Michael R. Erdos

39.1k citations

72 papers · 10.0k · 3 hit papers · h-index 45

Impact in

Aging top 0.5%
Molecular Biology top 0.5%
- Nuclear Structure and Function
- RNA Research and Splicing
- Genomics and Chromatin Dynamics
- DNA Repair Mechanisms
- Epigenetics and DNA Methylation
- CRISPR and Genetic Engineering
- Ubiquitin and proteasome pathways

Papers in

Molecular Biology 61
- Nuclear Structure and Function 25
- RNA Research and Splicing 18
- Genomics and Chromatin Dynamics 15
- Epigenetics and DNA Methylation 10
- DNA Repair Mechanisms 9
- Ubiquitin and proteasome pathways 5
Genetics 17
- BRCA gene mutations in cancer 7

Co-authors: Francis S. Collins (49 shared papers)Maria Eriksson (7 shared papers)Leslie B. Gordon (8 shared papers)Kan Cao (8 shared papers)Michael Boehnke (9 shared papers)Laura J. Scott (7 shared papers)Robert D. Goldman (3 shared papers)Anne E. Goldman (3 shared papers)
Journals: Proceedings of the National Academy of Sciences (15 papers)Aging Cell (6 papers)Diabetes (4 papers)Nature (4 papers)Nature Methods (3 papers)
Partner nations: United States United Kingdom Sweden

In The Last Decade

Michael R. Erdos

70 papers receiving 9.8k citations

Michael R. Erdos's Hit Papers

align trajectories log scale

Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging 2006 · 574 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2006 Proceedings of the National Academy of Sciences
2004 Proceedings of the National Academy of Sciences
2003 Nature

