Paul Renbaum

5.4k total citations
87 papers, 3.2k citations indexed

About

Paul Renbaum is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Paul Renbaum has authored 87 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 34 papers in Pediatrics, Perinatology and Child Health and 34 papers in Genetics. Recurrent topics in Paul Renbaum's work include Prenatal Screening and Diagnostics (22 papers), Genomic variations and chromosomal abnormalities (10 papers) and BRCA gene mutations in cancer (8 papers). Paul Renbaum is often cited by papers focused on Prenatal Screening and Diagnostics (22 papers), Genomic variations and chromosomal abnormalities (10 papers) and BRCA gene mutations in cancer (8 papers). Paul Renbaum collaborates with scholars based in Israel, United States and Palestinian Territory. Paul Renbaum's co-authors include Ephrat Levy‐Lahad, Aharon Razin, Cathy Hammerman, Michael Kaplan, Amnon Lahad, Ernest Beutler, Hadile Ounallah-Saad, Raz Yirmiya, Inbal Goshen and Tirzah Kreisel and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Paul Renbaum

85 papers receiving 3.1k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Paul Renbaum 1.6k 976 816 413 358 87 3.2k
David G. Simmons 1.3k 0.8× 390 0.4× 1.3k 1.6× 334 0.8× 167 0.5× 72 3.3k
Karl Nocka 1.6k 1.0× 436 0.4× 526 0.6× 198 0.5× 93 0.3× 31 3.9k
Leda Dalprà 1.5k 0.9× 1.2k 1.2× 490 0.6× 194 0.5× 491 1.4× 119 3.3k
Carmen Clapp 1.5k 0.9× 412 0.4× 280 0.3× 134 0.3× 414 1.2× 159 4.6k
Heidi Scrable 2.3k 1.4× 516 0.5× 184 0.2× 629 1.5× 511 1.4× 51 4.6k
Paul C. Watkins 2.7k 1.7× 1.5k 1.5× 365 0.4× 194 0.5× 190 0.5× 46 4.9k
Dani Bercovich 1.2k 0.7× 696 0.7× 139 0.2× 213 0.5× 259 0.7× 74 2.9k
Gonzalo Martı́nez de la Escalera 1.3k 0.8× 480 0.5× 209 0.3× 114 0.3× 259 0.7× 152 4.2k
Jean‐Louis Blouin 1.0k 0.7× 1.1k 1.1× 280 0.3× 376 0.9× 205 0.6× 75 2.4k
Hitoshi Osaka 3.0k 1.9× 1.3k 1.4× 317 0.4× 71 0.2× 167 0.5× 235 5.0k

Countries citing papers authored by Paul Renbaum

Since Specialization
Citations

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

Fields of papers citing papers by Paul Renbaum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paul Renbaum

