Shantel M. Weinsheimer, Ph.D.

Affiliations: 
2006 Wayne State University, Detroit, MI, United States 
Area:
Genetics, Molecular Biology
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"Shantel Weinsheimer"

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Gerard Tromp grad student 2006 Wayne State
 (Identification of positional and functional candidate genes in intracranial aneurysm.)
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Publications

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Weinsheimer SM, Alexander MD, Nelson J, et al. (2021) Abstract P42: Genetic Variants Associated With Vasospasm Following Aneurysmal Subarachnoid Hemorrhage Stroke. 52
Starnawska A, Hansen C, Sparsø T, et al. (2019) Differential Dna Methylation At Birth Associated With Mental Disorder In Individuals With 22Q11.2 Deletion Syndrome European Neuropsychopharmacology. 29
Weinsheimer S, Starnawska A, Hansen C, et al. (2019) Genome-Wide Methylomic Analysis Of Neonatal Blood From Danish Twins Discordant For Mental Illness European Neuropsychopharmacology. 29
Wray NR, Ripke S, Mattheisen M, et al. (2018) Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics
Nelson J, Bendjilali N, Weinsheimer SM, et al. (2018) Abstract WP426: Does Intracerebral Hemorrhage in Brain Arteriovenous Malformation Share Genetic Risk Factors With Primary Intracerebral Hemorrhage? Stroke. 49
Starnawska A, Hansen CS, Sparsø T, et al. (2017) Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome. Translational Psychiatry. 7
Weinsheimer S, Bendjilali N, Nelson J, et al. (2016) Genome-wide association study of sporadic brain arteriovenous malformations. Journal of Neurology, Neurosurgery, and Psychiatry
Kremer PH, Koeleman BP, Pawlikowska L, et al. (2015) Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 524-9
Tromp G, Weinsheimer S, Ronkainen A, et al. (2014) Molecular basis and genetic predisposition to intracranial aneurysm. Annals of Medicine. 46: 597-606
Bendjilali N, Nelson J, Weinsheimer S, et al. (2014) Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms. Journal of Neurology, Neurosurgery, and Psychiatry. 85: 1280-3
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