Efraim H. Rosenberg

2.5k total citations
27 papers, 1.1k citations indexed

About

Efraim H. Rosenberg is a scholar working on Clinical Biochemistry, Cell Biology and Oncology. According to data from OpenAlex, Efraim H. Rosenberg has authored 27 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Clinical Biochemistry, 9 papers in Cell Biology and 8 papers in Oncology. Recurrent topics in Efraim H. Rosenberg's work include Metabolism and Genetic Disorders (10 papers), Muscle metabolism and nutrition (9 papers) and Cancer Genomics and Diagnostics (5 papers). Efraim H. Rosenberg is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Muscle metabolism and nutrition (9 papers) and Cancer Genomics and Diagnostics (5 papers). Efraim H. Rosenberg collaborates with scholars based in Netherlands, United States and Portugal. Efraim H. Rosenberg's co-authors include Gajja S. Salomons, Cornelis Jakobs, Lígia S. Almeida, Jan H.M. Schellens, Jos H. Beijnen, Gabe S. Sonke, Erik van Werkhoven, Dick Pluim, Suzanne Leijen and Robin M.J.M. van Geel and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Annals of Neurology.

In The Last Decade

Efraim H. Rosenberg

27 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Efraim H. Rosenberg Netherlands	15	413	320	316	235	214	27	1.1k
V. Poulaki United States	17	735 1.8×	64 0.2×	121 0.4×	300 1.3×	60 0.3×	34	1.3k
Rosa Aledo Spain	20	507 1.2×	66 0.2×	79 0.3×	58 0.2×	130 0.6×	36	882
Karen Keough United States	10	364 0.9×	64 0.2×	169 0.5×	51 0.2×	52 0.2×	16	878
Shun-Ai Li Japan	14	643 1.6×	188 0.6×	99 0.3×	52 0.2×	59 0.3×	17	1.0k
Vedam L. Ramprasad India	18	534 1.3×	90 0.3×	111 0.4×	51 0.2×	42 0.2×	61	1.1k
Mahnaz Bonrouhi Germany	14	493 1.2×	105 0.3×	30 0.1×	114 0.5×	134 0.6×	21	947
Oleg A. Shchelochkov United States	24	746 1.8×	55 0.2×	460 1.5×	36 0.2×	172 0.8×	47	1.3k
Mohga El‐Abbadi United States	14	439 1.1×	55 0.2×	55 0.2×	69 0.3×	80 0.4×	15	1.1k
Paul McGuire United States	18	580 1.4×	63 0.2×	107 0.3×	79 0.3×	62 0.3×	27	1.6k
Souska Zandi Switzerland	23	440 1.1×	64 0.2×	63 0.2×	138 0.6×	105 0.5×	59	1.4k

Countries citing papers authored by Efraim H. Rosenberg

Since Specialization

Citations

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

Fields of papers citing papers by Efraim H. Rosenberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Efraim H. Rosenberg. 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 Efraim H. Rosenberg. The network helps show where Efraim H. Rosenberg may publish in the future.

Co-authorship network of co-authors of Efraim H. Rosenberg

This figure shows the co-authorship network connecting the top 25 collaborators of Efraim H. Rosenberg. A scholar is included among the top collaborators of Efraim H. Rosenberg 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 Efraim H. Rosenberg. Efraim H. Rosenberg 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

Talens, Francien, Yannick P. Kok, Mengting Chen, et al.. (2024). RAD51 recruitment but not replication fork stability associates with PARP inhibitor response in ovarian cancer patient-derived xenograft models. NAR Cancer. 6(4). zcae044–zcae044. 1 indexed citations

Snæbjörnsson, Pétur, Efraim H. Rosenberg, Nicole C.T. van Grieken, et al.. (2022). Molecular characterization of gastric adenocarcinoma diagnosed in patients previously treated for Hodgkin lymphoma or testicular cancer. PLoS ONE. 17(7). e0270591–e0270591. 1 indexed citations

Menko, Fred H., Kim Monkhorst, Frans B.L. Hogervorst, et al.. (2022). Challenges in breast cancer genetic testing. A call for novel forms of multidisciplinary care and long-term evaluation. Critical Reviews in Oncology/Hematology. 176. 103642–103642. 6 indexed citations

Langen, Adrianus J. de, Sayed M.S. Hashemi, Kim Monkhorst, et al.. (2018). Crizotinib treatment for patients with EGFR mutation positive NSCLC that acquire cMET amplification after EGFR TKI therapy results in short-lived and heterogeneous responses. Lung Cancer. 124. 130–134. 15 indexed citations

