Associated Papers
Rare genetic variation in fibronectin 1 (FN1) protects against APOEε4 in Alzheimer's disease.
Bhattarai P et al.
Acta Neuropathologica, 2024
38598053 (PubMed )
Supplement: 401_2024_2721_MOESM5_ESM.xlsx › S_Table_2
Mutational landscape of marginal zone B-cell lymphomas of various origin: organotypic alterations and diagnostic potential for assignment of organ origin.
Vela V et al.
Virchows Archiv : an International Journal of Pathology, 2022
34494161 (PubMed )
Supplement: 428_2021_3186_MOESM21_ESM.xlsx › Supplementary_Table_8
The Pathophysiological Link Between Reelin and Autism: Overview and New Insights.
Scala M et al.
Frontiers in Genetics, 2022
Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families.
Van Marcke C et al.
Breast Cancer Research : Bcr, 2020
32295625 (PubMed )
Supplement: 13058_2020_1273_MOESM1_ESM.xlsx › Table_S2
RELN rare variants in myoclonus-dystonia.
Groen JL et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2015
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 289.143
A case of cohesinopathy with a novel de-novo SMC1A splice site mutation.
Hansen J et al.
Clinical Dysmorphology, 2013
Three-cohort targeted gene screening reveals a non-synonymous TRKA polymorphism associated with schizophrenia.
van Schijndel JE et al.
Journal of Psychiatric Research, 2009
Potential genetic variants in schizophrenia: a Bayesian analysis.
Hall H et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry, 2007
Association of Reelin gene polymorphisms with autism.
Serajee FJ et al.
Genomics, 2006
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