Concepedia

Thomas Scerri

TS

29

Publications

2.9K

Citations

24

H-Index

2002

Active since

Affiliations

Walter and Eliza Hall Institute of Medical Research(Current)

The University of Melbourne

University of Oxford

Centre for Human Genetics

Murdoch Children's Research Institute

Thomas Scerri is an author at Walter and Eliza Hall Institute of Medical Research specializing in medicine, genetics, and neurogenetics.

Top concepts

MedicineGeneticsNeurogeneticsNeuroscienceSocial SciencesNeurodevelopmental DisordersPathologyMolecular GeneticsNeurologyGene Expression

Publications per year

2002–2023

29

Publications

29

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration

Silvia Paracchini, Ankur Thomas, Sandra C. de Castro et al. · Human Molecular Genetics · 2006 · 274 citations · Full text

Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency

Manfred Fliegauf, Vanessa L. Bryant, Natalie Frede et al. · The American Journal of Human Genetics · 2015 · 239 citations · Full text

Primary Immunodeficiency, Immunodeficiencies, Immunology +10

An α‐E‐catenin (<i><scp>CTNNA1</scp></i>) mutation in hereditary diffuse gastric cancer

Ian J. Majewski, Irma Kluijt, Annemieke Cats et al. · The Journal of Pathology · 2012 · 216 citations

Cancer Pathology, Family Members, Genetics +17

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

Else Eising, Amaia Carrión-Castillo, Arianna Vino et al. · Molecular Psychiatry · 2018 · 175 citations · Full text

Brain Development, Genetics, Genetic Epidemiology +25

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

Denise Harold, Silvia Paracchini, Thomas Scerri et al. · Molecular Psychiatry · 2006 · 161 citations · Full text

Neurodevelopmental Disorders, Molecular Neuroscience, Developmental Biology +12

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