Reis, André 1960-
André Reis deutscher Humangenetiker
VIAF ID: 40038313 ( Personal )
Permalink: http://viaf.org/viaf/40038313
Preferred Forms
- 100 0 _ ‡a André Reis ‡c deutscher Humangenetiker
- 100 1 _ ‡a Reis, André ‡d 1960-
- 100 1 _ ‡a Reis, André ‡d 1960-
4xx's: Alternate Name Forms (10)
5xx's: Related Names (3)
- 510 2 _ ‡a Deutsche Akademie der Naturforscher Leopoldina ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 551 _ _ ‡a Erlangen ‡4 ortw ‡4 https://d-nb.info/standards/elementset/gnd#placeOfActivity
- 551 _ _ ‡a Mainz ‡4 ortw ‡4 https://d-nb.info/standards/elementset/gnd#placeOfActivity
Works
Title | Sources |
---|---|
AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability | |
Analyse des Gens CLIP2 als Kandidatengen für mentale Retardierung | |
Analysis of gene CLIP2 as a candidate gene for mental retardation | |
Behavioral phenotype in five individuals with de novo mutations within the GRIN2B gene | |
clinical significance of small copy number variants in neurodevelopmental disorders | |
Clinical validation of genetic variants associated with in vitro chemotherapy-related lymphoblastoid cell toxicity | |
Common Genetic Determinants of Intraocular Pressure and Primary Open-Angle Glaucoma | |
Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis | |
Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum | |
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1 | |
Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma | |
Fragiles X-Chromosom bei Kindern mit Autistischem Syndrom | |
Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus | |
Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients | |
Identification and Characterization of New Genetic Risk Factors for Complex Diseases | |
Identification and characterization of the candidate genes FAR1, EDC3, FRRS1L and HMG20A in individuals with autosomal recessive intellectual disability | |
Identification of genes for autosomal recessive forms of mental retardation: mutation screening for the TUSC3-gene and homozygosity mapping to identify new gene loci | |
Identification of low-frequency TRAF3IP2 coding variants in psoriatic arthritis patients and functional characterization | |
Identifizierung und Charakterisierung genetischer Ursachen bei mentaler Retardierung | |
Identifizierung von Genen für autosomal rezessiv vererbte Intelligenzminderung | |
In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser Syndrome | |
MAN1B1 Mutation Leads to a Recognizable Phenotype: A Case Report and Future Prospects | |
Moleculargenetic Characterization of Constitutional Chromosomal Translocations for Positional Cloning of Disease-Causing Genes | |
Molekulargenetische Charakterisierung konstitutioneller chromosomaler Translokationen zur Positionsklonierung krankheitsverursachender Gene | |
Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopment | |
A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype | |
Null Mutation in PGAP1 Impairing Gpi-Anchor Maturation in Patients with Intellectual Disability and Encephalopathy | |
PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus | |
Rare Copy Number Variants Are a Common Cause of Short Stature | |
Slavic NBN Founder Mutation: A Role for Reproductive Fitness? | |
SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss | |
Tumor necrosis factor polymorphisms in psoriatic arthritis : association with the promoter polymorphism TNF-857 independent of the PSORS1 risk allele | |
Variants in RUNX3 contribute to susceptibility to psoriatic arthritis exhibiting further common ground with ankylosing spondylitis. |