Lot Snijders Blok

8PUBLICATIONS
17CO-AUTHORS
NeurogeneticsDevelopmental genetics (incl. sex determination)English as a second languageEpigenetics (incl. genome methylation and epigenomics)Biomedical engineering not elsewhere classified
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Publications (8)

|Aug 18, 2026
Genome sequencing reveals high diagnostic yield in children with severe sporadic developmental language disorder.

|Mar 31, 2025
DDX3X-related neurodevelopmental disorder in males - presenting a new cohort of 19 males and a literature review.

Milou G P Kennis, Dmitrijs Rots, Arjan Bouman

|Jul 09, 2021
Speech-language profiles in the context of cognitive and adaptive functioning in SATB2-associated syndrome.

Lot Snijders Blok, Y Max Goosen, Leenke van Haaften

|Oct 28, 2020
Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities.

Lot Snijders Blok, Arianna Vino, Joery den Hoed

|May 04, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Lot Snijders Blok, Justine Rousseau, Joanna Twist

|Feb 17, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Lot Snijders Blok, Justine Rousseau, Joanna Twist

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Frequent Collaborators

6 joint publications

Simon E Fisher

3 joint publications

Ana S A Cohen

3 joint publications

A Micheil Innes

3 joint publications

Hitoshi Kurumizaka