Skip to Main Content

Author Details

Klaudia Walter
Wellcome Sanger Institute
2004
54
31
PMIDPaper TitleJournal TitlePublished Year
36136759GWAS of genetic factors affecting white blood cell morphological parameters in Sardinians uncovers influence of chromosome 11 innate immunity gene cluster on eosinophil morphology.Hum Mol Genet2023
37596262A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.Nat Commun2023
35288711Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases.Nat Genet2022
35568032Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.Am J Hum Genet2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
34226637Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates.Int J Obes (Lond)2021
33863903Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease.Nat Commun2021
34582791Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.Am J Hum Genet2021
34426706Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases.Nat Med2021
31520489Population-wide copy number variation calling using variant call format files from 6,898 individuals.Genet Epidemiol2020
32888494The Polygenic and Monogenic Basis of Blood Traits and Diseases.Cell2020
32150548The influence of rare variants in circulating metabolic biomarkers.PLoS Genet2020
30692680GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals.Nat Genet2019
29780001Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study.Lancet Haematol2018
29876889Quality Control of Common and Rare Variants.Methods Mol Biol2018
30405126Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.Nat Commun2018
30568165Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.Nat Commun2018
30390057Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.Nat Genet2018
28552196Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.Am J Hum Genet2017
28449691The impact of rare and low-frequency genetic variants in common disease.Genome Biol2017
28235197An Organismal CNV Mutator Phenotype Restricted to Early Human Development.Cell2017
28145424Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom.Eur J Hum Genet2017
27486782Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.Am J Hum Genet2016
27588453Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.Am J Hum Genet2016
27668658Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.Nat Genet2016
27863252The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.Cell2016
27863251Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.Cell2016
27548312A reference panel of 64,976 haplotypes for genotype imputation.Nat Genet2016
27252175A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease.Sci Transl Med2016
25743335Whole-genome sequence-based analysis of thyroid function.Nat Commun2015
26432246An integrated map of structural variation in 2,504 human genomes.Nature2015
26315906An interactive genome browser of association results from the UK10K cohorts project.Bioinformatics2015
26368830Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel.Nat Commun2015
26367797The UK10K project identifies rare variants in health and disease.Nature2015
26367794Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.Nature2015
25989729Erratum: Whole-genome sequence-based analysis of thyroid function.Nat Commun2015
25962519Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.Nat Commun2015
24676807Estimating genome-wide significance for whole-genome sequencing studies.Genet Epidemiol2014
25225788A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.Nat Commun2014
24816252An atlas of genetic influences on human blood metabolites.Nat Genet2014
22344438A systematic survey of loss-of-function variants in human protein-coding genes.Science2012
21293372Mapping copy number variation by population-scale genome sequencing.Nature2011
19812545Origins and functional impact of copy number variation in the human genome.Nature2010
19825173Deep short-read sequencing of chromosome 17 from the mouse strains A/J and CAST/Ei identifies significant germline variation and candidate genes that regulate liver triglyceride levels.Genome Biol2009
18987734Accurate whole human genome sequencing using reversible terminator chemistry.Nature2008
17019080Factors affecting human IgE and IgG responses to allergen-like Schistosoma mansoni antigens: Molecular structure and patterns of in vivo exposure.Int Arch Allergy Immunol2007
17636860Statistical information characterization of conserved non-coding elements in vertebrates.J Bioinform Comput Biol2007
17274809Parallel evolution of conserved non-coding elements that target a common set of developmental regulatory genes from worms to humans.Genome Biol2007
17015735Increased human IgE induced by killing Schistosoma mansoni in vivo is associated with pretreatment Th2 cytokine responsiveness to worm antigens.J Immunol2006
20483234Characterisation of conserved non-coding sequences in vertebrate genomes using bioinformatics, statistics and functional studies.Comp Biochem Physiol Part D Genomics Proteomics2006
  • 1 - 50 of 54

