Nadine Kraemer

Berlin, BE, Germany

Last Updated: 09/26/2026

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Found 21 publications

Togaram1 is expressed in the neural tube and its absence causes neural tube closure defects.

Togaram1 is expressed in the neural tube and its absence causes neural tube closure defects.

Journal: HGG advances

Published: May 10, 2024

PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD Patients.

PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD Patients.

Journal: Cerebellum (London, England)

Published: September 23, 2022

Proteome changes in autosomal recessive primary microcephaly.

Proteome changes in autosomal recessive primary microcephaly.

Journal: Annals of human genetics

Published: March 14, 2022

Comparison of the Minimally Invasive Tubular Transmuscular Approach with the Conventional Microsurgical Approach for Microsurgical Treatment of Lumbar Disk Herniation: A Prospective Randomized Study.

Comparison of the Minimally Invasive Tubular Transmuscular Approach with the Conventional Microsurgical Approach for Microsurgical Treatment of Lumbar Disk Herniation: A Prospective Randomized Study.

Journal: Journal of neurological surgery. Part A, Central European neurosurgery

Published: January 24, 2021

Zebrafish modeling mimics developmental phenotype of patients with RAPGEF1 mutation.

Zebrafish modeling mimics developmental phenotype of patients with RAPGEF1 mutation.

Journal: Clinical genetics

Published: December 24, 2020

Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability.

Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability.

Journal: Journal of medical genetics

Published: October 27, 2020

A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing.

A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing.

Journal: PLoS genetics

Published: March 05, 2019

Altered inhibition and excitation in neocortical circuits in congenital microcephaly.

Altered inhibition and excitation in neocortical circuits in congenital microcephaly.

Journal: Neurobiology of disease

Published: December 18, 2018

Pontine Tegmental Cap Dysplasia in an Extremely Preterm Infant and Review of the Literature.

Pontine Tegmental Cap Dysplasia in an Extremely Preterm Infant and Review of the Literature.

Journal: Journal of child neurology

Published: February 15, 2017

Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation.

Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation.

Journal: PLoS genetics

Published: June 23, 2016

CDK5RAP2 Is Required to Maintain the Germ Cell Pool during Embryonic Development.

CDK5RAP2 Is Required to Maintain the Germ Cell Pool during Embryonic Development.

Journal: Stem cell reports

Published: June 03, 2016

Phenotype variability of infantile-onset multisystem neurologic, endocrine, and pancreatic disease IMNEPD.

Phenotype variability of infantile-onset multisystem neurologic, endocrine, and pancreatic disease IMNEPD.

Journal: Orphanet journal of rare diseases

Published: March 02, 2016

Showing 1-12 of 21

Last Updated: 09/26/2026