This figure shows the co-authorship network connecting the top 25 collaborators of Paul Renbaum. A scholar is included among the top collaborators of Paul Renbaum 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 Paul Renbaum. Paul Renbaum is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Giacomello, Marta, Chiara Frascarelli, Laurence A. Bindoff, et al.. (2023). PPAR-gamma agonist pioglitazone recovers mitochondrial quality control in fibroblasts from PITRM1-deficient patients. Frontiers in Pharmacology. 14. 1220620–1220620. 5 indexed citations
2.
Backenroth, Daniel, Gheona Altarescu, Omer Murik, et al.. (2023). SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testing. Scientific Reports. 13(1). 18036–18036. 5 indexed citations
3.
Zeevi, David A., Daniel Backenroth, Paul Renbaum, et al.. (2021). Expanded clinical validation of Haploseek for comprehensive preimplantation genetic testing. Genetics in Medicine. 23(7). 1334–1340. 7 indexed citations
4.
Segel, Reeval, Adi Aran, Süleyman Gülsüner, et al.. (2020). A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures. Neurogenetics. 21(4). 259–267. 9 indexed citations
5.
Weinberg‐Shukron, Ariella, Abdulsalam Abu‐Libdeh, Liran Carmel, et al.. (2015). Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress. Journal of Medical Genetics. 52(9). 636–641. 28 indexed citations
6.
Gazy, Inbal, David A. Zeevi, Paul Renbaum, et al.. (2015). TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair. PLoS ONE. 10(7). e0134120–e0134120. 33 indexed citations
7.
Epsztejn‐Litman, Silvina, Gheona Altarescu, Paul Renbaum, et al.. (2015). Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis. PLoS ONE. 10(10). e0138893–e0138893. 4 indexed citations
8.
Duplan, Eric, Jean Sévalle, Julien Viotti, et al.. (2013). Parkin differently regulates presenilin-1 and presenilin-2 functions by direct control of their promoter transcription. Journal of Molecular Cell Biology. 5(2). 132–142. 32 indexed citations
9.
Ben‐Yosef, Dalit, Ami Amit, Mira Malcov, et al.. (2011). Female Sex Bias in Human Embryonic Stem Cell Lines. Stem Cells and Development. 21(3). 363–372. 21 indexed citations
10.
Zangen, David, Yotam Kaufman, Sharon Zeligson, et al.. (2011). XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription. The American Journal of Human Genetics. 89(4). 572–579. 78 indexed citations
11.
Altarescu, Gheona, Paul Renbaum, Rachel Beeri, et al.. (2011). Preimplantation genetic diagnosis (PGD) – prevention of the birth of children affected with endocrine diseases. Journal of Pediatric Endocrinology and Metabolism. 24(7-8). 543–8. 14 indexed citations
12.
Altarescu, Gheona, Paul Renbaum, Talia Eldar‐Geva, et al.. (2011). Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell line. Prenatal Diagnosis. 31(9). 853–860. 12 indexed citations
13.
Reish, Orit, Paul Renbaum, Avi Orr‐Urtreger, et al.. (2010). Frequencies of C282Y and H63D alleles in the HFE gene among various Jewish ethnic groups in Israel: A change of concept required. Genetics in Medicine. 12(2). 122–125. 4 indexed citations
14.
Tsafrir, Avi, Gheona Altarescu, Ehud J. Margalioth, et al.. (2010). PGD for fragile X syndrome: ovarian function is the main determinant of success. Human Reproduction. 25(10). 2629–2636. 23 indexed citations
15.
Altarescu, Gheona, Talia Eldar‐Geva, B. Brooks, et al.. (2009). Real-time reverse linkage using polar body analysis for preimplantation genetic diagnosis in female carriers of de novo mutations. Human Reproduction. 24(12). 3225–3229. 20 indexed citations
16.
Ounallah-Saad, Hadile, Rachel Beeri, Inbal Goshen, et al.. (2009). Transcriptional regulation of the murine Presenilin-2 gene reveals similarities and differences to its human orthologue. Gene. 446(2). 81–89. 8 indexed citations
17.
Kaplan, Michael, Paul Renbaum, Hendrik J. Vreman, et al.. (2007). (TA)n UGT 1A1 Promoter Polymorphism: A Crucial Factor in the Pathophysiology of Jaundice in G-6-PD Deficient Neonates. Pediatric Research. 61(6). 727–731. 27 indexed citations
18.
Kaplan, Michael, Cathy Hammerman, Firmino F. Rubaltelli, et al.. (2002). Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism. Hepatology. 35(4). 905–911. 40 indexed citations
19.
Hornreich, Gila, Uziel Beller, Ofer Lavie, et al.. (1999). Is Uterine Serous Papillary Carcinoma a BRCA1-Related Disease? Case Report and Review of the Literature. Gynecologic Oncology. 75(2). 300–304. 56 indexed citations
20.
Gruenbaum, Yosef, et al.. (1990). Effect of CpG methylation on gene expression in transfected plant protoplasts. Gene. 94(2). 189–193. 18 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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