosiform erythroderma. British Journal of Dermatology. 155(1). 198–200. 7 indexed citations

13.

Cai, Juanliang, Barbara K. Goodman, Ankita Patel, et al.. (2003). Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screening. Human Genetics. 114(1). 68–76. 54 indexed citations

14.

Patlas, Michael N., Moran Shapira, A Nagler, Ruth Sheffer, & John M. Gomori. (2001). MRI of mannosidosis. Neuroradiology. 43(11). 941–943. 17 indexed citations

15.

Shohat, Mordechai, Bella Davidov, Gad Barkai, et al.. (1995). Amniocentesis rate and the detection of down syndrome and other chromosomal anomalies in Israel. Prenatal Diagnosis. 15(10). 967–970. 12 indexed citations

16.

Sheffer, Ruth, et al.. (1993). Mucolipidosis type IV: A mild form with late onset. American Journal of Medical Genetics. 47(3). 392–394. 24 indexed citations

17.

Hoth, Christopher F., et al.. (1993). Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I).. PubMed. 52(3). 455–62. 191 indexed citations

18.

Sheffer, Ruth & Joël Zlotogora. (1992). Autosomal dominant inheritance of Klein–Waardenburg syndrome. American Journal of Medical Genetics. 42(3). 320–322. 24 indexed citations

19.

Sheffer, Ruth, et al.. (1992). Behr's Syndrome and 3-Methylglutaconic Aciduria. American Journal of Ophthalmology. 114(4). 494–497. 16 indexed citations

20.

Sheffer, Ruth, et al.. (1988). Disturbed patterns of globin chain synthesis in childhood monosomy 7 myeloproliferative syndrome. British Journal of Haematology. 68(3). 357–362. 5 indexed citations

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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