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Ludwig, Kerstin
One or more keywords matched the following items that are connected to
Ludwig, Kerstin
Item Type
Name
Academic Article
A post GWAS association study of SNPs associated with cleft lip with or without cleft palate in submucous cleft palate.
Academic Article
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.
Academic Article
Exome sequencing in large, multiplex bipolar disorder families from Cuba.
Academic Article
Deletions and loss-of-function variants in TP63 associated with orofacial clefting.
Academic Article
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients.
Academic Article
Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia.
Academic Article
'Location, Location, Location': a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palate.
Academic Article
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate.
Academic Article
Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population.
Academic Article
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome.
Academic Article
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.
Academic Article
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.
Academic Article
Genome-wide association study of alcohol dependence.
Academic Article
IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.
Academic Article
Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample.
Academic Article
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway.
Concept
Alleles
Academic Article
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality.
Academic Article
Allele-specific transcription factor binding in a cellular model of orofacial clefting.
Academic Article
Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations.
Search Criteria
Alleles
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