Sonja W. Scholz - Concepedia

Author

Sonja W. Scholz

Also Known As

Ali Daneshmand, B Navi, Benatar, Michael, California Babak, Clifton L. Dalgard, Cristina Cereda, Danielle Posthuma, Dena G Hernandez, Dinara Sadykova, Erik Pioro

260

Publications

26K

Citations

H-Index

108

Concepts

All Affiliations

National Institute on Aging National Institutes of Health National Institute of Neurological Disorders and Stroke University College London Johns Hopkins University

About

Sonja W. Scholz is an author at National Institute on Aging specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	47	12.2K
2	Public Health	11	11	2.9K
3	Engineering	3	3	160
4	Natural Sciences	2	2	939
5	Social Sciences	2	2	424

Sonja W. Scholz

Publications

16.5K

Citations

H-Index

Page 1

	Year	Citations
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD Alan E. Renton, Elisa Majounie, Adrian J. Waite, Neuron ChromatinNeurodegenerative DiseasesAmyotrophic Lateral SclerosisGenetic DisorderGenetics	2011	4.4K
Genome-wide association study reveals genetic risk underlying Parkinson's disease Javier Simón‐Sánchez, Claudia Schulte, José Brás, Nature Genetics Genome-wide Association StudyGeneticsGenetic EpidemiologyGenetic FactorNeurodegeneration	2009	1.9K
Genotype, haplotype and copy-number variation in worldwide human populations Mattias Jakobsson, Sonja W. Scholz, Paul Scheet, Nature Haplotype DeterminationMolecular EcologyHuman VariationMedicineGenetics	2008	909
A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) David Melzer, John R. B. Perry, Dena Hernández, PLoS Genetics	2008	488
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture Ruth Chia, Marya S. Sabir, Sara Bandrés‐Ciga, Nature Genetics Neurodegenerative DiseasesAlzheimer's DiseaseGeneticsDementiaGenetic Architecture	2021	448
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data Hon‐Chung Fung, Sonja W. Scholz, Mar Matarín, The Lancet Neurology Neurodegenerative DiseasesFirst Stage AnalysisParkinson DiseaseGeneticsGenetic Epidemiology	2006	393
Detection of mosaic and population-level structural variants with Sniffles2 Moritz Smolka, Luis F. Paulin, Christopher M. Grochowski, Nature Biotechnology	2024	377
Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms Cornelis Blauwendraat, Karl Heilbron, Costanza L. Vallerga, Movement Disorders	2019	365
Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans Joyce van de Leemput, Jayanth Chandran, Melanie A. Knight, PLoS Genetics GeneticsMolecular GeneticsDisease Gene IdentificationItpr1 Underlies AtaxiaSocial Sciences	2007	342
<i>SNCA</i> variants are associated with increased risk for multiple system atrophy Sonja W. Scholz, Henry Houlden, Claudia Schulte, Annals of Neurology	2009	279

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