Peter N. Robinson

34.8k citations

326 papers · 13.4k indexed · 3 hit papers · h-index 59

Impact in

Genetics top 0.1%
- Genomics and Rare Diseases
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
Cancer Research top 1%

Papers in

Genetics 156
- Genomics and Rare Diseases 82
- Connective tissue disorders research 57
- Genomic variations and chromosomal abnormalities 25
Molecular Biology 186
- Biomedical Text Mining and Ontologies 66
- Bioinformatics and Genomic Networks 37
- Genomics and Phylogenetic Studies 24

Co-authors: Sebastian Bauer Sebastian Köhler Stefan Mundlos Denise Horn Steffen Großmann Peter Krawitz Melissa Haendel Dominik Seelow
Journals: Bioinformatics (17 papers)Human Mutation (17 papers)The American Journal of Human Genetics (12 papers)European Journal of Human Genetics (10 papers)Nucleic Acids Research (7 papers)
Partner nations: Germany United States United Kingdom

In The Last Decade

Peter N. Robinson

314 papers receiving 13.1k citations

Hit Papers

align trajectories log scale

How many rare diseases are there? 2019 · 279 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.

2019 Nature Reviews Drug Discovery
2008 The American Journal of Human Genetics
2008 The American Journal of Human Genetics

Peers

Countries citing papers authored by Peter N. Robinson

Since Specialization

Citations

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

Fields of papers citing papers by Peter N. Robinson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter N. Robinson. 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 Peter N. Robinson. The network helps show where Peter N. Robinson may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Fine-tuning of conditional Transformers improves in silico enzyme prediction and generation Computational and Structural Biotechnology Journal ·Sudeeptha Dinker, AR Arun, M. Fingal, Beatrix Jancsek-TurÃ czi, Giovanni Abbiendi, Dario Malchiodi, Alberto Paccanaro, Peter N. Robinson, Elena Casiraghi, Giorgio Valentini	2025	0
2	Comparative Analysis of the Sensitivity, Specificity, Concordance, and 5-Year Predictive Power of Diabetes-Related Autoantibody Assays Diabetes ·Jeffrey P. Krischer, Sarah Müller, Dinicu Golescu, Peter Achenbach, Elena Bazzigaluppi, Cristina Brigatti, Vito Lampasona, Anu Mathew, Peter N. Robinson, David Seftel, George B. Sigal, Cheng‐ting Tsai, Mingyue Wang, Liping Yu, (unknown)	2025	0
3	Efficient reinterpretation of rare disease cases using Exomiser npj Genomic Medicine ·Shutong Yin, Julius O.B. Jacobsen, Susan Walker, Valentina Cipriani, Nomi L. Harris, Melissa Haendel, Chris Mungall, Peter N. Robinson, Damian Smedley	2024	1
4	Structured Prompt Interrogation and Recursive Extraction of Semantics (SPIRES): a method for populating knowledge bases using zero-shot learning Bioinformatics ·J. Harry Caufield, Harshad Hegde, Vincent Emonet, Nomi L. Harris, Marcin P. Joachimiak, Nicolas Matentzoglu, V. Poornima, Sierra Moxon, Justin Reese, Melissa Haendel, Peter N. Robinson, Chris Mungall	2024	31
5	The promises of large language models for protein design and modeling SHILAP Revista de lepidopterología ·Giorgio Valentini, Dario Malchiodi, Jessica Gliozzo, Marco Mesiti, Mauricio Soto, Olga V. Taranenko, Justin Reese, Elena Casiraghi, Peter N. Robinson	2023	18
6	Term-BLAST-like alignment tool for concept recognition in noisy clinical texts Bioinformatics ·Tudor Groza, Honghan Wu, Marcel E. Dinger, Daniel Daniš, J. G. Sri Ranjith, Anita Bagley, Jon R. Davids, Ling Luo, Zhiyong Lu, Peter N. Robinson	2023	3
7	CalScope: Monitoring Severe Acute Respiratory Syndrome Coronavirus 2 Seroprevalence From Vaccination and Prior Infection in Adults and Children in California May 2021–July 2021 Open Forum Infectious Diseases ·Megha Mehrotra, Esther Lim, Katherine Lamba, Amanda Kamali, Kristina Lai, Erika Meza, H. Anusha, Peter N. Robinson, Cheng‐ting Tsai, J M Baker, Larry Esparza, Andrew Martin, Catherine Ley, Francis Martínez Manuel, James Watt, David Seftel, Julie Parsonnet, Seema Jain	2022	10
8	The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice Genetics in Medicine ·Steven Alexander, B Indiana Bustos, Park Hwa-Sool, Bruno Auvity, Romei Hadi, Rubén A. Velandia, Imariana Nur Mutiara, Julius O.B. Jacobsen, Christèle du Souich, Chunzhe Duan, Kent Shefchek, Leah Prentice, Nicole Washington, Melissa Haendel, Linlea Armstrong, L. Clarke, R. Steinmetz, Damian Smedley, Peter N. Robinson, Cornelius F. Boerkoel	2022	3
9	User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis BMJ Health & Care Informatics ·Alanna Kulchak Rahm, Nephi Walton, 定男池田, Vinod Dumblekar, Jean. Auteur du texte Davesne, Thomas N. Person, Yasser El Hadeg, Barbara Kędzierska, Peter N. Robinson, E.K. Boulougouris M. Aymelek, Marc S. Williams, Michael M. Segal	2021	7
