Csaba Halmagyi

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

Keren Carss, Gavin Arno, Marie Erwood et al. · The American Journal of Human Genetics · 2016 · 463 citations · Full text

Whole-genome Sequencing, Allelic Variant, Genetic Disorder +11

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

Paul Tuijnenburg, Hana Lango Allen, Siobhan O. Burns et al. · Journal of Allergy and Clinical Immunology · 2018 · 227 citations · Full text

Primary Immunodeficiency, Disease Susceptibility, Immune Cell Development +15

PDX Finder: A portal for patient-derived tumor xenograft model discovery

Nathalie Conte, Jeremy C. Mason, Csaba Halmagyi et al. · Nucleic Acids Research · 2018 · 93 citations · Full text

Engineering, Pathology, Pdx Models +19

Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

James Whitworth, Philip Smith, Jose‐Ezequiel Martín et al. · The American Journal of Human Genetics · 2018 · 70 citations · Full text

Tumor Biology, Somatic Variant, Broad Range +13

Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma

Ekaterina Minskaia, Jesmeen Maimaris, Persephone Jenkins et al. · Journal of Clinical Immunology · 2023 · 38 citations · Full text

Transcription Factor Stat6, Immunology, Pathology +16