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Peter Heutink

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 31, 2006

CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementiaPatrizia Rizzu, Saskia E van Mil, Burcu Anar, et al.

Journal of Medical Genetics|March 8, 2024

Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insightsBurcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.

BMC Neurology|October 26, 2011

Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case reportConceição Bettencourt, Cristina Santos, Paula Coutinho, et al.

The Journal of Biological Chemistry|May 30, 2006

DJ-1 transcriptionally up-regulates the human tyrosine hydroxylase by inhibiting the sumoylation of pyrimidine tract-binding protein-associated splicing factorNan Zhong, Christina Y Kim, Patrizia Rizzu, et al.

Biorxiv : the Preprint Server for Biology|February 20, 2025

DNA methylation as a contributor to dysregulation of <i>STX6</i> and other frontotemporal lobar degeneration genetic risk-associated lociNaiomi Rambarack, Katherine Fodder, Megha Murthy, et al.

Human Genetics|July 2, 2014

Population and genomic lessons from genetic analysis of two Indian populationsGarima Juyal, Mayukh Mondal, Pierre Luisi, et al.

Acta Neuropathologica Communications|July 5, 2025

DNA methylation as a contributor to dysregulation of STX6 and other frontotemporal Lobar degeneration genetic risk-associated lociNaiomi Rambarack, Katherine Fodder, Megha Murthy, et al.

Brain : a Journal of Neurology|November 16, 2017

Excessive burden of lysosomal storage disorder gene variants in Parkinson's diseaseLaurie A Robak, Iris E Jansen, Jeroen van Rooij, et al.

Journal of Neuropathology and Experimental Neurology|January 6, 2007

The DeltaK280 mutation in MAP tau favors exon 10 skipping in vivoJohn C van Swieten, Iraad F Bronner, Asma Azmani, et al.

Translational Psychiatry|April 11, 2025

A role for astrocytic miR-129-5p in frontotemporal dementiaLalit Kaurani, Ranjit Pradhan, Sophie Schröder, et al.

Pageof 24

Search research articles

Showing results (41-50 of 240) with videos related to

Sort By:

Pageof 24

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 31, 2006

CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementiaPatrizia Rizzu, Saskia E van Mil, Burcu Anar, et al.

Journal of Medical Genetics|March 8, 2024

Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insightsBurcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.

BMC Neurology|October 26, 2011

Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case reportConceição Bettencourt, Cristina Santos, Paula Coutinho, et al.

The Journal of Biological Chemistry|May 30, 2006

Biorxiv : the Preprint Server for Biology|February 20, 2025

DNA methylation as a contributor to dysregulation of <i>STX6</i> and other frontotemporal lobar degeneration genetic risk-associated lociNaiomi Rambarack, Katherine Fodder, Megha Murthy, et al.

Human Genetics|July 2, 2014

Population and genomic lessons from genetic analysis of two Indian populationsGarima Juyal, Mayukh Mondal, Pierre Luisi, et al.

Acta Neuropathologica Communications|July 5, 2025

DNA methylation as a contributor to dysregulation of STX6 and other frontotemporal Lobar degeneration genetic risk-associated lociNaiomi Rambarack, Katherine Fodder, Megha Murthy, et al.