Efraim H. Rosenberg

2.5k citations

27 papers · 1.1k indexed · h-index 15

Co-authors: Gajja S. Salomons Cornelis Jakobs Lígia S. Almeida Jan H.M. Schellens Jos H. Beijnen Gabe S. Sonke Serena Marchetti Erik van Werkhoven
Topics: Metabolism and Genetic Disorders (10 papers)Muscle metabolism and nutrition (9 papers)Cancer Genomics and Diagnostics (5 papers)
Cited by: Clinical Biochemistry Cell Biology Cancer Research
Journals: Journal of Clinical Oncology PLoS ONE Annals of Neurology
Partner nations: Netherlands United States Portugal

In The Last Decade

Efraim H. Rosenberg

27 papers receiving 1.1k citations

Peers

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

#	Work	Indexed citations
1	RAD51 recruitment but not replication fork stability associates with PARP inhibitor response in ovarian cancer patient-derived xenograft models 2024 ·NAR Cancer ·Francien Talens,(unknown),Yannick P. Kok,Mengting Chen,Efraim H. Rosenberg,(unknown),Evelien W. Duiker,Nathalie van den Tempel,Markéta Janatová,Petra Zemánková,Petra M. Nederlof,G. Bea A. Wisman,Zdeněk Kleibl,Steven de Jong,Marcel A.T.M. van Vugt	1
2	Impact of genetic counseling strategy on diagnostic yield and workload for genome-sequencing-based tumor diagnostics 2023 ·Genetics in Medicine ·Roelof Koster,Luuk J. Schipper,(unknown),Daphne M. van Beek,(unknown),Kris G. Samsom,Efraim H. Rosenberg,Frans B.L. Hogervorst,Paul Roepman,Mirjam C. Boelens,Linda J.W. Bosch,José G. van den Berg,Gerrit A. Meijer,Emile E. Voest,Edwin Cuppen,Mariëlle Ruijs,Tom van Wezel,Lizet van der Kolk,Kim Monkhorst	2
3	Molecular characterization of gastric adenocarcinoma diagnosed in patients previously treated for Hodgkin lymphoma or testicular cancer 2022 ·PLoS ONE ·(unknown),Pétur Snæbjörnsson,Efraim H. Rosenberg,(unknown),Nicole C.T. van Grieken,Berthe M.P. Aleman,J. Martijn Kerst,Lindsay M. Morton,Michael Schaapveld,Gerrit A. Meijer,Flora E. van Leeuwen,Monique E. van Leerdam,(unknown)	1
4	Challenges in breast cancer genetic testing. A call for novel forms of multidisciplinary care and long-term evaluation 2022 ·Critical Reviews in Oncology/Hematology ·Fred H. Menko,Kim Monkhorst,Frans B.L. Hogervorst,Efraim H. Rosenberg,Muriel A. Adank,Mariëlle Ruijs,Eveline M. A. Bleiker,Gabe S. Sonke,Nicola S. Russell,Hester S. A. Oldenburg,Lizet E. van der Kolk	6
5	[BRCAmutations more frequent in people of Jewish ancestry]. 2019 ·PubMed ·Fred H. Menko,Efraim H. Rosenberg,Lizet E. van der Kolk	1
6	A squamous cell carcinoma in a young woman with Lynch syndrome 2018 ·Familial Cancer ·(unknown),Marianne B. Crijns,Evelien Dekker,Barbara A.J. Bastiaansen,Oren Lapid,Pétur Snæbjörnsson,Efraim H. Rosenberg,Monique E. van Leerdam,Marcel W. Bekkenk	5
7	Crizotinib treatment for patients with EGFR mutation positive NSCLC that acquire cMET amplification after EGFR TKI therapy results in short-lived and heterogeneous responses 2018 ·Lung Cancer ·(unknown),Adrianus J. de Langen,Sayed M.S. Hashemi,Kim Monkhorst,Efraim H. Rosenberg,Daniëlle A.M. Heideman,Teodora Radonic,Egbert F. Smit	15
8	Double somatic mutations in mismatch repair genes are frequent in colorectal cancer after Hodgkin's lymphoma treatment 2016 ·Gut ·(unknown),Pétur Snæbjörnsson,Efraim H. Rosenberg,Peggy N. Atmodimedjo,Berthe M.P. Aleman,Jelle ten Hoeve,Willemina R.R. Geurts-Giele,(unknown),(unknown),(unknown),Gerrit A. Meijer,Hein te Riele,Flora E. van Leeuwen,Winand N.M. Dinjens,Monique E. van Leerdam	27
9	HPV-negative squamous cell carcinoma of the anal canal is unresponsive to standard treatment and frequently carries disruptive mutations in TP53 2015 ·British Journal of Cancer ·Didier Meulendijks,(unknown),L. Dewit,Paul H.M. Smits,(unknown),Marie‐Louise F. van Velthuysen,Efraim H. Rosenberg,Jos H. Beijnen,Jan H.M. Schellens,Annemieke Cats	77
10	Detection of variants in SLC6A8 and functional analysis of unclassified missense variants 2012 ·Molecular Genetics and Metabolism ·(unknown),Ana Pop,Efraim H. Rosenberg,(unknown),Cornelis Jakobs,Gajja S. Salomons	26
