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Author Details
Full Name
Alan Medlar
Affiliation
Institute of Biotechnology, University of Helsinki
ORCID
Career Start Year
2010
Papers
21
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
32712245
Metatranscriptomic assessment of burn wound infection clearance.
Clin Microbiol Infect
2021
31882397
TRAP1 chaperone protein mutations and autoinflammation.
Life Sci Alliance
2019
31744546
The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens.
Genome Biol
2019
28534454
Opportunities and challenges in metabarcoding approaches for helminth community identification in wild mammals.
Parasitology
2018
30064374
TOPAZ: asymmetric suffix array neighbourhood search for massive protein databases.
BMC Bioinformatics
2018
29741643
PANNZER2: a rapid functional annotation web server.
Nucleic Acids Res
2018
29762724
AAI-profiler: fast proteome-wide exploratory analysis reveals taxonomic identity, misclassification and contamination.
Nucleic Acids Res
2018
27994071
Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1.
J Exp Med
2017
28961780
HaploForge: a comprehensive pedigree drawing and haplotype visualization web application.
Bioinformatics
2017
27938331
Robust multi-group gene set analysis with few replicates.
BMC Bioinformatics
2016
26635364
Wasabi: An Integrated Platform for Evolutionary Sequence Analysis and Data Visualization.
Mol Biol Evol
2016
25892063
Tracking year-to-year changes in intestinal nematode communities of rufous mouse lemurs (Microcebus rufus).
Parasitology
2015
25433763
Séance: reference-based phylogenetic analysis for 18S rRNA studies.
BMC Evol Biol
2014
22849749
Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.
Oral Dis
2013
23431073
Phospholipase A2 receptor (PLA2R1) sequence variants in idiopathic membranous nephropathy.
J Am Soc Nephrol
2013
23424103
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia.
Ann Neurol
2013
23239673
SwiftLink: parallel MCMC linkage analysis using multicore CPU and GPU.
Bioinformatics
2013
21617915
Genetic testing in renal disease.
Pediatr Nephrol
2012
23434854
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.
Nephron Physiol
2012
21323541
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.
N Engl J Med
2011
19959600
Cystinosis and mickey mouse.
Nephrol Dial Transplant
2010
1 - 21 of 21
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row(s) 1 - 30 of 30
Collaborators
Liisa Holm
Institute of Biotechnology, University of Helsinki
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6
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Great Ormond Street Hospital for Children, NHS Foundation Trust
Co-authored papers
4
Petri T??r??nen
Institute of Biotechnology, University of Helsinki
Co-authored papers
4
Ari Löytynoja
Co-authored papers
3
Marieke J H Coenen
Co-authored papers
2
Naihui Zhou
The First Affiliated Hospital of Soochow University
Co-authored papers
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Itamar Borukhov
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Co-authored papers
1
Maria J Martin
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers
1
Md Nafiz Hamid
Iowa State University
Co-authored papers
1
Larry Davis
Co-authored papers
1
Radoslav Davidovic
Institute of Nuclear Sciences Vinca, University of Belgrade
Co-authored papers
1
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University of California Berkeley
Co-authored papers
1
Sa??o D??eroski
Jozef Stefan Institute
Co-authored papers
1
Domenico Cozzetto
Imperial College London
Co-authored papers
1
Marco Mesiti
Universita degli Studi di Milano
Co-authored papers
1
Neven Sumonja
Institute of Nuclear Sciences VINCA, University of Belgrade
Co-authored papers
1
Magdalena Kotlicka-Antczak
Medical University of Lodz
Co-authored papers
1
Alan J Medlar
Co-authored papers
1
Rui Fa
University College London
Co-authored papers
1
Kevin Bryson
University of Glasgow
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1
Sabeur Aridhi
Universite de Lorraine, CNRS
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