Diana Rajan

11.9k total citations · 1 hit paper
10 papers, 1.8k citations indexed

About

Diana Rajan is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Diana Rajan has authored 10 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 2 papers in Plant Science. Recurrent topics in Diana Rajan's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (3 papers) and RNA modifications and cancer (2 papers). Diana Rajan is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (3 papers) and RNA modifications and cancer (2 papers). Diana Rajan collaborates with scholars based in United Kingdom, Belgium and Netherlands. Diana Rajan's co-authors include Nigel P. Carter, Stephen Clayton, Helen V. Firth, Manuel Corpas, A. Paul Bevan, Steven Van Vooren, Yves Moreau, Shola M. Richards, Matthew E. Hurles and Marcos Miretti and has published in prestigious journals such as Nature Genetics, Bioinformatics and The American Journal of Human Genetics.

In The Last Decade

Diana Rajan

10 papers receiving 1.8k citations

Hit Papers

align trajectories

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.

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

2009 1.2k citations Helen V. Firth, Shola M. Richards et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by Diana Rajan

Since Specialization

Citations

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

Fields of papers citing papers by Diana Rajan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diana Rajan

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Optimization of high-throughput 16S rRNA gene amplicon sequencing: an assessment of PCR pooling, mastermix use and contamination 2023 ·Microbial Genomics ·Dinesh Aggarwal, Diana Rajan, (unknown), Emma Betteridge, (unknown), Catarina Sousa, (unknown), Julian Parkhill, Sharon J. Peacock, Marcus C. de Goffau, Josef Wagner, Ewan M. Harrison	3
2	Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disorders 2021 ·The American Journal of Human Genetics ·Eugene J. Gardner, Alejandro Sifrim, Sarah Lindsay, Elena Prigmore, Diana Rajan, Petr Danecek, Giuseppe Gallone, Ruth Y. Eberhardt, Hilary C. Martin, Caroline F. Wright, David Fitzpatrick, Helen V. Firth, Matthew E. Hurles	11
3	Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders 2018 ·Genetics in Medicine ·Caroline F. Wright, Jeremy F. McRae, Stephen Clayton, Giuseppe Gallone, Stuart Aitken, Tomas Fitzgerald, (unknown), Elena Prigmore, Diana Rajan, Jenny Lord, Alejandro Sifrim, Rosemary E. Kelsell, Michael Parker, Jeffrey C. Barrett, Matthew E. Hurles, David Fitzpatrick, Helen V. Firth	193
4	aCGH.Spline—an R package for aCGH dye bias normalization 2011 ·Bioinformatics ·Tomas Fitzgerald, Lee Larcombe, Solena Le Scouarnec, Stephen Clayton, Diana Rajan, Nigel P. Carter, Richard Redon	4
5	An atypical facial appearance and growth pattern in a child with Cornelia de Lange Syndrome 2011 ·Clinical Dysmorphology ·Jennie Murray, (unknown), Peter M. Gillett, Freddie H. Sharkey, Diana Rajan, Nigel P. Carter, David Fitzpatrick	3
6	FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation 2011 ·Human Molecular Genetics ·George Koumbaris, (unknown), (unknown), Marios Ioannides, Christodoulos Christodoulou, Tomas Fitzgerald, Diana Rajan, Stephen Clayton, Sophia Kitsiou‐Tzeli, Joris Vermeesch, Nicos Skordis, Pavlos Antoniou, Ants Kurg, Ioannis Georgiou, Nigel P. Carter, Philippos C. Patsalis	29
7	Distinct Effects of Allelic NFIX Mutations on Nonsense-Mediated mRNA Decay Engender Either a Sotos-like or a Marshall-Smith Syndrome 2010 ·The American Journal of Human Genetics ·Valérie Malan, Diana Rajan, Sophie Thomas, Adam Shaw, (unknown), Valérie Layet, Marianne Till, Arie van Haeringen, Geert Mortier, Sheela Nampoothiri, Silvija Pušeljić, Laurence Legeai‐Mallet, (unknown), Michel Vekemans, Arnold Münnich, Raoul C. M. Hennekam, Laurence Colleaux, Valérie Cormier‐Daire	107
8	DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources breakdown → 2009 ·The American Journal of Human Genetics ·Helen V. Firth, Shola M. Richards, A. Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, (unknown), Nigel P. Carter	1200
9	Constitutional Haploinsufficiency of Tumor Suppressor Genes in Mentally Retarded Patients With Microdeletions in 17p13.1 2009 ·Cytogenetic and Genome Research ·Ana Cristina Victorino Krepischi, Diana Rajan, I. Karen Temple, (unknown), John A. Crolla, Shuwen Huang, Sarah J. Beal, Paulo Alberto Otto, N. P. Carter, Angela Maria Vianna‐Morgante, Carla Rosenberg	27
10	Germline rates of de novo meiotic deletions and duplications causing several genomic disorders 2007 ·Nature Genetics ·Daniel J. Turner, Marcos Miretti, Diana Rajan, Heike Fiegler, Nigel P. Carter, Martyn Blayney, Stephan Beck, Matthew E. Hurles	225

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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