Marcus Naymik - Concepedia

Author

Marcus Naymik

Translational Genomics Research Institute

Also Known As

M. A. Naymik, M. Naymik, M.A. Naymik, Marcus A Naymik, Marcus A. Naymik, Marcus Naymik, Naymik, Marcus, Naymik, Marcus A.

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Translational Genomics Research Institute University of Southern California Arizona State University Baylor Genetics Baylor College of Medicine

About

Marcus Naymik is an author at Translational Genomics Research Institute specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	847
2	Arts	1	1	48
3	Health Sciences	1	1	50
4	Social Sciences	1	1	26
5	Cognitive Science	1	1	50

Marcus Naymik

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Resistance to autosomal dominant Alzheimer’s disease in an APOE3 Christchurch homozygote: a case report Joseph F. Arboleda‐Velásquez, Francisco Lopera, Michael O’Hare, Nature Medicine Neurodegenerative DiseasesAlzheimer's DiseaseGeneticsDegenerative PathologyNeuroscience	2019	559
Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases Francisco M. De La Vega, Shimul Chowdhury, Barry Moore, Genome Medicine	2021	135
Maternal choline supplementation ameliorates Alzheimer’s disease pathology by reducing brain homocysteine levels across multiple generations Ramón Velázquez, Eric Ferreira, Wendy Winslow, Molecular Psychiatry Brain Homocysteine LevelsNeurodegenerative DiseasesAlzheimer's DiseaseMultiple GenerationsMaternal Choline Supplementation	2019	89
Transcriptome response of human skeletal muscle to divergent exercise stimuli Jared M. Dickinson, Andrew C. D’Lugos, Marcus Naymik, Journal of Applied Physiology	2018	85
Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation Chris Balak, Marianne Bénard, Élise Schaefer, The American Journal of Human Genetics Rna DysregulationAllelic VariantGenetic DisorderMedicineGenetics	2019	84
DNA Methylation and Expression Profiles of Whole Blood in Parkinson’s Disease Adrienne Henderson, Qi Wang, Bessie Meechoovet, Frontiers in Genetics	2021	78
Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish Aleksandra Siekierska, Hannah Stamberger, Tine Deconinck, Nature Communications	2019	50
Family history of Alzheimer’s disease alters cognition and is modified by medical and genetic factors Joshua S. Talboom, Asta K. Håberg, Matthew De Both, eLife First-degree Family HistoryGeriatric PsychiatryAgingGenetic FactorsAlzheimer ’	2019	50
De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness Isabelle Schrauwen, Elina Kari, Jacob Mattox, Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiology	2018	48
Family SES Is Associated with the Gut Microbiome in Infants and Children Candace R. Lewis, Kevin S. Bonham, Shelley McCann, Microorganisms	2021	35

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