Peers

Countries citing papers authored by Michael R. Erdos

Since Specialization

Citations

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

Fields of papers citing papers by Michael R. Erdos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael R. Erdos. 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 Michael R. Erdos. The network helps show where Michael R. Erdos may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 72 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome Nature ·Maria Eriksson, W. Ted Brown, Leslie B. Gordon, Michael W. Glynn, Joel I. Singer, Laura J. Scott, Michael R. Erdos, Christiane M. Robbins, Tracy Moses, Peter Berglund, Amalia Dutra, Evgenia Pak, Sandra G. Durkin, Antonei B. Csòka, Michael Boehnke, Thomas W. Glover, Francis S. Collins Hit paper breakdown →	2003	1633
2	Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson–Gilford progeria syndrome Proceedings of the National Academy of Sciences ·Robert D. Goldman, Dale K. Shumaker, Michael R. Erdos, Maria Eriksson, Anne E. Goldman, Leslie B. Gordon, Yosef Gruenbaum, Satya Khuon, Melissa G. Mendez, Renée Varga, Francis S. Collins Hit paper breakdown →	2004	877
3	Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging Proceedings of the National Academy of Sciences ·Dale K. Shumaker, Thomas Dechat, Alexander Kohlmaier, Stephen A. Adam, Matthew R. Bozovsky, Michael R. Erdos, Maria Eriksson, Anne E. Goldman, Satya Khuon, Francis S. Collins, Thomas Jenuwein, Robert D. Goldman Hit paper breakdown →	2006	574
4	Menin Interacts with the AP1 Transcription Factor JunD and Represses JunD-Activated Transcription Cell ·Sunita Agarwal, Siradanahalli C. Guru, Christina Heppner, Michael R. Erdos, Regina M. Collins, Sylvia Y. Park, Suraj K. Saggar, Settara C. Chandrasekharappa, Francis S. Collins, Allen M. Spiegel, Stephen J. Marx, A. Lee Burns	1999	478
5	BRCA1 Inhibition of Estrogen Receptor Signaling in Transfected Cells Science ·Saijun Fan, J.-A. Wang, Ray‐Hwang Yuan, Yanfen Ma, Qinghui Meng, Michael R. Erdos, Richard G. Pestell, Yuan Fang, Karen J. Auborn, I D Goldberg, E M Rosen	1999	400
6	Cardiovascular Pathology in Hutchinson-Gilford Progeria: Correlation With the Vascular Pathology of Aging Arteriosclerosis Thrombosis and Vascular Biology ·Michelle Olive, Ingrid A. Harten, Richard N. Mitchell, Jeanette Beers, Karima Djabali, Kan Cao, Michael R. Erdos, Cecilia D. Blair, Birgit Funke, Leslie Smoot, Marie Gerhard‐Herman, Jason T. Machan, Robert Kutys, Renu Virmani, Francis S. Collins, Thomas N. Wight, Elizabeth G. Nabel, Leslie B. Gordon	2010	312
7	Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer Nature Genetics ·Lucio H. Castilla, Fergus J. Couch, Michael R. Erdos, Kent Hoskins, (unknown), Judy E. Garber, Jeff Boyd, Matthew Lubin, Michelle L. DeShano, Lawrence C. Brody, Francis S. Collins, Barbara L. Weber	1994	306
8	Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome Proceedings of the National Academy of Sciences ·Brian C. Capell, Michael R. Erdos, James P. Madigan, James J. Fiordalisi, Renée Varga, Karen N. Conneely, Leslie B. Gordon, Channing J. Der, Adrienne D. Cox, Francis S. Collins	2005	306
9	Heterodimerization of the IL-2 receptor β- and γ-chain cytoplasmic domains is required for signalling Nature ·Yoshlaki Nakamura, Sarah M. Russell, Sarah A. Mess, Michael Friedmann, Michael R. Erdos, Christine François, Yannick Jacques, Stephen Adelstein, Warren J. Leonard	1994	282
10	Rapamycin Reverses Cellular Phenotypes and Enhances Mutant Protein Clearance in Hutchinson-Gilford Progeria Syndrome Cells Science Translational Medicine ·Kan Cao, John J. Graziotto, Cecilia D. Blair, Joseph R. Mazzulli, Michael R. Erdos, Dimitri Krainc, Francis S. Collins	2011	280
11	Super-enhancers delineate disease-associated regulatory nodes in T cells Nature ·Golnaz Vahedi, Yuka Kanno, Yasuko Furumoto, Kan Jiang, Stephen C.J. Parker, Michael R. Erdos, Sean Davis, Rahul Roychoudhuri, Nicholas P. Restifo, Massimo Gadina, Zhonghui Tang, Yijun Ruan, Francis S. Collins, Vittorio Sartorelli, John J. O’Shea	2015	277
12	Correlated alterations in genome organization, histone methylation, and DNA–lamin A/C interactions in Hutchinson-Gilford progeria syndrome Genome Research ·Rachel Patton McCord, Ashley Nazario-Toole, Haoyue Zhang, Peter S. Chines, Ye Zhan, Michael R. Erdos, Francis S. Collins, Job Dekker, Kan Cao	2012	242
13	Progerin and telomere dysfunction collaborate to trigger cellular senescence in normal human fibroblasts Journal of Clinical Investigation ·Kan Cao, Cecilia D. Blair, Dina A. Faddah, Julia E. Kieckhaefer, Michelle Olive, Michael R. Erdos, Elizabeth G. Nabel, Francis S. Collins	2011	236
14	Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson–Gilford progeria syndrome Proceedings of the National Academy of Sciences ·Renée Varga, Maria Eriksson, Michael R. Erdos, Michelle Olive, Ingrid A. Harten, Frank D. Kolodgie, Brian C. Capell, Jun Cheng, Dina A. Faddah, Stacie Perkins, Hedwig Avallone, Hong San, Xuan Qu, Santhi K. Ganesh, Leslie B. Gordon, Renu Virmani, Thomas N. Wight, Elizabeth G. Nabel, Francis S. Collins	2006	233
15	Heritable Individual-Specific and Allele-Specific Chromatin Signatures in Humans Science ·Ryan M. McDaniell, Bum-Kyu Lee, Lingyun Song, Zheng Liu, Alan P. Boyle, Michael R. Erdos, Laura J. Scott, Mario A. Morken, Katerina S. Kucera, Anna Battenhouse, Damian Keefe, Francis S. Collins, Huntington F. Willard, Jason D. Lieb, Terrence S. Furey, Gregory E. Crawford, Vishwanath R. Iyer, Ewan Birney	2010	233
16	Role of direct interaction in BRCA1 inhibition of estrogen receptor activity Oncogene ·Saijun Fan, Yong Xian, Chenguang Wang, Ren-qi Yuan, Qinghui Meng, Ji-An Wang, Michael R. Erdos, Itzhak D. Goldberg, Paul Webb, Peter J. Kushner, Richard G. Pestell, Eliot M. Rosen	2001	216
17	A lamin A protein isoform overexpressed in Hutchinson–Gilford progeria syndrome interferes with mitosis in progeria and normal cells Proceedings of the National Academy of Sciences ·Kan Cao, Brian C. Capell, Michael R. Erdos, Karima Djabali, Francis S. Collins	2007	202
18	Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample Diabetes ·Laura J. Scott, Lori L. Bonnycastle, Cristen J. Willer, Andrew G. Sprau, Anne Jackson, Narisu Narisu, William L. Duren, Peter S. Chines, Heather M. Stringham, Michael R. Erdos, Timo T. Valle, Jaakko Tuomilehto, Richard N. Bergman, Karen L. Mohlke, Francis S. Collins, Michael Boehnke	2006	187
19	DNase-chip: a high-resolution method to identify DNase I hypersensitive sites using tiled microarrays Nature Methods ·Gregory E. Crawford, Sean Davis, Peter C. Scacheri, Gabriel Renaud, Mohamad J. Halawi, Michael R. Erdos, Roland Green, Paul S. Meltzer, Tyra G. Wolfsberg, Francis S. Collins	2006	174
20	A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization Proceedings of the National Academy of Sciences ·Pekka Taimen, Katrin Pfleghaar, Takeshi Shimi, Dorothée Möller, Kfir Ben‐Harush, Michael R. Erdos, Stephen A. Adam, Harald Herrmann, Ohad Medalia, Francis S. Collins, Anne E. Goldman, Robert D. Goldman	2009	169

