| Year |
Citation |
Score |
| 2018 |
Medlar AJ, Törönen P, Holm L. AAI-profiler: fast proteome-wide exploratory analysis reveals taxonomic identity, misclassification and contamination. Nucleic Acids Research. PMID 29762724 DOI: 10.1093/nar/gky359 |
0.381 |
|
| 2018 |
Törönen P, Medlar A, Holm L. PANNZER2: a rapid functional annotation web server. Nucleic Acids Research. PMID 29741643 DOI: 10.1093/Nar/Gky350 |
0.398 |
|
| 2018 |
Aivelo T, Medlar A, Löytynoja A, Laakkonen J, Jernvall J. Metabarcoding Gastrointestinal Nematodes in Sympatric Endemic and Nonendemic Species in Ranomafana National Park, Madagascar International Journal of Primatology. 39: 49-64. DOI: 10.1007/s10764-017-0010-x |
0.563 |
|
| 2017 |
Aivelo T, Medlar A. Opportunities and challenges in metabarcoding approaches for helminth community identification in wild mammals. Parasitology. 1-14. PMID 28534454 DOI: 10.1017/S0031182017000610 |
0.369 |
|
| 2017 |
Medlar A, Törönen P, Zosa E, Holm L. PANNZER 2: annotate a complete proteome in minutes! F1000research. 6. DOI: 10.7490/F1000Research.1114786.1 |
0.324 |
|
| 2016 |
Mishra PP, Medlar A, Holm L, Törönen P. Robust multi-group gene set analysis with few replicates. Bmc Bioinformatics. 17: 526. PMID 27938331 DOI: 10.1186/S12859-016-1403-0 |
0.33 |
|
| 2015 |
Veidenberg A, Medlar A, Löytynoja A. Wasabi: an integrated platform for evolutionary sequence analysis and data visualisation. Molecular Biology and Evolution. PMID 26635364 DOI: 10.1093/Molbev/Msv333 |
0.499 |
|
| 2015 |
Aivelo T, Medlar A, Löytynoja A, Laakkonen J, Jernvall J. Tracking year-to-year changes in intestinal nematode communities of rufous mouse lemurs (Microcebus rufus). Parasitology. 142: 1095-107. PMID 25892063 DOI: 10.1017/S0031182015000438 |
0.617 |
|
| 2015 |
Aivelo T, Medlar A, Löytynoja A, Laakkonen J, Jernvall J. Tracking year-to-year changes in intestinal nematode communities of rufous mouse lemurs (Microcebus rufus) Parasitology. 142: 1095-1107. DOI: 10.1017/S0031182015000438 |
0.574 |
|
| 2014 |
Medlar A, Aivelo T, Löytynoja A. Séance: reference-based phylogenetic analysis for 18S rRNA studies. Bmc Evolutionary Biology. 14: 235. PMID 25433763 DOI: 10.1186/S12862-014-0235-7 |
0.666 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2018 |
Medlar A, Holm L. TOPAZ: asymmetric suffix array neighbourhood search for massive protein databases. Bmc Bioinformatics. 19: 278. PMID 30064374 DOI: 10.1186/S12859-018-2290-3 |
0.279 |
|
| 2020 |
Medlar A, Glowacka D. "Exploratory search: user behaviour and search engine adaptation" by Alan Medlar and Dorota G?owacka with Martin Vesely as coordinator. Acm Sigweb Newsletter. 2019: 1-3. DOI: 10.1145/3352683.3352687 |
0.268 |
|
| 2017 |
Tekman M, Medlar A, Mozere M, Kleta R, Stanescu H. HaploForge: A Comprehensive Pedigree Drawing and Haplotype Visualisation Web Application. Bioinformatics (Oxford, England). PMID 28961780 DOI: 10.1093/Bioinformatics/Btx510 |
0.254 |
|
| 2013 |
Coenen MJ, Hofstra JM, Debiec H, Stanescu HC, Medlar AJ, Stengel B, Boland-Augé A, Groothuismink JM, Bockenhauer D, Powis SH, Mathieson PW, Brenchley PE, Kleta R, Wetzels JF, Ronco P. Phospholipase A2 receptor (PLA2R1) sequence variants in idiopathic membranous nephropathy. Journal of the American Society of Nephrology : Jasn. 24: 677-83. PMID 23431073 DOI: 10.1681/ASN.2012070730 |
0.218 |
|
| 2019 |
Zhou N, Jiang Y, Bergquist TR, Lee AJ, Kacsoh BZ, Crocker AW, Lewis KA, Georghiou G, Nguyen HN, Hamid MN, Davis L, Dogan T, Atalay V, Rifaioglu AS, Dalkıran A, ... ... Medlar AJ, et al. The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens. Genome Biology. 20: 244. PMID 31744546 DOI: 10.1186/S13059-019-1835-8 |
