Author details

Full Name

Roland Krause

Affiliation

University of Luxembourg

ORCID

Career Start Year

2002

Papers

H Index

Expertise

CM4AI Collaborator

Timothy Clark (CM4AI)

PMID	Paper Title	Journal Title	Published Year
35298028	A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam.	Epilepsia	2022
35620985	Benchmarking of univariate pleiotropy detection methods applied to epilepsy.	Hum Mutat	2022
36467455	Individualised prediction of drug resistance and seizure recurrence after medication withdrawal in people with juvenile myoclonic epilepsy: A systematic review and individual participant data meta-analysis.	EClinicalMedicine	2022
36088682	Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies.	EBioMedicine	2022
33264411	The Human Phenotype Ontology in 2021.	Nucleic Acids Res	2021
33731876	Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders.	Genet Med	2021
34571366	Distinct gene-set burden patterns underlie common generalized and focal epilepsies.	EBioMedicine	2021
34018700	Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy.	Ann Clin Transl Neurol	2021
34177598	Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications.	Front Pharmacol	2021
34031551	Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical data.	Eur J Hum Genet	2021
33949685	Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable.	Epilepsia	2021
32141622	Testing association of rare genetic variants with resistance to three common antiseizure medications.	Epilepsia	2020
32972997	Gene selection for optimal prediction of cell position in tissues from single-cell transcriptomics data.	Life Sci Alliance	2020
32853554	Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies.	Am J Hum Genet	2020
32308125	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	Pharmacogenomics	2020
32437350	Ten simple rules for making training materials FAIR.	PLoS Comput Biol	2020
30868120	A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.	Epilepsia Open	2019
31819912	Genomic and clinical predictors of lacosamide response in refractory epilepsies.	Epilepsia Open	2019
31440723	Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy.	Epilepsia Open	2019
29288229	Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.	Neurology	2018
30148849	Rare gene deletions in genetic generalized and Rolandic epilepsies.	PLoS One	2018
30033060	Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control study.	Lancet Neurol	2018
29358611	Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.	Eur J Hum Genet	2018
29398565	Personalized risk prediction of postoperative cognitive impairment -Â rationale for the EU-funded BioCog project.	Eur Psychiatry	2018
27899602	The Human Phenotype Ontology in 2017.	Nucleic Acids Res	2017
29053855	Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features.	Brain	2017
28857179	Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis.	Epilepsia	2017
28576708	A systems level analysis of epileptogenesis-associated proteome alterations.	Neurobiol Dis	2017
27079753	Crowdsourced estimation of cognitive decline and resilience in Alzheimer's disease.	Alzheimers Dement	2016
26888283	70S-scanning initiation is a novel and frequent initiation mode of ribosomal translation in bacteria.	Proc Natl Acad Sci U S A	2016
26990884	Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes.	PLoS One	2016
25751627	De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.	Nat Genet	2015
26106326	Biomarkers of postoperative delirium and cognitive dysfunction.	Front Aging Neurosci	2015
26220384	Investigation of GRIN2A in common epilepsy phenotypes.	Epilepsy Res	2015
25783594	CHD2 variants are a risk factor for photosensitivity in epilepsy.	Brain	2015
22759421	Exploring biological interaction networks with tailored weighted quasi-bicliques.	BMC Bioinformatics	2012
21358006	Selecting oligonucleotide probes for whole-genome tiling arrays with a cross-hybridization potential.	IEEE/ACM Trans Comput Biol Bioinform	2011
21686311	Cocos: Constructing multi-domain protein phylogenies.	PLoS Curr	2011
21282868	The plexus model for the inference of ancestral multidomain proteins.	IEEE/ACM Trans Comput Biol Bioinform	2011
20126524	Live Coverage of Intelligent Systems for Molecular Biology/European Conference on computational biology (ISMB/ECCB) 2009.	PLoS Comput Biol	2010
20126525	Live coverage of scientific conferences using web technologies.	PLoS Comput Biol	2010
19180175	Microblogging the ISMB: a new approach to conference reporting.	PLoS Comput Biol	2009
18445686	EML3 is a nuclear microtubule-binding protein required for the correct alignment of chromosomes in metaphase.	J Cell Sci	2008
18989043	Efficient algorithms for the computational design of optimal tiling arrays.	IEEE/ACM Trans Comput Biol Bioinform	2008
18312844	Mutation in the transcriptional regulator PhoP contributes to avirulence of Mycobacterium tuberculosis H37Ra strain.	Cell Host Microbe	2008
17224916	Identification of tightly regulated groups of genes during Drosophila melanogaster embryogenesis.	Mol Syst Biol	2007
18269697	Semi-supervised learning for the identification of syn-expressed genes from fused microarray and in situ image data.	BMC Bioinformatics	2007
18093306	Identifying protein complexes directly from high-throughput TAP data with Markov random fields.	BMC Bioinformatics	2007
16429126	Proteome survey reveals modularity of the yeast cell machinery.	Nature	2006
17094242	Identifying protein complexes in high-throughput protein interaction screens using an infinite latent feature model.	Pac Symp Biocomput	2006

