Jochen Weile

2.5k citations

27 papers · 655 indexed · h-index 12

Impact in

Genetics top 10%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
Molecular Biology
- RNA and protein synthesis mechanisms
- Bioinformatics and Genomic Networks
- CRISPR and Genetic Engineering
- Genomics and Phylogenetic Studies

Papers in ⓘ

Genetics 9
- Genomics and Rare Diseases 8
Molecular Biology 22
- Genomics and Phylogenetic Studies 8
- Bioinformatics and Genomic Networks 5
- CRISPR and Genetic Engineering 4
- Biomedical Text Mining and Ontologies 4
- Ubiquitin and proteasome pathways 3
- Genomics and Chromatin Dynamics 2

Co-authors: Frederick P. Roth (18 shared papers)Douglas M. Fowler (4 shared papers)Alan F. Rubin (2 shared papers)Song Sun (5 shared papers)Yingzhou Wu (3 shared papers)Lea M. Starita (1 shared paper)Jay Shendure (1 shared paper)Anthony T. Papenfuss (1 shared paper)
Journals: Bioinformatics (7 papers)The American Journal of Human Genetics (3 papers)Berichte aus der medizinischen Informatik und Bioinformatik/Journal of integrative bioinformatics (2 papers)Human Mutation (2 papers)Genome biology (2 papers)
Partner nations: Canada United States United Kingdom