Recommended Authors

Hao Hu
Aerospace Center Hospital
Career Start Year 2011
Number of shared co-authors 4
Manuel A Rivas
Stanford University School of Medicine
Career Start Year 2008
Number of shared co-authors 80
Martin Kircher
Berlin Institute of Health (BIH) at Charite-Universitatsmedizin Berlin
Career Start Year 2008
Number of shared co-authors 16
Jeffrey G Reid
Regeneron Pharmaceuticals, Inc.
Career Start Year 2007
Number of shared co-authors 46
Chad D Huff
University of Texas M.D. Anderson Cancer Center
Career Start Year 2007
Number of shared co-authors 30
Tuuli Lappalainen
Columbia University
Career Start Year 2006
Number of shared co-authors 52
Benjamin F Voight
Perelman School of Medicine, University of Pennsylvania
Career Start Year 2005
Number of shared co-authors 105
Ali Torkamani
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 9
James G D Prendergast
The Roslin Institute, The University of Edinburgh
Career Start Year 2005
Number of shared co-authors 7
Alicia Hawes
Regeneron Pharmaceuticals Inc.
Career Start Year 2004
Number of shared co-authors 46
Tushar Bhangale
Genentech Inc.
Career Start Year 2004
Number of shared co-authors 52
Chris C A Spencer
University of Oxford
Career Start Year 2004
Number of shared co-authors 50
Zolt??n Kutalik
University of Lausanne
Career Start Year 2004
Number of shared co-authors 112
Degui Zhi
University of Texas Health Science Center at Houston
Career Start Year 2004
Number of shared co-authors 46
Sarah S Murray
University of California San Diego Health System
Career Start Year 2004
Number of shared co-authors 91
Vikas Bansal
University of California San Diego
Career Start Year 2004
Number of shared co-authors 3
Yufeng Shen
Columbia University
Career Start Year 2002
Number of shared co-authors 23
Kai Wang
University of Pennsylvania
Career Start Year 2001
Number of shared co-authors 33
Jessica M Maia
Institute for Genomic Medicine, Columbia University
Career Start Year 2001
Number of shared co-authors 3
Ilja M Nolte
University of Groningen, University Medical Center Groningen
Career Start Year 2000
Number of shared co-authors 110
Michael A Eberle
Illumina Inc.
Career Start Year 2000
Number of shared co-authors 14
Joshua D Smith
University of Washington
Career Start Year 1998
Number of shared co-authors 81
Sebastian Z??llner
University of Michigan ann arbor
Career Start Year 1998
Number of shared co-authors 64
Mathieu Lemire
The Hospital for Sick Children
Career Start Year 1997
Number of shared co-authors 31
Shamil R Sunyaev
Harvard Medical School
Career Start Year 1997
Number of shared co-authors 59
Sarah E Hunt
European Bioinformatics Institute
Career Start Year 1997
Number of shared co-authors 104
Simon Heath
Barcelona Institute of Science and Technology (BIST)
Career Start Year 1995
Number of shared co-authors 77
Devin Absher
Kaiser Permanente Research Bank
Career Start Year 1994
Number of shared co-authors 97
Joel N Hirschhorn
Broad Institute of MIT and Harvard
Career Start Year 1988
Number of shared co-authors 123
Kelly A Frazer
University of California, USA Institute for Genomic Medicine
Career Start Year 1967
Number of shared co-authors 39

Collaborators

Nicole Soranzo
Wellcome Sanger Institute
Co-authored papers 31
Adam S Butterworth
British Heart Foundation Cardiovascular Epidemiology Unit, University of Cambridge
Co-authored papers 16
Nicholas J Timpson
Co-authored papers 14
Kousik Kundu
The Wellcome Sanger Institute
Co-authored papers 14
Eleftheria Zeggini
Co-authored papers 14
Richard Durbin
University of Cambridge
Co-authored papers 12
John Danesh
Co-authored papers 11
Shane McCarthy
Wellcome Sanger Institute
Co-authored papers 11
Lu Chen
Co-authored papers 10
John Brent Richards
Lady Davis Institute for Medical Research, Jewish General Hospital
Co-authored papers 10
George Dedoussis
Co-authored papers 9
Willem H Ouwehand
University of Cambridge
Co-authored papers 9
George Davey Smith
University of Bristol
Co-authored papers 9
Tim D Spector
King's College London
Co-authored papers 8
John R B Perry
Co-authored papers 8
Oliver Stegle
Wellcome Sanger Institute
Co-authored papers 7
Paul L Auer
Co-authored papers 7
Lorraine Southam
Co-authored papers 7
Matthew E Hurles
Wellcome Sanger Institute
Co-authored papers 7
Fernando Rivadeneira
University Medical Center Rotterdam
Co-authored papers 6
Claudia Langenberg
Co-authored papers 6
Giovanni Gambaro
Co-authored papers 6
Inês Barroso
Co-authored papers 6
Celia M T Greenwood
Co-authored papers 6
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 6
Giovanni Malerba
Co-authored papers 6
Andrew D Johnson
and Blood Institute
Co-authored papers 6
Cornelia M van Duijn
University of Oxford
Co-authored papers 6
Albert Hofman
Harvard T.H. Chan School of Public Health
Co-authored papers 6
Mattia Frontini
Co-authored papers 6
Release 1.2