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Publications by Dagmar Wieczorek
UBQLN4 Represses Homologous Recombination and Is Overexpressed in Aggressive Tumors
Cell
Biochemistry
Genetics
Molecular Biology
CEP152 Is a Genome Maintenance Protein Disrupted in Seckel Syndrome
Nature Genetics
Genetics
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
American Journal of Human Genetics
Genetics
De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders
American Journal of Human Genetics
Genetics
Neu-Laxova Syndrome Is a Heterogeneous Metabolic Disorder Caused by Defects in Enzymes of the L-Serine Biosynthesis Pathway
American Journal of Human Genetics
Genetics
De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A (PPP2CA) Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders
American Journal of Human Genetics
Genetics
Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Hematopoietic Stem Cell Transplantation in an Infant With Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome
Frontiers in Immunology
Allergy
Immunology
Platelet Defects in Congenital Variant of Rett Syndrome Patients With FOXG1 Mutations or Reduced Expression Due to a Position Effect at 14q12
European Journal of Human Genetics
Genetics
Genetic Predisposition in Children With Cancer – Affected Families' Acceptance of Trio-Wes
European Journal of Pediatrics
Child Health
Pediatrics
Perinatology
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