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Robin van der Lee
Robin van der Lee
AbCellera Biologics
Verified email at cmmt.ubc.ca - Homepage
Title
Cited by
Cited by
Year
Classification of intrinsically disordered regions and proteins
R van der Lee, M Buljan, B Lang, RJ Weatheritt, GW Daughdrill, ...
Chemical reviews 114 (13), 6589-6631, 2014
19622014
JASPAR 2020: update of the open-access database of transcription factor binding profiles
O Fornes, JA Castro-Mondragon, A Khan, R van der Lee, X Zhang, ...
Nucleic acids research 48 (D1), D87-D92, 2020
16982020
JASPAR 2018: update of the open-access database of transcription factor binding profiles and its web framework
A Khan, O Fornes, A Stigliani, M Gheorghe, JA Castro-Mondragon, ...
Nucleic acids research 46 (D1), D260-D266, 2018
16072018
Intrinsically disordered proteins: regulation and disease
MM Babu, R van der Lee, NS de Groot, J Gsponer
Current opinion in structural biology 21 (3), 432-440, 2011
6682011
LY-CoV1404 (bebtelovimab) potently neutralizes SARS-CoV-2 variants
K Westendorf, S Žentelis, L Wang, D Foster, P Vaillancourt, M Wiggin, ...
Cell reports 39 (7), 2022
3412022
Intrinsically Disordered Segments Affect Protein Half-Life in the Cell and during Evolution
R van der Lee, B Lang, K Kruse, J Gsponer, NS de Groot, MA Huynen, ...
Cell reports 8 (6), 1832-1844, 2014
2262014
TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome
NJ Lambacher, AL Bruel, TJP van Dam, K Szymańska, GG Slaats, ...
Nature cell biology 18 (1), 122-131, 2016
1372016
CiliaCarta: an integrated and validated compendium of ciliary genes
TJP Van Dam, J Kennedy, R Van Der Lee, E De Vrieze, KA Wunderlich, ...
PloS one 14 (5), e0216705, 2019
1142019
The RIG-I-like helicase receptor MDA5 (IFIH1) is involved in the host defense against Candida infections
M Jaeger, R van der Lee, SC Cheng, MD Johnson, V Kumar, A Ng, ...
European Journal of Clinical Microbiology & Infectious Diseases 34 (5), 963-974, 2015
892015
Genome-scale detection of positive selection in nine primates predicts human-virus evolutionary conflicts
R Van der Lee, L Wiel, TJP Van Dam, MA Huynen
Nucleic Acids Research 45 (18), 10634–10648, 2017
762017
Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related Encephalopathy
CDM van Karnebeek, RJ Ramos, XY Wen, M Tarailo-Graovac, ...
The American Journal of Human Genetics 105 (3), 534-548, 2019
572019
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease
M Sharma, D Leung, M Momenilandi, LCW Jones, L Pacillo, AE James, ...
Journal of Experimental Medicine 220 (5), e20221755, 2023
422023
Probabilistic data integration identifies reliable gametocyte-specific proteins and transcripts in malaria parasites
L Meerstein-Kessel, R van der Lee, W Stone, K Lanke, DA Baker, P Alano, ...
Scientific reports 8 (1), 410, 2018
402018
Deregulated regulators: disease-causing cis variants in transcription factor genes
R van Der Lee, S Correard, WW Wasserman
Trends in Genetics 36 (7), 523-539, 2020
342020
Integrative genomics-based discovery of novel regulators of the innate antiviral response
R van der Lee, Q Feng, MA Langereis, R Ter Horst, R Szklarczyk, ...
PLoS computational biology 11 (10), e1004553, 2015
232015
The role of clinical response to treatment in determining pathogenicity of genomic variants
JJ Shen, SB Wortmann, L de Boer, LAJ Kluijtmans, MCDG Huigen, J Koch, ...
Genetics in Medicine 23 (3), 581-585, 2021
182021
Transcriptome analysis of complex I-deficient patients reveals distinct expression programs for subunits and assembly factors of the oxidative phosphorylation system
R van der Lee, R Szklarczyk, J Smeitink, HJM Smeets, MA Huynen, ...
BMC genomics 16, 1-13, 2015
142015
De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy
KM Riedhammer, S Stockler, R Ploski, M Wenzel, B Adis-Dutschmann, ...
Brain 144 (2), 411-419, 2021
132021
Adult GAMT deficiency: A literature review and report of two siblings
BP Modi, HN Khan, R van der Lee, M Wasim, CA Haaxma, PA Richmond, ...
Molecular Genetics and Metabolism Reports 27, 100761, 2021
102021
Curation and bioinformatic analysis of strabismus genes supports functional heterogeneity and proposes candidate genes with connections to RASopathies
XC Ye, R van der Lee, WW Wasserman
Gene 697, 213-226, 2019
72019
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