About: Sonja Scholz

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) chercheuse (fr) investigadora (es) ഗവേഷക (ml) araştırmacı (tr) дослідниця (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl) researcher (en-ca) researcher (en-gb) researcher (en-us) hulumtuese (sq) ricercatrice (it) investigadora (ca) investigadora (gl) investigadora (pt) investigadora (ast)
rdfs:label	Sonja Scholz (en) Sonja Scholz (es) Sonja Scholz (fr) Sonja Scholz (it) Sonja Scholz (nl) Sonja Scholz (sl) Sonja Scholz (ast)
skos:prefLabel	Sonja Scholz (en) Sonja Scholz (es) Sonja Scholz (fr) Sonja Scholz (it) Sonja Scholz (nl) Sonja Scholz (sl) Sonja Scholz (ast)
name	Sonja Scholz (en) Sonja Scholz (es) Sonja Scholz (fr) Sonja Scholz (it) Sonja Scholz (nl) Sonja Scholz (sl) Sonja Scholz (ast)
Scopus author ID	wds:Q30362304-83AB8411-554B-44C7-A1EC-80660E44D9BD
Scopus author ID	12240193500
given name	wds:Q30362304-60F1ECB1-ED07-4D4F-8904-A97B4E6DC37E
given name	Sonja
instance of	wds:Q30362304-12A871B5-8496-4FA7-8271-6CA6DF382664
instance of	Homo sapiens
Loop ID	wds:Q30362304-ADADA4E9-8696-4E8F-9841-A00F96D6C7E3
Loop ID	625539
Semantic Scholar author ID	wds:Q30362304-6E9A808E-E564-4ECB-8327-1CDC192A89AE
Semantic Scholar author ID	34406349
skos:altLabel	S W Scholz (en) Scholz SW (en) Sonja W Scholz (en)
occupation	wds:Q30362304-CC9D7CD9-8CFE-4F83-8A2E-74CA22164CF4
employer	wds:Q30362304-07431B15-65F5-41E9-BA42-A155DDFB9763 wds:Q30362304-0F3FDC34-D8F0-49D0-BE20-6C3431560694 wds:Q30362304-8AAA5946-B296-46BB-BA7A-27966FB0A752 wds:Q30362304-E026F8CA-FE79-491B-B27D-A3D77F4AB935
sex or gender	wds:Q30362304-0FC30456-E2F8-49D9-902F-01E96CE6D553
occupation	researcher
employer	National Institute of Neurological Disorders and Stroke Georgetown University National Institute on Aging Johns Hopkins University
sex or gender	female organism
Springer Nature person ID	wds:Q30362304-272EAD99-A689-49D5-8554-675045AE5EE7
ORCID iD	wds:Q30362304-538F4980-112A-4218-9B82-F4117FBFC071
Dimensions author ID	wds:Q30362304-3EE4758D-2467-4F0C-8872-22A6BE2C8F90
ORCID iD	https://orcid.org/0000-0002-6623-0429
Springer Nature person ID	01015567610.50
ORCID iD	0000-0002-6623-0429
Dimensions author ID	01015567610.50
ResearcherID	wds:Q30362304-BC21512C-64CF-4354-9865-5594F2DF7E0E
Publons author ID	wds:Q30362304-9009c9c6-13a8-4f21-adc4-6407b7fd3d64
ResearcherID	R-5524-2017
Publons author ID	729754
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q30362304
is author of	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data Structural genomic variation in ischemic stroke A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD SNCA variants are associated with increased risk for multiple system atrophy Genomewide SNP assay reveals mutations underlying Parkinson disease Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals Genotype, haplotype and copy-number variation in worldwide human populations Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis Exome sequencing reveals VCP mutations as a cause of familial ALS Genome-wide association study reveals genetic risk underlying Parkinson's disease Multiple system atrophy as emerging template for accelerated drug discovery in α-synucleinopathies Genetic players in multiple system atrophy: unfolding the nature of the beast

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