Although family and twin studies show that there is a genetic component to migraine, no
genes predisposing to common forms of the disorder have been identified. The most …

Migraine is a debilitating neurological disorder affecting around one in seven people worldwide,
but its molecular mechanisms remain poorly understood. There is some debate about …

Migraine is the most common brain disorder, affecting approximately 14% of the adult
population, but its molecular mechanisms are poorly understood. We report the results of a meta-…

Migraine without aura is the most common form of migraine, characterized by recurrent
disabling headache and associated autonomic symptoms. To identify common genetic variants …

<p id="p001">This report identifies human skeletal diseases associated with mutations in <italic>WNT1</italic>.
In 10 family members with dominantly inherited, early-onset osteoporosis…

Migraine affects over a billion individuals worldwide but its genetic underpinning remains
largely unknown. Here, we performed a genome-wide association study of 102,084 migraine …

… Author links open overlay panel Verneri Anttila 1 , Maija Wessman 2 , Mikko Kallela 3 , … a
large-scale family study reported a locus on 4q24 (Wessman et al., 2002). This was followed by …

Hematopoietic stem cells (HSCs) are characterized by their dual abilities to undergo
differentiation into multiple hematopoietic cell lineages or to undergo self-renewal. The molecular …

Food neophobia refers to reluctance to eat unfamiliar foods. We determined the heritability
of food neophobia in a family and a twin sample. The family sample consisted of 28 Finnish …

… Body mass index (in kg/m 2 ) ranged from 15.3 to 42.0 (x̄ ± SD: 26.0 ± 4.6). The study
protocol was approved by the Ethical Committee of Helsinki University Central Hospital. All …