Malin Melin

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

Christoph Klein, Magda Grudzien, Giridharan Appaswamy et al. · Nature Genetics · 2006 · 504 citations

Life Sciences, Genetics, Molecular Genetics +10

Mammary Tumor Development in Dogs Is Associated with <i>BRCA1</i> and <i>BRCA2</i>

Patricio Rivera, Malin Melin, Tara Biagi et al. · Cancer Research · 2009 · 150 citations

Medicine, Genetics, Molecular Genetics +17

Constitutional Downregulation of &lt;i&gt;SEMA5A&lt;/i&gt; Expression in Autism

Malin Melin, Birgit Carlsson, Henrik Anckarsäter et al. · Neuropsychobiology · 2006 · 96 citations · Full text

Life Sciences, Genetics, Molecular Biology +8

Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific <i>HAX1</i> mutations

Göran Carlsson, Ingrid van’t Hooft, Malin Melin et al. · Journal of Internal Medicine · 2008 · 83 citations · Full text

Medicine, Genetics, Neurology +17

Genome-Wide Association Study of Golden Retrievers Identifies Germ-Line Risk Factors Predisposing to Mast Cell Tumours

Maja L. Arendt, Malin Melin, Noriko Tonomura et al. · PLoS Genetics · 2015 · 57 citations · Full text

Life Sciences, Genetics, Oncology +17