0.191 |
|
| 2020 |
Ojala T, Lindford A, Savijoki K, Lagus H, Tommila J, Medlar A, Kuusela P, Varmanen P, Holm L, Vuola J, Kankuri E, Kankainen M. Metatranscriptomic assessment of burn wound infection clearance. Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases. PMID 32712245 DOI: 10.1016/J.Cmi.2020.07.021 |
0.167 |
|
| 2013 |
Nibali L, Medlar A, Stanescu H, Kleta R, Darbar U, Donos N. Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis Oral Diseases. 19: 100-105. PMID 22849749 DOI: 10.1111/j.1601-0825.2012.01965.x |
0.142 |
|
| 1991 |
Kahle B, Medlar A. An information system for corporate users: Wide area information servers Online (Wilton, Connecticut). 15: 56-60. |
0.139 |
|
| 2013 |
Medlar A, Głowacka D, Stanescu H, Bryson K, Kleta R. SwiftLink: Parallel MCMC linkage analysis using multicore CPU and GPU Bioinformatics. 29: 413-419. PMID 23239673 DOI: 10.1093/bioinformatics/bts704 |
0.127 |
|
| 2013 |
Hersheson J, Mencacci NE, Davis M, MacDonald N, Trabzuni D, Ryten M, Pittman A, Paudel R, Kara E, Fawcett K, Plagnol V, Bhatia KP, Medlar AJ, Stanescu HC, Hardy J, et al. Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia. Annals of Neurology. 73: 546-53. PMID 23424103 DOI: 10.1002/Ana.23832 |
0.111 |
|
| 2010 |
Medlar A, Kleta R. Cystinosis and mickey mouse Nephrology Dialysis Transplantation. 25: 1032-1033. PMID 19959600 DOI: 10.1093/ndt/gfp648 |
0.069 |
|
| 2015 |
Athukorala K, Medlar A, Ilves K, Gtowacka D. Balancing exploration and exploitation: Empirical parameterization of exploratory search systems International Conference On Information and Knowledge Management, Proceedings. 19: 1703-1706. DOI: 10.1145/2806416.2806609 |
0.06 |
|
| 2020 |
Standing AS, Hong Y, Paisan-Ruiz C, Omoyinmi E, Medlar A, Stanescu H, Kleta R, Rowcenzio D, Hawkins P, Lachmann H, McDermott MF, Eleftheriou D, Klein N, Brogan PA. TRAP1 chaperone protein mutations and autoinflammation. Life Science Alliance. 3. PMID 31882397 DOI: 10.26508/lsa.201900376 |
0.049 |
|
| 2016 |
Standing AS, Malinova D, Hong Y, Record J, Moulding D, Blundell MP, Nowak K, Jones H, Omoyinmi E, Gilmour KC, Medlar A, Stanescu H, Kleta R, Anderson G, Nanthapisal S, et al. Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1. The Journal of Experimental Medicine. PMID 27994071 DOI: 10.1084/jem.20161228 |
0.035 |
|
| 2012 |
Jaureguiberry G, De la Dure-Molla M, Parry D, Quentric M, Himmerkus N, Koike T, Poulter J, Klootwijk E, Robinette SL, Howie AJ, Patel V, Figueres ML, Stanescu HC, Issler N, Nicholson JK, ... ... Medlar AJ, et al. Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations. Nephron. Physiology. 122: 1-6. PMID 23434854 DOI: 10.1159/000349989 |
0.022 |
|
| 2011 |
Stanescu HC, Arcos-Burgos M, Medlar A, Bockenhauer D, Kottgen A, Dragomirescu L, Voinescu C, Patel N, Pearce K, Hubank M, Stephens HA, Laundy V, Padmanabhan S, Zawadzka A, Hofstra JM, et al. Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. The New England Journal of Medicine. 364: 616-26. PMID 21323541 DOI: 10.1056/NEJMoa1009742 |
0.014 |
|
| 2012 |
Bockenhauer D, Medlar AJ, Ashton E, Kleta R, Lench N. Genetic testing in renal disease Pediatric Nephrology. 27: 873-883. PMID 21617915 DOI: 10.1007/s00467-011-1865-2 |
0.01 |
|
| 2011 |
Głowacka D, Dorard L, Medlar A, Shawe-Taylor J. Prior knowledge in learning finite parameter spaces Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 5591: 199-213. DOI: 10.1007/978-3-642-20169-1_13 |
0.01 |
|
| Hide low-probability matches. |