1 - 50 of 56

Alberto Paccanaro

University of London

Career Start Year 2005

Number of shared co-authors 5

Fred P Davis

Howard Hughes Medical Institute

Career Start Year 2004

Number of shared co-authors 2

Madan Mohan Babu

St. Jude Children's Research Hospital

Career Start Year 2002

Number of shared co-authors 3

Haiyuan Yu

Weill Institute for Cell and Molecular Biology, Cornell University

Career Start Year 2001

Number of shared co-authors 2

Gary D Bader

University of Toronto

Career Start Year 2000

Number of shared co-authors 9

Roded Sharan

Tel Aviv University

Career Start Year 2000

Number of shared co-authors 1

Frederick P Roth

University of Toronto

Career Start Year 1998

Number of shared co-authors 6

Benno Schwikowski

Center for Bioinformatics, Institut Pasteur CNRS

Career Start Year 1997

Number of shared co-authors 3

Trey Ideker (CM4AI)

University of California San Diego

Career Start Year 1996

Number of shared co-authors 8

Ron Shamir

Tel Aviv University

Career Start Year 1995

Number of shared co-authors 0

Ralf Zimmer

Ludwig-Maximilians-Universitat Munchen

Career Start Year 1995

Number of shared co-authors 5

Ioannis Xenarios

University of Lausanne

Career Start Year 1994

Number of shared co-authors 12

Steven E Brenner

University of California berkeley

Career Start Year 1994

Number of shared co-authors 10

Bonnie Berger

Massachusetts Institute of Technology

Career Start Year 1994

Number of shared co-authors 2

Joel S Bader

Johns Hopkins University

Career Start Year 1993

Number of shared co-authors 7

Edward M Marcotte

University of Texas

Career Start Year 1993

Number of shared co-authors 3

Bianca Habermann

Aix Marseille University, CNRS, Turing Center for Living Systems

Career Start Year 1993

Number of shared co-authors 2

Jason E McDermott

Pacific Northwest National Laboratory

Career Start Year 1993

Number of shared co-authors 0

Simon Kasif

Boston University

Career Start Year 1993

Number of shared co-authors 1

Zhiping Weng

University of Massachusetts Medical School

Career Start Year 1992

Number of shared co-authors 6

Miguel A Andrade-Navarro

Institute of Organismic and Molecular Evolution, Johannes Gutenberg University

Career Start Year 1991

Number of shared co-authors 5

Robert Gentleman

Center for Computational Biomedicine, Harvard Medical School

Career Start Year 1991

Number of shared co-authors 2

Mark Gerstein

Yale University

Career Start Year 1991

Number of shared co-authors 14

Andreas Beyer

University of Cologne

Career Start Year 1991

Number of shared co-authors 4

Marc Vidal

Blavatnik Institute, Harvard Medical School

Career Start Year 1989

Number of shared co-authors 4

S??ren Brunak

Novo Nordisk Foundation Center for Protein Research, University of Copenhagen

Career Start Year 1988

Number of shared co-authors 8

Michal Linial

Institute of Life Sciences, The Hebrew University of Jerusalem

Career Start Year 1986

Number of shared co-authors 2

Alfonso Valencia

Josep Carreras Leukaemia Research Institute (IJC)

Career Start Year 1986

Number of shared co-authors 27

Richard Bonneau

Center for Computational Biology (CCB), Flatiron Institute, Simons Foundation

Career Start Year 1983

Number of shared co-authors 3

Yves Moreau

KU Leuven - University of Leuven

Career Start Year 1967

Number of shared co-authors 11

row(s) 1 - 30 of 30

Sanjay M Sisodiya

UCL Institute of Neurology

Co-authored papers 13

Josemir W Sander

West China Hospital of Sichuan University

Co-authored papers 12

Chantal Depondt

Hopital Universitaire de Bruxelles - Hopital Erasme

Co-authored papers 11

Gianpiero L Cavalleri

School of Pharmacy and Biomolecular Sciences, Ireland FutureNeuro SFI Research Centre

Co-authored papers 11

Norman Delanty

FutureNeuro SFI Research Centre, The Royal College of Surgeons in Ireland

Co-authored papers 10

Ingo Helbig

Children's Hospital of Philadelphia

Co-authored papers 10

Michael R Johnson

Imperial College London

Co-authored papers 9

Peer Bork

University of Wurzburg

Co-authored papers 6

Terence J O'Brien

Monash University

Co-authored papers 6

David Lewis-Smith

Translational and Clinical Research Institute, Newcastle University

Co-authored papers 5

Peter D Galer

Children's Hospital of Philadelphia

Co-authored papers 5

Reinhard Schneider

Co-authored papers 4

Aarno Palotie

Co-authored papers 4

Hreinn Stefansson

Co-authored papers 3

Lars Juhl Jensen

Novo Nordisk Foundation Center for Protein Research, University of Copenhagen

Co-authored papers 3

Christian von Mering

Co-authored papers 3

Andr?? G Uitterlinden

Erasmus University Medical Center

Co-authored papers 3

Melissa A Haendel

American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison

Co-authored papers 2

Thomas Dorn

Universitat Rostock

Co-authored papers 2

Anne T Nies

and University of Tuebingen, University of Tuebingen

Co-authored papers 2

Ana Rath

INSERM

Co-authored papers 2

Colin P Doherty

St James's Hospital