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Author Details

Mary Kusenda
Clinic for Cattle, University of Veterinary Medicine Hannover
2008
10
7
PMIDPaper TitleJournal TitlePublished Year
34134768Postoperative wound assessment in cattle: How reliable is the back hand palpation?Ir Vet J2021
34134768Postoperative wound assessment in cattle: How reliable is the back hand palpation?Ir Vet J2021
25614605The mammalian cervical vertebrae blueprint depends on the T (brachyury) gene.Genetics2015
25614605The mammalian cervical vertebrae blueprint depends on the T (brachyury) gene.Genetics2015
25862397Vertebral and spinal dysplasia: A novel dominantly inherited congenital defect in Holstein cattle.Vet J2015
26391891The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.J Child Neurol2015
26391891The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.J Child Neurol2015
25862397Vertebral and spinal dysplasia: A novel dominantly inherited congenital defect in Holstein cattle.Vet J2015
23194055Effects of dexamethasone-21-isonicotinate on peripheral insulin action in dairy cows 5 days after surgical correction of abomasal displacement.J Vet Intern Med2013
23194055Effects of dexamethasone-21-isonicotinate on peripheral insulin action in dairy cows 5 days after surgical correction of abomasal displacement.J Vet Intern Med2013
21924930Minimally-invasive catheterization of the portal, hepatic and cranial mesenteric veins and the abdominal aorta for quantitative determination of hepatic metabolism in dairy cows.Vet J2012
21924930Minimally-invasive catheterization of the portal, hepatic and cranial mesenteric veins and the abdominal aorta for quantitative determination of hepatic metabolism in dairy cows.Vet J2012
21448237Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.Eur J Hum Genet2011
21448237Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.Eur J Hum Genet2011
19855392Microduplications of 16p11.2 are associated with schizophrenia.Nat Genet2009
19855392Microduplications of 16p11.2 are associated with schizophrenia.Nat Genet2009
18369103Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.Science2008
19287137The role of rare structural variants in the genetics of autism spectrum disorders.Cytogenet Genome Res2008
18369103Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.Science2008
19287137The role of rare structural variants in the genetics of autism spectrum disorders.Cytogenet Genome Res2008
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Collaborators

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Co-authored papers 5
MS Research Unit
Co-authored papers 4
University of Washington
Co-authored papers 3
University of Washington
Co-authored papers 3
National Institute of Mental Health, National Institutes of Health
Co-authored papers 3
National Institute of Mental Health in Bethesda
Co-authored papers 3
University of Washington
Co-authored papers 3
Wellcome Sanger Institute
Co-authored papers 3
Co-authored papers 2
Center for Immunotherapy and Precision-Immuno-Oncology, Cleveland Clinic
Co-authored papers 2
Stanley Institute for Cognitive Genomics
Co-authored papers 2
Bharathidasan University, Indian Institute of Science
Co-authored papers 2
B.P. Koirala Institute of Health Sciences
Co-authored papers 2
UC Davis Center for Neuroscience.
Co-authored papers 2
Seattle Children's Research Institute
Co-authored papers 2
SUNY College at Old Westbury
Co-authored papers 2
Co-authored papers 2
Co-authored papers 1
University of Washington
Co-authored papers 1
Children's Hospital of Philadelphia
Co-authored papers 1
Co-authored papers 1
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Virginia Commonwealth University
Co-authored papers 1
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University of Washington
Co-authored papers 1
Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
Co-authored papers 1
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Uppsala University
Co-authored papers 1
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Central Institute of Mental Health, University of Mannheim
Co-authored papers 1