Crijns, Marianne B., Evelien Dekker, Barbara A.J. Bastiaansen, et al.. (2018). A squamous cell carcinoma in a young woman with Lynch syndrome. Familial Cancer. 18(2). 193–196. 5 indexed citations

Snæbjörnsson, Pétur, Efraim H. Rosenberg, Peggy N. Atmodimedjo, et al.. (2016). Double somatic mutations in mismatch repair genes are frequent in colorectal cancer after Hodgkin's lymphoma treatment. Gut. 67(3). 447–455. 27 indexed citations

Meulendijks, Didier, L. Dewit, Paul H.M. Smits, et al.. (2015). HPV-negative squamous cell carcinoma of the anal canal is unresponsive to standard treatment and frequently carries disruptive mutations in TP53. British Journal of Cancer. 112(8). 1358–1366. 77 indexed citations

Pop, Ana, et al.. (2012). Detection of variants in SLC6A8 and functional analysis of unclassified missense variants. Molecular Genetics and Metabolism. 105(4). 596–601. 26 indexed citations

Rosenberg, Efraim H., Lígia S. Almeida, Tjitske Kleefstra, et al.. (2010). Characterization of novel SLC6A8 variants with the use of splice-site analysis tools and implementation of a newly developed LOVD database. European Journal of Human Genetics. 19(1). 56–63. 15 indexed citations

10.

Rosenberg, Efraim H., Eduard A. Struys, Keith Hyland, et al.. (2009). Mutation detection in DNA isolated from cerebrospinal fluid and urine: Clinical utility and pitfalls of multiple displacement amplification. Molecular Genetics and Metabolism. 97(4). 312–314. 1 indexed citations

11.

Gallagher, Renata C., Johan L.K. Van Hove, Gunter Scharer, et al.. (2009). Folinic acid–responsive seizures are identical to pyridoxine‐dependent epilepsy. Annals of Neurology. 65(5). 550–556. 117 indexed citations

12.

Kamp, Jiddeke M. van de, Efraim H. Rosenberg, Arjan P.M. de Brouwer, et al.. (2008). Detection of low-level somatic and germline mosaicism by denaturing high-performance liquid chromatography in a EURO-MRX family with SLC6A8 deficiency. Neurogenetics. 9(3). 183–190. 25 indexed citations

13.

Rosenberg, Efraim H., Silvy J.M. van Dooren, Cornelis Jakobs, et al.. (2007). Functional characterization of missense variants in the creatine transporter gene (SLC6A8): improved diagnostic application. Human Mutation. 28(9). 890–896. 49 indexed citations

14.

Almeida, Lígia S., et al.. (2007). A prevalent pathogenic GAMT mutation (c.59G>C) in Portugal. Molecular Genetics and Metabolism. 91(1). 1–6. 17 indexed citations

15.

Clark, Amy J., Efraim H. Rosenberg, Lígia S. Almeida, et al.. (2006). X-linked creatine transporter (SLC6A8) mutations in about 1% of males with mental retardation of unknown etiology. Human Genetics. 119(6). 604–610. 101 indexed citations

16.

Almeida, Lígia S., Efraim H. Rosenberg, Nanda M. Verhoeven, et al.. (2006). Overexpression of GAMT restores GAMT activity in primary GAMT-deficient fibroblasts. Molecular Genetics and Metabolism. 89(4). 392–394. 6 indexed citations

17.

Rosenberg, Efraim H., et al.. (2006). Overexpression of wild‐type creatine transporter (SLC6A8) restores creatine uptake in primary SLC6A8‐deficient fibroblasts. Journal of Inherited Metabolic Disease. 29(2-3). 345–346. 5 indexed citations

18.

Almeida, Lígia S., Efraim H. Rosenberg, Nanda M. Verhoeven, Cornelis Jakobs, & Gajja S. Salomons. (2006). Are cerebral creatine deficiency syndromes on the radar screen?. Future Neurology. 1(5). 637–649. 12 indexed citations

19.

Rosenberg, Efraim H., Lígia S. Almeida, Tjitske Kleefstra, et al.. (2004). High Prevalence of SLC6A8 Deficiency in X-Linked Mental Retardation. The American Journal of Human Genetics. 75(1). 97–105. 148 indexed citations

20.

Taschner, Peter E.M., Jeroen C. Jansen, Bora E. Baysal, et al.. (2001). Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene. Genes Chromosomes and Cancer. 31(3). 274–281. 133 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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