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in Mol Autism

Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism

H.G. Kim et al.
in Front Neurol

Linkage evidence for a two-locus inheritance of LQT-associated seizures in a multigenerational LQT family with a novel KCNQ1 loss-of-function mutation

H. Prüss et al.
in J Allergy Clin Immunol

Eleven loci with new reproducible genetic associations with allergic disease risk

M.A. Ferreira et al.
in J Allergy Clin Immunol

Evaluation of food allergy candidate loci in the Genetics of Food Allergy Study

I. Marenholz et al.
in J Invest Dermatol

SMARCAD1 haploinsufficiency underlies Huriez syndrome and associated skin cancer susceptibility

C. Günther et al.
in J Allergy Clin Immunol

A Canadian genome-wide association study and meta-analysis confirm HLA as a risk factor for peanut allergy independent of asthma

Y. Asai et al.
in Nat Genet

Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

M.A. Ferreira et al.
in Nat Commun

Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy

I. Marenholz et al.
in Genome Biol

Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy

M. Heinig et al.
in JAMA Otolaryngol Head Neck Surg

Association of TMTC2 with human nonsyndromic sensorineural hearing loss

C.L. Runge et al.