Nanda R. Rodrigues

4.5k citations

34 papers · 3.8k indexed · 2 hit papers · h-index 20

Genetics top 1%
- Neurogenetic and Muscular Disorders Research 10
- Diabetes and associated disorders 8
Genetics top 2%
- Neurogenetic and Muscular Disorders Research 10
- Diabetes and associated disorders 8
Molecular Biology top 5%
- RNA modifications and cancer 9
- RNA Research and Splicing 6
- Protein Tyrosine Phosphatases 3
- Protein Kinase Regulation and GTPase Signaling 3
- Metabolism, Diabetes, and Cancer 3
Oncology top 5%
Immunology top 5%
Surgery
- Pancreatic function and diabetes 8

Co-authors: R. Duncan Campbell Richard G.H. Cotton Walter F. Bodmer I B Kerr David P. Lane Andrew Rowan Julian Gannon Mark E. Smith
Cited by: Genetics Molecular Biology
Journals: Mammalian Genome (4 papers)Journal of Medical Genetics (3 papers)Proceedings of the National Academy of Sciences (3 papers)
Partner nations: United Kingdom United States Brazil

In The Last Decade

Nanda R. Rodrigues

33 papers receiving 3.8k citations

Hit Papers

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What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

1990 Proceedings of the National Academy of Sciences
1988 Proceedings of the National Academy of Sciences

Peers

Countries citing papers authored by Nanda R. Rodrigues

Since Specialization

Citations

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

Fields of papers citing papers by Nanda R. Rodrigues

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Genetic analysis of autoimmune type 1 diabetes mellitus in mice. 1991. PubMed ·John A. Todd,Timothy J. Aitman,Richard J. Cornall,Soumitra Ghosh,輝宮本,Catherine M. Hearne,Shu-Jie Liang,Jennifer M. Love,Marcia A. McAleer,T. M.,Nanda R. Rodrigues,M Lathrop,A Pressey,Nicole H. DeLarato,Laurence B. Peterson,Linda S. Wicker	2014	0
2	Analysis of mutations in the tudor domain of the survival motor neuron protein SMN European Journal of Human Genetics ·Payam Mohaghegh,Nanda R. Rodrigues,Nicholas Owen,Chris P. Ponting,Thanh T. Le,Arthur H.M. Burghes,Kay E. Davies	1999	25
3	The Mitogen-activated Protein Kinase Phosphatase-3 N-terminal Noncatalytic Region Is Responsible for Tight Substrate Binding and Enzymatic Specificity Journal of Biological Chemistry ·Marco Muda,Aspasia Theodosiou,Corine Gilliéron,Anna L. Smith,Christian Chabert,Montserrat Camps,Ursula Boschert,Nanda R. Rodrigues,Kay E. Davies,Alan Ashworth,Steve Arkinstall	1998	133
4	Missense mutation clustering in the survival motor neuron gene: a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism? Human Molecular Genetics ·Kevin Talbot,Chris P. Ponting,Aspasia Theodosiou,Nanda R. Rodrigues,R. Surtees,R. Mountford,Kay E. Davies	1997	126
5	Update of the Gene Discovery Program in Schistosoma mansoni with the Expressed Sequence Tag Approach Memórias do Instituto Oswaldo Cruz ·Élida Mara Leite Rabelo,Glória Regina Franco,Vasco Azevedo,Marijke Hoflack,Carsten Veller,Amy Peters,Nanda R. Rodrigues,José Miguel Ortega,Sérgio D.J. Pena	1997	4
6	Genomic Organization and Chromosomal Localization of a Member of the MAP Kinase Phosphatase Gene Family to Human Chromosome 11p15.5 and a Pseudogene to 10q11.2 Genomics ·M. Andrew Nesbit,Matt Hodges,Louise J. Campbell,Bethan Moss,Mariëlle Alders,Nanda R. Rodrigues,Kevin Talbot,Aspasia Theodosiou,M. Mannens,Yoshihiko Nakamura,Peter Little,Kay E. Davies	1997	13
7	The Dual Specificity Phosphatases M3/6 and MKP-3 Are Highly Selective for Inactivation of Distinct Mitogen-activated Protein Kinases Journal of Biological Chemistry ·Marco Muda,Aspasia Theodosiou,Nanda R. Rodrigues,Ursula Boschert,Montserrat Camps,Corine Gilliéron,Kay E. Davies,Alan Ashworth,Steve Arkinstall	1996	341
8	Novel transcribed sequences represented in the complex genomic region 5q13 Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·Karen Morrison,Safia Qureshi,Susan M. Anderson,Idrissa Drame,Aspasia Theodosiou,Nanda R. Rodrigues,Derek J. Blake,M. Andrew Nesbit,Kay E. Davies,David J. Porteous,Anthony J. Brookes	1996	7
9	MOLECULAR ANALYSIS OF CHILDHOOD-ONSET SPINAL MUSCULAR-ATROPHY The American Journal of Human Genetics ·Aspasia Theodosiou,Nanda R. Rodrigues,Kevin Talbot,Louise J. Campbell,D Halvorson Ardell,Nicholas Owen,Helen E. Ambrose,F. Muntoni,森川香子,Jaakko Ignatius,Victor Dubowitz,Anandan Sujatha	1995	3
