Researcher profile · Semantic Scholar

Nadine Kraemer

h-index: 13
Works: 30
Citations: 631

Most-cited papers

Many roads lead to primary autosomal recessive microcephaly.
A. Kaindl, S. Passemard, Pavan Kumar, Nadine Kraemer +6 more
2010Progress in neurobiology217 citations
Semantic Scholar
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
Heba Farag, S. Froehler, K. Oexle, Ethiraj Ravindran +6 more
2013Orphanet Journal of Rare Diseases43 citations Open access
Semantic Scholar
Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation
L. Issa, Katrin Mueller, K. Seufert, Nadine Kraemer +5 more
2013Orphanet Journal of Rare Diseases42 citations Open access
Semantic Scholar
CDK5RAP2 expression during murine and human brain development correlates with pathology in primary autosomal recessive microcephaly.
L. Issa, Nadine Kraemer, C. Rickert, M. Sifringer +3 more
2013Cerebral Cortex40 citations Open access
Semantic Scholar
What’s the hype about CDK5RAP2?
Nadine Kraemer, L. Issa, Stefanie Hauck, S. Mani +2 more
2011Cellular and Molecular Life Sciences40 citations Open access
Semantic Scholar
Mutations in PTRH2 cause novel infantile-onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weakness
Hao Hu, Michelle L. Matter, Lina Issa-Jahns, M. Jijiwa +17 more
2014Annals of Clinical and Translational Neurology39 citations Open access
Semantic Scholar
Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation
Ethiraj Ravindran, Hao Hu, S. Yuzwa, L. R. Hernandez-Miranda +13 more
2017PLoS Genetics26 citations Open access
Semantic Scholar
bHLH gene expression in the Emx2-deficient dentate gyrus reveals defective granule cells and absence of migrating precursors.
J. Oldekamp, Nadine Kraemer, Gonzalo Alvarez-Bolado, T. Skutella
2004Cerebral Cortex25 citations
Semantic Scholar
Phenotype variability of infantile-onset multisystem neurologic, endocrine, and pancreatic disease IMNEPD
Sylvie Picker-Minh, C. Mignot, D. Doummar, M. Hashem +7 more
2016Orphanet Journal of Rare Diseases21 citations Open access
Semantic Scholar
A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing
Tao Chen, Bin Zhang, Thomas Ziegenhals, A. Prusty +10 more
2019PLoS Genetics19 citations Open access
Semantic Scholar
Reference genes in the developing murine brain and in differentiating embryonic stem cells
Nadine Kraemer, G. Neubert, L. Issa, O. Ninnemann +2 more
2012Neurological Research19 citations
Semantic Scholar
Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytes
Nadine Kraemer, Ethiraj Ravindran, S. Zaqout, G. Neubert +5 more
2015Cell Cycle18 citations Open access
Semantic Scholar
Altered inhibition and excitation in neocortical circuits in congenital microcephaly.
S. Zaqout, Kathrin Blaesius, Yuan-Ju Wu, Stefanie Ott +6 more
2019Neurobiology of Disease13 citations Open access
Semantic Scholar
Emx2 in the developing hippocampal fissure region
Tian-Yu Zhao, Nadine Kraemer, J. Oldekamp, Murat Çankaya +4 more
2006European Journal of Neuroscience13 citations Open access
Semantic Scholar
Pontine Tegmental Cap Dysplasia in an Extremely Preterm Infant and Review of the Literature
Sylvie Picker-Minh, S. Hartenstein, H. Proquitté, Sebastian Fröhler +9 more
2017Journal of Child Neurology10 citations
Semantic Scholar
Adding another dimension: Temporal development of the spatial distribution of soil and crop properties in slow-forming terrace systems
Nadine Kraemer, G. Dercon, P. Cisneros, Felipe Arango Lopez +1 more
2019Agriculture, Ecosystems & Environment9 citations Open access
Semantic Scholar
Previously reported new type of autosomal recessive primary microcephaly is caused by compound heterozygous ASPM gene mutations
Hao Hu, Vanessa Suckow, L. Musante, V. Roggenkamp +5 more
2014Cell Cycle8 citations Open access
Semantic Scholar
Novel Alternative Splice Variants of Mouse Cdk5rap2
Nadine Kraemer, Lina Issa-Jahns, G. Neubert, Ethiraj Ravindran +3 more
2015PLoS ONE7 citations Open access
Semantic Scholar
Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability
Ethiraj Ravindran, Cynthia Gutierrez de Velazco, Ali Ghazanfar, Nadine Kraemer +9 more
2021Journal of Medical Genetics6 citations Open access
Semantic Scholar
Genetic causes of MCPH in consanguineous Pakistani families
Nadine Kraemer, Sylvie Picker-Minh, A. A. Abbasi, Sebastian Fröhler +5 more
2016Clinical Genetics6 citations Open access
Semantic Scholar
Togaram1 is expressed in the neural tube and its absence causes neural tube closure defects
Yanyan Wang, Nadine Kraemer, Joanna Schneider, O. Ninnemann +7 more
2024HGG advances5 citations Open access
Semantic Scholar
PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD Patients
Sylvie Picker-Minh, Ilaria Luperi, Ethiraj Ravindran, Nadine Kraemer +6 more
2022Cerebellum3 citations Open access
Semantic Scholar
Proteome changes in autosomal recessive primary microcephaly
Sami Zaqout, A. Mannaa, Oliver Klein, Angelika Krajewski +8 more
2022Annals of Human Genetics2 citations Open access
Semantic Scholar
Induction of innate immune response in fresh human lung tissue ex vivo following P. aeruginosa infection
L. Mueller, Nadine Kraemer, P. Braubach, D. Jonigk +6 more
2018Cystic fibrosis1 citations
Semantic Scholar
P 306. Role of Cdk5rap2 in Neocortical Development
S. Zaqout, L. Becker, Nadine Kraemer, A. Kaindl
2018Neuropediatrics0 citations
Semantic Scholar
A New Form of a Mitochondriopathy
B. Hartmann, Hao Hu, Nadine Kraemer, L. Musante +5 more
20140 citations
Semantic Scholar
Modeling the MCPH phenotype: neural differentiation of Cdk5rap2-depleted murine embryonic stem cells affects proliferation and neural differentiation
Nadine Kraemer, Lina Issa-Jahns, Ethiraj Ravindran, G. Neubert +3 more
20140 citations
Semantic Scholar
Immunodeficiency, Centromeric Instability, Facial Anomalies Syndrome Type 2 (ICF2): Combined Immunodeficiency, Autoimmune Phenomena, and Intellectual Disability
Ethiraj Ravindran, Hang Du, Sebastian Fröhler, K. Strehl +9 more
20140 citations
Semantic Scholar
Cdk5rap2 knockdown in murine embryonic stem cells affects proliferation and neural differentiation, but not non-neural differentiation into beating cardiomyocytes
Nadine Kraemer, L. Issa, G. Neubert, A. Seiler +3 more
20140 citations
Semantic Scholar
A Novel Phenotype: Microcephaly, Intellectual Disability, and Mid-hindbrain Defect
Ethiraj Ravindran, Hao Hu, Nadine Kraemer, O. Ninnemann +7 more
20140 citations
Semantic Scholar

D. Schindler

×6

Hao Hu×6

L. Musante×5

H. Ropers×5

T. Wienker×5

C. Hübner×5

G. Neubert×5

S. Zaqout×5