Gregor Kuhlenbäumer

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

Daníel F. Guðbjartsson, Hilma Hólm, Sólveig Grétarsdóttir et al. · Nature Genetics · 2009 · 489 citations · Full text

Thrombosis, Ischemic Stroke, Cardiovascular Disease +11

Gut microbiota in Parkinson disease in a northern German cohort

Franziska Hopfner, Axel Künstner, Stefanie H. Müller et al. · Brain Research · 2017 · 326 citations

Probiotic, Dysbiosis, Microbiota +8

Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke

Sólveig Grétarsdóttir, Andrei Manolescu, Unnur Styrkársdóttir et al. · Annals of Neurology · 2008 · 285 citations

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

Gregor Kuhlenbäumer, Mark Hannibal, Eva Nelis et al. · Nature Genetics · 2005 · 259 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Molecular Neuroscience +8

De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

Arvid Suls, Johanna A. Jaehn, Angéla Kecskés et al. · The American Journal of Human Genetics · 2013 · 219 citations · Full text

Chd2 Cause, Dravet Syndrome, Molecular Neuroscience +8