11	Characterization of novel SLC6A8 variants with the use of splice-site analysis tools and implementation of a newly developed LOVD database 2010 ·European Journal of Human Genetics ·(unknown),Efraim H. Rosenberg,Lígia S. Almeida,Tjitske Kleefstra,Charles E. Schwartz,Vassili Valayannopoulos,Omar Abdul‐Rahman,Nicola Poplawski,Laura Vilarinho,Philipp Wolf,Johan T. den Dunnen,Cornelis Jakobs,Gajja S. Salomons	15
12	Mutation detection in DNA isolated from cerebrospinal fluid and urine: Clinical utility and pitfalls of multiple displacement amplification 2009 ·Molecular Genetics and Metabolism ·Efraim H. Rosenberg,Eduard A. Struys,Keith Hyland,Barbara Plecko,Paula J. Waters,Saadet Mercimek‐Mahmutoglu,Sylvia Stöckler‐Ipsiroglu,Renata C. Gallagher,Gunter Scharer,Johan L.K. Van Hove,Cornelis Jakobs,Gajja S. Salomons	1
13	Folinic acid–responsive seizures are identical to pyridoxine‐dependent epilepsy 2009 ·Annals of Neurology ·Renata C. Gallagher,Johan L.K. Van Hove,Gunter Scharer,Keith Hyland,Barbara Plecko,Paula J. Waters,(unknown),Sylvia Stöckler‐Ipsiroglu,Gajja S. Salomons,Efraim H. Rosenberg,Eduard A. Struys,Cornelis Jakobs	117
14	Detection of low-level somatic and germline mosaicism by denaturing high-performance liquid chromatography in a EURO-MRX family with SLC6A8 deficiency 2008 ·Neurogenetics ·(unknown),Jiddeke M. van de Kamp,(unknown),Efraim H. Rosenberg,Arjan P.M. de Brouwer,Petra J. W. Pouwels,Marjo S. van der Knaap,Grazia M.S. Mancini,Cornelis Jakobs,Ben C.J. Hamel,Gajja S. Salomons	25
15	A prevalent pathogenic GAMT mutation (c.59G>C) in Portugal 2007 ·Molecular Genetics and Metabolism ·Lígia S. Almeida,Laura Vilarinho,(unknown),Efraim H. Rosenberg,(unknown),C. Jakobs,Gajja S. Salomons	17
16	Functional characterization of missense variants in the creatine transporter gene (SLC6A8): improved diagnostic application 2007 ·Human Mutation ·Efraim H. Rosenberg,(unknown),(unknown),Silvy J.M. van Dooren,(unknown),Cornelis Jakobs,Ton J. deGrauw,Tjitske Kleefstra,Charles E. Schwartz,Gajja S. Salomons	49
17	Overexpression of GAMT restores GAMT activity in primary GAMT-deficient fibroblasts 2006 ·Molecular Genetics and Metabolism ·Lígia S. Almeida,Efraim H. Rosenberg,(unknown),Nanda M. Verhoeven,Laura Vilarinho,C. Jakobs,Gajja S. Salomons	6
18	X-linked creatine transporter (SLC6A8) mutations in about 1% of males with mental retardation of unknown etiology 2006 ·Human Genetics ·Amy J. Clark,Efraim H. Rosenberg,Lígia S. Almeida,Tim Wood,Cornelis Jakobs,Roger E. Stevenson,Charles E. Schwartz,Gajja S. Salomons	101
19	High Prevalence of SLC6A8 Deficiency in X-Linked Mental Retardation 2004 ·The American Journal of Human Genetics ·Efraim H. Rosenberg,Lígia S. Almeida,Tjitske Kleefstra,(unknown),Helger G. Yntema,Nadia Bahi,Claude Moraine,Hans‐Hilger Ropers,Jean‐Pierre Fryns,Ton J. deGrauw,Cornelis Jakobs,Gajja S. Salomons	148
20	Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene 2001 ·Genes Chromosomes and Cancer ·Peter E.M. Taschner,Jeroen C. Jansen,Bora E. Baysal,Anne Marie Bosch,Efraim H. Rosenberg,Annette Bröcker‐Vriends,Andel G. L. van der Mey,Gert‐Jan B. van Ommen,Cees J. Cornelisse,Peter Devilee	133

About Efraim H. Rosenberg

Efraim H. Rosenberg is a scholar working on Clinical Biochemistry, Cell Biology and Cancer Research, having authored 27 papers that have together received 1.1k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (10 papers), Muscle metabolism and nutrition (9 papers) and Cancer Genomics and Diagnostics (5 papers). The work is most often cited by research in Clinical Biochemistry (316 citations), Cell Biology (320 citations) and Cancer Research (163 citations). Efraim H. Rosenberg has collaborated with scholars based in Netherlands, United States and Portugal. Frequent co-authors include Gajja S. Salomons, Cornelis Jakobs, Lígia S. Almeida, Jan H.M. Schellens, Jos H. Beijnen, Gabe S. Sonke, Serena Marchetti, Erik van Werkhoven, Charles E. Schwartz and Robin M.J.M. van Geel. Their work appears in journals such as Journal of Clinical Oncology, PLoS ONE and Annals of Neurology.

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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