Anu Kemppinen

Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene

Eveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen et al. · The American Journal of Human Genetics · 2010 · 240 citations · Full text

Genome-wide Association Study, Disease Susceptibility, Medicine +11

Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome

Sophie Winder‐Rhodes, Pablo Garcia-Reitboeck, Maria Ban et al. · Movement Disorders · 2011 · 83 citations

Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in Germany

Anke Tönjes, Eleftheria Zeggini, Péter Kovács et al. · European Journal of Human Genetics · 2009 · 79 citations · Full text

Obesity, Metabolic Syndrome, Body Composition +13

MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

Christina M. Lill, Brit‐Maren M. Schjeide, Christiane Graetz et al. · Brain · 2013 · 69 citations · Full text

Neurogenomics, Neurological Disorder, Genetics +24

A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis

Inger‐Lise Mero, Åslaug Rudjord Lorentzen, Maria Ban et al. · European Journal of Human Genetics · 2009 · 67 citations · Full text

Rare Diseases, Autoimmune Disease, Neurological Disorder +12