Výsledky vyhledávání - Morris A. Swertz
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Systematic reanalysis of genomic data by diagnostic laboratories: a scoping review of ethical, economic, legal and (psycho)social implications Autor Marije A. van der Geest, Els Maeckelberghe, Mariëlle van Gijn, Anneke Lucassen, Morris A. Swertz, Irene M. van Langen, Mirjam Plantinga
Vydáno 2024Revisão -
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Complex nature of SNP genotype effects on gene expression in primary human leucocytes Autor Graham Heap, Gosia Trynka, Ritsert C. Jansen, Marcel Bruinenberg, Morris A. Swertz, Lotte C. Dinesen, Karen A. Hunt, Cisca Wijmenga, David A vanHeel, Lude Franke
Vydáno 2009Artigo -
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Toward Global Biobank Integration by Implementation of the Minimum Information About BIobank Data Sharing (MIABIS 2.0 Core) Autor Roxana Merino-Martinez, Loreana Norlin, David van Enckevort, Gabriele Anton, Simone Schuffenhauer, Kaisa Silander, Linda Mook, Petr Holub, Raffael Bild, Morris A. Swertz, Jan‐Eric Litton
Vydáno 2016Artigo -
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The phenotypic spectrum of proximal 6q deletions based on a large cohort derived from social media and literature reports Autor Aafke Engwerda, Barbara Frentz, A. Lya den Ouden, Boudien Flapper, Morris A. Swertz, Erica H. Gerkes, Mirjam Plantinga, Trijnie Dijkhuizen, Conny M.A. van Ravenswaaij‐Arts
Vydáno 2018Artigo -
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Habitual dietary intake of IBD patients differs from population controls: a case–control study Autor Vera Peters, Ettje F. Tigchelaar-Feenstra, Floris Imhann, Jackie Dekens, Morris A. Swertz, Lude Franke, Cisca Wijmenga, Rinse K. Weersma, Behrooz Z. Alizadeh, Gerard Dijkstra, Marjo Campmans‐Kuijpers
Vydáno 2020Artigo -
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Lack of Association Between Genetic Variants at ACE2 and TMPRSS2 Genes Involved in SARS-CoV-2 Infection and Human Quantitative Phenotypes Autor Esteban A. Lopera-Maya, Adriaan van der Graaf, Pauline Lanting, Marije van der Geest, Jingyuan Fu, Morris A. Swertz, Lude Franke, Cisca Wijmenga, Patrick Deelen, Alexandra Zhernakova, Serena Sanna
Vydáno 2020Artigo -
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<i>MYO5B</i>,<i>STX3</i>, and<i>STXBP2</i>mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update Autor Herschel S. Dhekne, Olena Pylypenko, Arend W. Overeem, Rosaria J Ferreira, K. Joeri van der Velde, Edmond H.H.M. Rings, Carsten Posovszky, Morris A. Swertz, Anne Houdusse, Sven C.D. van IJzendoorn
Vydáno 2017Revisão -
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Population-specific genotype imputations using minimac or IMPUTE2 Autor Jin‐Moo Lee, Alexandros Kanterakis, Patrick Deelen, Mathijs Kattenberg, P. Eline Slagboom, Paul I. W. de Bakker, Cisca Wijmenga, Morris A. Swertz, Dorret I. Boomsma, Cornelia M. van Duijn, Lennart C. Karssen, Jouke‐Jan Hottenga
Vydáno 2015Artigo -
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Inter-individual variability and genetic influences on cytokine responses to bacteria and fungi Autor Yang Li, Marije Oosting, Patrick Deelen, Isis Ricaño-Ponce, Sanne P. Smeekens, Martin Jaeger, Vasiliki Matzaraki, Morris A. Swertz, Ramnik J. Xavier, Lude Franke, Cisca Wijmenga, Leo A. B. Joosten, Vinod Kumar, Mihai G. Netea
Vydáno 2016Artigo -
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New workflow for classification of genetic variants’ pathogenicity applied to hereditary recurrent fevers by the International Study Group for Systemic Autoinflammatory Diseases (I... Autor Marielle E van Gijn, Isabella Ceccherini, Yael Shinar, Ellen C. Carbo, Mariska Slofstra, Juan I. Aróstegui, Guillaume Sarrabay, Dorota Rowczenio, Ebun Omoyımnı, Banu Balcı‐Peynircioğlu, Hal M. Hoffman, Florian Milhavet, Morris A. Swertz, Isabelle Touitou
Vydáno 2018Artigo -
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An Overview and Online Registry of Microvillus Inclusion Disease Patients and their<i>MYO5B</i>Mutations Autor K. Joeri van der Velde, Herschel S. Dhekne, Morris A. Swertz, Serena Sirigu, Virginie Ropars, Petra C. Vinke, Trebor Rengaw, Peter C. van den Akker, Edmond H.H.M. Rings, Anne Houdusse, Sven C.D. van IJzendoorn
Vydáno 2013Revisão -
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SORTA: a system for ontology-based re-coding and technical annotation of biomedical phenotype data Autor Chao Pang, Annet Sollie, Anna Sijtsma, Dennis Hendriksen, Bart Charbon, Mark de Haan, Tommy de Boer, Fleur Kelpin, Jonathan Jetten, Joeri K. van der Velde, Nynke Smidt, Rolf H. Sijmons, Hans L. Hillege, Morris A. Swertz
Vydáno 2015Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Computational biology
Medicine
Genotype
Single-nucleotide polymorphism
Computer science
Bioinformatics
Genome
Genome-wide association study
Gene expression
Internal medicine
Disease
Pathology
Population
Genetic association
Mutation
Imputation (statistics)
Missing data
Phenotype
Quantitative trait locus
1000 Genomes Project
Environmental health
Immunology
Programming language
DNA methylation
Data science
Database
Demography