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Andrew B Singleton

Showing results (271-280 of 397) with videos related to

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Science Signaling|February 24, 2026
Temporal proteomic and phosphoproteomic dynamics during neuronal differentiation in the reference iPSC line KOLF2.1JYing Hao, Ziyi Li, Erika Lara, et al.
NPJ Parkinson'S Disease|April 2, 2022
Multi-modality machine learning predicting Parkinson's diseaseMary B Makarious, Hampton L Leonard, Dan Vitale, et al.
Brain : a Journal of Neurology|October 21, 2017
Clinical, pathological and functional characterization of riboflavin-responsive neuropathyAndreea Manole, Zane Jaunmuktane, Iain Hargreaves, et al.
Neurobiology of Aging|March 17, 2018
Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3Celeste Sassi, Michael A Nalls, Perry G Ridge, et al.
Neurobiology of Aging|September 6, 2016
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositisQiang Gang, Conceição Bettencourt, Pedro M Machado, et al.
Human Molecular Genetics|August 16, 2012
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseMargaux F Keller, Mohamad Saad, Jose Bras, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
CNV-Finder: Streamlining Copy Number Variation DiscoveryNicole Kuznetsov, Kensuke Daida, Mary B Makarious, et al.
Human Molecular Genetics|December 11, 2012
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's diseasePeter Holmans, Valentina Moskvina, Lesley Jones, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
JAMA Neurology|June 7, 2017
Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune DiseasesAree Witoelar, Iris E Jansen, Yunpeng Wang, et al.
Pageof 40

Showing results (271-280 of 397) with videos related to

Sort By:
Pageof 40
Science Signaling|February 24, 2026
Temporal proteomic and phosphoproteomic dynamics during neuronal differentiation in the reference iPSC line KOLF2.1JYing Hao, Ziyi Li, Erika Lara, et al.
NPJ Parkinson'S Disease|April 2, 2022
Multi-modality machine learning predicting Parkinson's diseaseMary B Makarious, Hampton L Leonard, Dan Vitale, et al.
Brain : a Journal of Neurology|October 21, 2017
Clinical, pathological and functional characterization of riboflavin-responsive neuropathyAndreea Manole, Zane Jaunmuktane, Iain Hargreaves, et al.
Neurobiology of Aging|March 17, 2018
Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3Celeste Sassi, Michael A Nalls, Perry G Ridge, et al.
Neurobiology of Aging|September 6, 2016
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositisQiang Gang, Conceição Bettencourt, Pedro M Machado, et al.
Human Molecular Genetics|August 16, 2012
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseMargaux F Keller, Mohamad Saad, Jose Bras, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
CNV-Finder: Streamlining Copy Number Variation DiscoveryNicole Kuznetsov, Kensuke Daida, Mary B Makarious, et al.
Human Molecular Genetics|December 11, 2012
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's diseasePeter Holmans, Valentina Moskvina, Lesley Jones, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
JAMA Neurology|June 7, 2017
Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune DiseasesAree Witoelar, Iris E Jansen, Yunpeng Wang, et al.
Pageof 40