10	Mapping of Retrotransposon Sequences in the Unstable Region Surrounding the Spinal Muscular Atrophy Locus in 5q13 Genomics ·Michael J. Francis,M. Andrew Nesbit,Aspasia Theodosiou,Nanda R. Rodrigues,Louise J. Campbell,Zóe Christodoulou,Safia Qureshi,David J. Porteous,Anthony J. Brookes,K.E. Davies	1995	24
11	Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele. Journal of Medical Genetics ·R.J. Daniels,Louise J. Campbell,Nanda R. Rodrigues,Michael J. Francis,Karen Morrison,Michael D. McLean,Alex MacKenzie,Jaakko Ignatius,Victor Dubowitz,Kay E. Davies	1995	14
12	Mapping of an insulin-dependent diabetes locus, Idd9, in NOD mice to Chromosome 4 Mammalian Genome ·Nanda R. Rodrigues,Richard J. Cornall,Phillip Chandler,Elizabeth Simpson,Linda S. Wicker,Laurence B. Peterson,John A. Todd	1994	36
13	Polygenic control of autoimmune diabetes in nonobese diabetic mice Nature Genetics ·Soumitra Ghosh,Sheila Palmer,Nanda R. Rodrigues,Heather J. Cordell,Catherine M. Hearne,Richard J. Cornall,Jan‐Bas Prins,PE McShane,G.M. Lathrop,L. Peterson,Linda S. Wicker,John A. Todd	1993	251
14	Mouse chromosome 3 Mammalian Genome ·Michael F. Seldin,Jan‐Bas Prins,Nanda R. Rodrigues,John A. Todd,Miriam H. Meisler	1993	11
15	Dissection of the Pathophysiology of Type 1 Diabetes by Genetic Analysis Autoimmunity ·John A. Todd,Peter Reed,Jan‐Bas Prins,Bamy Emely,Sheila Palmer,Heather J. Cordell,Lynn E. Pritchard,Soumitra Ghosh,Richard J. Cornall,Timothy J. Aitman,Nanda R. Rodrigues,Catherine M. Hearne,Marcia A. McAleer,Laurence B. Peterson,Linda S. Wicker	1993	3
16	Mouse Chromosome 3 Mammalian Genome ·Miriam H. Meisler,John A. Todd,Nanda R. Rodrigues,Edward K. Wakeland,Michael F. Seldin	1992	36
17	Linkage analysis of 84 microsatellite markers in intra- and interspecific backcrosses Mammalian Genome ·Marcia A. McAleer,Timothy J. Aitman,Richard J. Cornall,Soumitra Ghosh,Jennifer R. Hall,Catherine M. Hearne,Jennifer M. Love,Jan‐Bas Prins,В. А. Айрапетов,Nanda R. Rodrigues,Nicole H. DeLarato,Laurence B. Peterson,Linda S. Wicker,John A. Todd	1992	16
18	Insulin gene region–encoded susceptibility to type 1 diabetes is not restricted to HLA–DR4–positive individuals Nature Genetics ·Steve Baín,Jan‐Bas Prins,Catherine M. Hearne,Nanda R. Rodrigues,B R Rowe,L E Pritchard,Rachael J. Ritchie,James Hall,Dag E. Undlien,K. S. Rønningen,David B. Dunger,Anthony Barnett,John A. Todd	1992	103
19	Genetic analysis of autoimmune type 1 diabetes mellitus in mice Nature ·John A. Todd,Timothy J. Aitman,Richard J. Cornall,Soumitra Ghosh,Paras C. Maru,Catherine M. Hearne,Andrew M. Knight,Jennifer M. Love,Marcia A. McAleer,Jan‐Bas Prins,Nanda R. Rodrigues,Mark Lathrop,A Pressey,Nicole H. DeLarato,Laurence B. Peterson,Linda S. Wicker	1991	411
20	Further characterization, isolation and identification of the epithelial cell‐surface antigen defined by monoclonal antibody aua1 International Journal of Cancer ·H. Durbin,Nanda R. Rodrigues,Walter F. Bodmer	1990	19

About Nanda R. Rodrigues

Nanda R. Rodrigues is a scholar working on Genetics, Genetics and Molecular Biology, having authored 34 papers that have together received 3.8k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (10 papers), RNA modifications and cancer (9 papers), Diabetes and associated disorders (8 papers), Pancreatic function and diabetes (8 papers), RNA Research and Splicing (6 papers), Protein Tyrosine Phosphatases (3 papers), Protein Kinase Regulation and GTPase Signaling (3 papers) and Metabolism, Diabetes, and Cancer (3 papers). The work is most often cited by research in Genetics (606 citations), Genetics (1.1k citations) and Molecular Biology (2.3k citations). Nanda R. Rodrigues has collaborated with scholars based in United Kingdom, United States and Brazil. Frequent co-authors include R. Duncan Campbell, Richard G.H. Cotton, Walter F. Bodmer, I B Kerr, David P. Lane, Andrew Rowan, Julian Gannon, Mark E. Smith, John A. Todd and Jan‐Bas Prins. Their work appears in journals such as Mammalian Genome, Journal of Medical Genetics, Proceedings of the National Academy of Sciences, Genomics and Nature Genetics.

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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