About Michael R. Erdos

Michael R. Erdos is a scholar working on Molecular Biology, Genetics, Oncology, Cell Biology and Surgery, having authored 72 papers that have together received 10.0k indexed citations. Recurring topics across this work include Nuclear Structure and Function (25 papers), RNA Research and Splicing (18 papers), Genomics and Chromatin Dynamics (15 papers), Epigenetics and DNA Methylation (10 papers), DNA Repair Mechanisms (9 papers), Pancreatic function and diabetes (7 papers), BRCA gene mutations in cancer (7 papers) and Ubiquitin and proteasome pathways (5 papers). The work is most often cited by research in Aging (310 citations), Molecular Biology (7.6k citations), Genetics (1.6k citations), Cell Biology (751 citations) and Oncology (1.0k citations). Michael R. Erdos has collaborated with scholars based in United States, United Kingdom and Sweden. Frequent co-authors include Francis S. Collins, Maria Eriksson, Leslie B. Gordon, Kan Cao, Michael Boehnke, Laura J. Scott, Robert D. Goldman, Anne E. Goldman, Satya Khuon and Dale K. Shumaker. Their work appears in journals such as Proceedings of the National Academy of Sciences, Aging Cell, Diabetes, Nature and Nature Methods.

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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Michael R. Erdos

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In The Last Decade

Michael R. Erdos

Michael R. Erdos's Hit Papers

Peers

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Fields of papers citing papers by Michael R. Erdos

All Works

About Michael R. Erdos

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