In The Last Decade

Jochen Weile

26 papers receiving 650 citations

Peers

Countries citing papers authored by Jochen Weile

Since Specialization

Citations

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

Fields of papers citing papers by Jochen Weile

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jochen Weile, 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 Jochen Weile Line = papers co-authored together Jochen Weile 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 27 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effect Genome biology ·Daniel Esposito, Jochen Weile, Jay Shendure, Lea M. Starita, Anthony T. Papenfuss, Frederick P. Roth, Douglas M. Fowler, Alan F. Rubin	2019	132
2	Multiplexed assays of variant effects contribute to a growing genotype–phenotype atlas Human Genetics ·Jochen Weile, Frederick P. Roth	2018	93
3	Improved pathogenicity prediction for rare human missense variants The American Journal of Human Genetics ·Yingzhou Wu, Hanqing Liu, Roujia Li, Song Sun, Jochen Weile, Frederick P. Roth	2021	79
4	Integrative pathway dissection of molecular mechanisms of moxLDL-induced vascular smooth muscle phenotype transformation BMC Cardiovascular Disorders ·George S. Karagiannis, Jochen Weile, Gary D. Bader, Joe O. Minta	2013	48
5	A proactive genotype-to-patient-phenotype map for cystathionine beta-synthase Genome Medicine ·Song Sun, Jochen Weile, Marta Verby, Yingzhou Wu, Yang Wang, Atina G. Coté, Iosifina Fotiadou, Julia Kitaygorodsky, Marc Vidal, Jasper Rine, Pavel Ješina, Viktor Kožich, Frederick P. Roth	2020	40
6	Systematic analysis of bypass suppression of essential genes Molecular Systems Biology ·Jolanda van Leeuwen, Carles Pons, Guihong Tan, Jason Zi Wang, Jing Hou, Jochen Weile, Marinella Gebbia, Wendy Liang, Ermira Shuteriqi, Zhijian Li, Maykel Lopes, Matej Ušaj, Andreia Dos Santos Lopes, Natascha van Lieshout, Chad L. Myers, Frederick P. Roth, Patrick Aloy, Brenda Andrews, Charles Boone	2020	37
7	KeyPathwayMiner: Detecting Case-Specific Biological Pathways Using Expression Data Internet Mathematics ·Nicolás Alcaraz, Hande Kücük, Jochen Weile, Anil Wipat, Jan Baumbach	2011	34
8	A comprehensive map of human glucokinase variant activity Genome biology ·Sarah Gersing, Matteo Cagiada, Marinella Gebbia, Anette P. Gjesing, Atina G. Coté, Gireesh Seesankar, Roujia Li, Daniel Tabet, Jochen Weile, Amelie Stein, Anna L. Gloyn, Torben Hansen, Frederick P. Roth, Kresten Lindorff‐Larsen, Rasmus Hartmann‐Petersen	2023	28
9	An integrated dataset for in silico drug discovery PubMed ·Simon Cockell, Jochen Weile, Phillip Lord, Claire Wipat, D Andriychenko, Matthew Pocock, Darren J. Wilkinson, Malcolm P. Young, Anil Wipat	2010	24
10	An integrated dataset for in silico drug discovery Berichte aus der medizinischen Informatik und Bioinformatik/Journal of integrative bioinformatics ·Simon Cockell, Jochen Weile, Phillip Lord, Claire Wipat, Dmytro Andriychenko, Matthew Pocock, Darren J. Wilkinson, Malcolm P. Young, Anil Wipat	2010	22
11	MaveRegistry: a collaboration platform for multiplexed assays of variant effect Bioinformatics ·Da Kuang, Jochen Weile, Nishka Kishore, Maria Nguyen, Alan F. Rubin, Stanley Fields, Douglas M. Fowler, Frederick P. Roth	2021	16
12	Genome-scale mapping of DNA damage suppressors through phenotypic CRISPR-Cas9 screens Molecular Cell ·Yichao Zhao, Daniel Tabet, Diana Rubio-Contreras, Linjiang Lao, Arne Nedergaard Kousholt, Jochen Weile, Henrique Melo, Lisa Hoeg, Sumin Feng, Atina G. Coté, Zhen‐Yuan Lin, Dheva Setiaputra, Jos Jonkers, Anne‐Claude Gingras, Fernando Gómez-Herreros, Frederick P. Roth, Daniel Durocher	2023	12
13	CoryneCenter – An online resource for the integrated analysis of corynebacterial genome and transcriptome data BMC Systems Biology ·Heiko Neuweger, Jan Baumbach, Stefan P. Albaum, Thomas Bekel, Michael Dondrup, Andrea T. Hüser, Jörn Kalinowski, Sebastian Oehm, Alfred Pühler, Sven Rahmann, Jochen Weile, Alexander Goesmann	2007	11
14	Assessing predictions of fitness effects of missense mutations in SUMO‐conjugating enzyme UBE2I Human Mutation ·Jing Zhang, Lisa N. Kinch, Qian Cong, Jochen Weile, Song Sun, Atina G. Coté, Frederick P. Roth, Nick V. Grishin	2017	11
15	A web application and service for imputing and visualizing missense variant effect maps Bioinformatics ·Yingzhou Wu, Jochen Weile, Atina G. Coté, Song Sun, Jennifer J. Knapp, Marta Verby, Frederick P. Roth	2019	10
16	Bayesian integration of networks without gold standards Bioinformatics ·Jochen Weile, Katherine James, Jennifer Hallinan, Simon Cockell, Phillip Lord, Anil Wipat, Darren J. Wilkinson	2012	9
17	Prioritizing genes for systematic variant effect mapping Bioinformatics ·Da Kuang, Rebecca Truty, Jochen Weile, Britt Johnson, Keith Nykamp, Carlos L. Araya, Robert L. Nussbaum, Frederick P. Roth	2020	8
18	Assessing predictions on fitness effects of missense variants in calmodulin Human Mutation ·Jing Zhang, Lisa N. Kinch, Qian Cong, Panagiotis Katsonis, Olivier Lichtarge, Castrense Savojardo, Giulia Babbi, Pier Luigi Martelli, Emidio Capriotti, Rita Casadio, Aditi Garg, Debnath Pal, Jochen Weile, Song Sun, Marta Verby, Frederick P. Roth, Nick V. Grishin	2019	7
19	Customizable views on semantically integrated networks for systems biology Bioinformatics ·Jochen Weile, Matthew Pocock, Simon Cockell, Phillip Lord, James M. Dewar, Eva−Maria Holstein, Darren J. Wilkinson, David Lydall, Jennifer Hallinan, Anil Wipat	2011	6
20	MaveQuest: a web resource for planning experimental tests of human variant effects Bioinformatics ·Da Kuang, Jochen Weile, Roujia Li, Tom W Ouellette, Jarry A Barber, Frederick P. Roth	2020	6

About Jochen Weile

Jochen Weile is a scholar working on Genetics, Molecular Biology, Cancer Research, Clinical Biochemistry and Information Systems and Management, having authored 27 papers that have together received 655 indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (8 papers), Genomics and Rare Diseases (8 papers), Bioinformatics and Genomic Networks (5 papers), CRISPR and Genetic Engineering (4 papers), Biomedical Text Mining and Ontologies (4 papers), Cancer Genomics and Diagnostics (3 papers), Ubiquitin and proteasome pathways (3 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Genetics (285 citations), Molecular Biology (488 citations), Cancer Research (83 citations), Computational Theory and Mathematics (48 citations) and Aging (4 citations). Jochen Weile has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Frederick P. Roth, Douglas M. Fowler, Alan F. Rubin, Song Sun, Yingzhou Wu, Lea M. Starita, Jay Shendure, Anthony T. Papenfuss, Roujia Li and Anil Wipat. Their work appears in journals such as Bioinformatics, The American Journal of Human Genetics, Berichte aus der medizinischen Informatik und Bioinformatik/Journal of integrative bioinformatics, Human Mutation and Genome biology.

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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