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Author Details
Full Name
Robert B Russell
Affiliation
Heidelberg University
ORCID
Career Start Year
1991
Papers
167
H Index
69
Expertise
CM4AI Collaborator
Andrej Sali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36776558
A targeted multi-proteomics approach generates a blueprint of the ciliary ubiquitinome.
Front Cell Dev Biol
2023
35522148
Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B-cell lymphomas.
Haematologica
2023
37371694
Emerging Trends in the Field of Inflammation and Proteinopathy in ALS/FTD Spectrum Disorder.
Biomedicines
2023
36994552
Genomic landscape of follicular lymphoma across a wide spectrum of clinical behaviors.
Hematol Oncol
2023
36354106
Biochemically validated structural model of the 15-subunit intraflagellar transport complex IFT-B.
EMBO J
2022
35639758
PRECOGx: exploring GPCR signaling mechanisms with deep protein representations.
Nucleic Acids Res
2022
36454823
The human signal peptidase complex acts as a quality control enzyme for membrane proteins.
Science
2022
36075934
Never-homozygous genetic variants in healthy populations are potential recessive disease candidates.
NPJ Genom Med
2022
35960718
The S-palmitoylome and DHHC-PAT interactome of Drosophila melanogaster S2R+ cells indicate a high degree of conservation to mammalian palmitoylomes.
PLoS One
2022
34358547
Next Generation Protein Structure Predictions and Genetic Variant Interpretation.
J Mol Biol
2021
33646271
RhoGAP19D inhibits Cdc42 laterally to control epithelial cell shape and prevent invasion.
J Cell Biol
2021
34076240
Mechnetor: a web server for exploring protein mechanism and the functional context of genetic variants.
Nucleic Acids Res
2021
33055194
The Interaction of Munc18-1 Helix 11 and 12 with the Central Region of the VAMP2 SNARE Motif Is Essential for SNARE Templating and Synaptic Transmission.
eNeuro
2020
31761904
Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patients.
Genet Med
2020
30567752
The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma.
Blood
2019
31748534
Molecular switch from MYC to MYCN expression in MYC protein negative Burkitt lymphoma cases.
Blood Cancer J
2019
30926794
Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma.
Nat Commun
2019
30923826
EZHIP/CXorf67 mimics K27M mutated oncohistones and functions as an intrinsic inhibitor of PRC2 function in aggressive posterior fossa ependymoma.
Neuro Oncol
2019
31095607
CiliaCarta: An integrated and validated compendium of ciliary genes.
PLoS One
2019
31143927
PRECOG: PREdicting COupling probabilities of G-protein coupled receptors.
Nucleic Acids Res
2019
30967556
Defective homologous recombination DNA repair as therapeutic target in advanced chordoma.
Nat Commun
2019
31171722
Illuminating the Onco-GPCRome: Novel G protein-coupled receptor-driven oncocrine networks and targets for cancer immunotherapy.
J Biol Chem
2019
30485545
Understanding the role of genetic variability in LRRK2 in Indian population.
Mov Disord
2019
29238877
Cryptogenic cholestasis in young and adults: ATP8B1, ABCB11, ABCB4, and TJP2 gene variants analysis by high-throughput sequencing.
J Gastroenterol
2018
30315099
Studying how genetic variants affect mechanism in biological systems.
Essays Biochem
2018
29364530
Cancer genetics meets biomolecular mechanism-bridging an age-old gulf.
FEBS Lett
2018
28743795
Capturing protein communities by structural proteomics in a thermophilic eukaryote.
Mol Syst Biol
2017
28346509
Systematic identification of phosphorylation-mediated protein interaction switches.
PLoS Comput Biol
2017
28466873
Corrigendum: Insights into cancer severity from biomolecular interaction mechanisms.
Sci Rep
2017
29254951
Landscape of nuclear transport receptor cargo specificity.
Mol Syst Biol
2017
28986545
Genetic variants affecting equivalent protein family positions reflect human diversity.
Sci Rep
2017
26917488
Genes encoding members of the JAK-STAT pathway or epigenetic regulators are recurrently mutated in T-cell prolymphocytic leukaemia.
Br J Haematol
2016
27698488
Insights into cancer severity from biomolecular interaction mechanisms.
Sci Rep
2016
27173435
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms.
Nat Commun
2016
27549192
Mutagenesis of N-terminal residues of feline foamy virus Gag reveals entirely distinct functions during capsid formation, particle assembly, Gag processing and budding.
Retrovirology
2016
25189415
The mutational pattern of primary lymphoma of the central nervous system determined by whole-exome sequencing.
Leukemia
2015
26437030
DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control.
Nat Genet
2015
26714646
KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome.
Genome Biol
2015
26173642
The PCBP1 gene encoding poly(rC) binding protein I is recurrently mutated in Burkitt lymphoma.
Genes Chromosomes Cancer
2015
25392414
Mechismo: predicting the mechanistic impact of mutations and modifications on molecular interactions.
Nucleic Acids Res
2015
24446122
Recurrent mutation of JAK3 in T-cell prolymphocytic leukemia.
Genes Chromosomes Cancer
2014
25255318
Characterizing protein interactions employing a genome-wide siRNA cellular phenotyping screen.
PLoS Comput Biol
2014
25060813
SMARCA4-mutated atypical teratoid/rhabdoid tumors are associated with inherited germline alterations and poor prognosis.
Acta Neuropathol
2014
25044415
Recurrent RHOA mutations in pediatric Burkitt lymphoma treated according to the NHL-BFM protocols.
Genes Chromosomes Cancer
2014
24398325
A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma.
Blood
2014
23748378
Molecular dissection of human Argonaute proteins by DNA shuffling.
Nat Struct Mol Biol
2013
22110041
ProtChemSI: a network of protein-chemical structural interactions.
Nucleic Acids Res
2012
23143595
Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.
Nat Genet
2012
22832583
Dissecting the genomic complexity underlying medulloblastoma.
Nature
2012
22884951
Negative protein-protein interaction datasets derived from large-scale two-hybrid experiments.
Methods
2012
1 - 50 of 167
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German Cancer Research Center (DKFZ)
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