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Lista de obras de Mark McCormack

A genome-wide association study of recipient genotype and medium-term kidney allograft function

artículo científico publicado en 2013

A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine

artículo científico publicado en 2019

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy

artículo científico publicado en 2021

Association of CYP3A variants with kidney transplant outcomes

artículo científico publicado en 2015

Development of a genomics module within an epilepsy-specific electronic health record: Toward genomic medicine in epilepsy care

artículo científico publicado en 2019

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy

artículo científico publicado en 2012

Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies

artículo científico publicado en 2014

Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients

artículo científico publicado en 2017

Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions

artículo científico publicado en 2012

Genomic and clinical predictors of lacosamide response in refractory epilepsies

artículo científico publicado en 2019

HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans

artículo científico publicado en 2011

Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders

artículo científico publicado en 2010

Pharmacogenomics and epilepsy: the road ahead

artículo científico

Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

article

Response 2 to pharmacogenetic screening to prevent carbamazepine-induced toxic epidermal necrolysis and Stevens-Johnson syndrome: a critical appraisal

article

TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural function

scientific journal article

Testing association of rare genetic variants with resistance to three common antiseizure medications

artículo científico publicado en 2020

The impact of ERBB-family germline single nucleotide polymorphisms on survival response to adjuvant trastuzumab treatment in HER2-positive breast cancer

artículo científico publicado en 2016

Tibetans living at sea level have a hyporesponsive hypoxia-inducible factor system and blunted physiological responses to hypoxia

artículo científico publicado en 2013

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