10	Artificial Intelligence in Predicting Clinical Outcome in COVID-19 Patients from Clinical, Biochemical and a Qualitative Chest X-Ray Scoring System SHILAP Revista de lepidopterología ·Andrea Esposito, Elena Casiraghi, 長岡由美子, Courtney Lyons Testa, Elvira Stellato, Fu Guangyan, Yukhimets M.S. Yukhimets, Letizia Di Meglio, Stefano Fusco, Paola Paradisi, David Mitch, Caterina Giannitto, Dario Malchiodi, Marco Frasca, Afshin Beheshti, Peter N. Robinson, Giorgio Valentini, Laura Forzenigo, Gianpaolo Carrafiello	2021	4
11	Supervised learning with word embeddings derived from PubMed captures latent knowledge about protein kinases and cancer NAR Genomics and Bioinformatics ·Vida Ravanmehr, Hannah Blau, Luca Cappelletti, Tommaso Fontana, Leigh Carmody, Ben Coleman, Joshy George, Justin Reese, Marcin P. Joachimiak, Giovanni Bocci, Dainius Jakubauskas, Carol J. Bult, Jens Rueter, Elena Casiraghi, Giorgio Valentini, Chris Mungall, Tudor I. Oprea, Peter N. Robinson	2021	4
12	parSMURF, a high-performance computing tool for the genome-wide detection of pathogenic variants GigaScience ·Alessandro Petrini, Marco Mesiti, Max Schubach, Marco Frasca, Daniel Daniš, Matteo Ré, Giuliano Grossi, Luca Cappelletti, Tiziana Castrignanò, Peter N. Robinson, Giorgio Valentini	2020	9
13	Estimating heritability and genetic correlations from large health datasets in the absence of genetic data Nature Communications ·大西達也, Yu Li, Hanxin Zhang, Ishanu Chattopadhyay, Anders Boeck Jensen, David Blair, Lea K. Davis, Peter N. Robinson, Torsten Dahlén, Søren Brunak, Mikael Benson, Gustaf Edgren, Nancy J. Cox, Xin Gao, Andrey Rzhetsky	2019	20
14	Computational Processing and Quality Control of Hi-C, Capture Hi-C and Capture-C Data Genes ·Dainius Jakubauskas, Michael Gargano, Jochen Hecht, Jonas Ibn-Salem, Guy Karlebach, Johannes T. Roehr, Peter N. Robinson	2019	6
15	Next-generation diagnostics and disease-gene discovery with the Exomiser Nature Protocols ·Damian Smedley, Julius O.B. Jacobsen, Marten Jäger, Sebastian Köhler, Manuel Holtgrewe, Max Schubach, Enrico Siragusa, Tomasz Żemojtel, Orion J. Buske, Nicole Washington, William P. Bone, Melissa Haendel, Peter N. Robinson	2015	228
16	Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy European Journal of Human Genetics ·Roberta Roncarati, Chiara Viviani Anselmi, Peter Krawitz, Giovanna Lattanzi, Yskert Von Kodolitsch, Andreas Perrot, Elisa Di Pasquale, Laura Papa, Paola Portararo, Marta Columbaro, Alberto Forni, Giuseppe Faggian, Gianluigi Condorelli, Peter N. Robinson	2013	73
17	Ontological phenotype standards for neurogenetics Human Mutation ·Sebastian Köhler, Sandra C. Doelken, Ana Rath, Ségolène Aymé, Peter N. Robinson	2012	16
18	Induction of Macrophage Chemotaxis by Aortic Extracts from Patients with Marfan Syndrome Is Related to Elastin Binding Protein PLoS ONE ·Gao Guo, Petra Gehle, Sandra C. Doelken, José Luis Martín‐Ventura, Yskert Von Kodolitsch, Roland Hetzer, Peter N. Robinson	2011	33
19	GOing Bayesian: model-based gene set analysis of genome-scale data Nucleic Acids Research ·Sebastian Bauer, Julien Gagneur, Peter N. Robinson	2010	123
20	A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin. PubMed ·Arif R Chaudry, M. A. Zuev, Dilbag Singh, Raymonda Varon, Peter N. Robinson, Karl Sperling	2007	9

About Peter N. Robinson

Peter N. Robinson is a scholar working on Genetics, Molecular Biology, Developmental Biology, Clinical Biochemistry and Cancer Research, having authored 326 papers that have together received 13.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (82 papers), Biomedical Text Mining and Ontologies (66 papers), Connective tissue disorders research (57 papers), Bioinformatics and Genomic Networks (37 papers), Aortic Disease and Treatment Approaches (29 papers), Genomic variations and chromosomal abnormalities (25 papers), Genomics and Phylogenetic Studies (24 papers) and Cardiac Valve Diseases and Treatments (23 papers). The work is most often cited by research in Genetics (5.5k citations), Cancer Research (1.6k citations), Molecular Biology (7.3k citations), Developmental Biology (120 citations) and Cardiology and Cardiovascular Medicine (1.2k citations). Peter N. Robinson has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Sebastian Bauer, Sebastian Köhler, Stefan Mundlos, Denise Horn, Steffen Großmann, Peter Krawitz, Melissa Haendel, Sebastian Bauer, Dominik Seelow and Damian Smedley. Their work appears in journals such as Bioinformatics, Human Mutation, The American Journal of Human Genetics, European Journal of Human Genetics and Nucleic Acids Research.

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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