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Temporal associations of plasma levels of the secreted phospholipase A2 family and mortality in severe COVID‐19.
Published in:
European Journal of Immunology, 2024, v. 54, n. 6, p. 1, doi. 10.1002/eji.202350721
By:
- Lu, Eric;
- Hara, Aki;
- Sun, Shudong;
- Hallmark, Brian;
- Snider, Justin M.;
- Seeds, Michael C.;
- Watkins, Joseph C.;
- McCall, Charles E.;
- Zhang, Hao Helen;
- Yao, Guang;
- Chilton, Floyd H.
Publication type:
Article
The ratio of human X chromosome to autosome diversity is positively correlated with genetic distance from genes.
Published in:
Nature Genetics, 2010, v. 42, n. 10, p. 830, doi. 10.1038/ng.651
By:
- Hammer, Michael F.;
- Woerner, August E.;
- Mendez, Fernando L.;
- Watkins, Joseph C.;
- Cox, Murray P.;
- Wall, Jeffrey D.
Publication type:
Article
The International SCN8A Patient Registry: A Scientific Resource to Advance the Understanding and Treatment of a Rare Pediatric Neurodevelopmental Syndrome.
Published in:
Journal of Registry Management, 2023, v. 50, n. 1, p. 4
By:
- Andrews, Jennifer G.;
- Galindo, Maureen Kelly;
- Hack, Joshua B.;
- Watkins, Joseph C.;
- Conecker, Gabrielle A.;
- Hammer, Michael F.
Publication type:
Article
Genomic Evidence of Local Adaptation to Climate and Diet in Indigenous Siberians.
Published in:
Molecular Biology & Evolution, 2019, v. 36, n. 2, p. 315, doi. 10.1093/molbev/msy211
By:
- Hallmark, Brian;
- Karafet, Tatiana M;
- Hsieh, PingHsun;
- Osipova, Ludmila P;
- Watkins, Joseph C;
- Hammer, Michael F
Publication type:
Article
The Role of Phylogenetically Conserved Elements in Shaping Patterns of Human Genomic Diversity.
Published in:
Molecular Biology & Evolution, 2018, v. 35, n. 9, p. 2284, doi. 10.1093/molbev/msy145
By:
- Woerner, August E;
- Veeramah, Krishna R;
- Watkins, Joseph C;
- Hammer, Michael F
Publication type:
Article
Evidence for Increased Levels of Positive and Negative Selection on the X Chromosome versus Autosomes in Humans.
Published in:
Molecular Biology & Evolution, 2014, v. 31, n. 9, p. 2267, doi. 10.1093/molbev/msu166
By:
- Veeramah, Krishna R.;
- Gutenkunst, Ryan N.;
- Woerner, August E.;
- Watkins, Joseph C.;
- Hammer, Michael F.
Publication type:
Article
Neandertal Origin of Genetic Variation at the Cluster of OAS Immunity Genes.
Published in:
Molecular Biology & Evolution, 2013, v. 30, n. 4, p. 798, doi. 10.1093/molbev/mst004
By:
- Mendez, Fernando L.;
- Watkins, Joseph C.;
- Hammer, Michael F.
Publication type:
Article
Global Genetic Variation at OAS1 Provides Evidence of Archaic Admixture in Melanesian Populations.
Published in:
Molecular Biology & Evolution, 2012, v. 29, n. 6, p. 1513, doi. 10.1093/molbev/msr301
By:
- Mendez, Fernando L.;
- Watkins, Joseph C.;
- Hammer, Michael F.
Publication type:
Article
An Early Divergence of KhoeSan Ancestors from Those of Other Modern Humans Is Supported by an ABC-Based Analysis of Autosomal Resequencing Data.
Published in:
Molecular Biology & Evolution, 2012, v. 29, n. 2, p. 617, doi. 10.1093/molbev/msr212
By:
- Veeramah, Krishna R.;
- Wegmann, Daniel;
- Woerner, August;
- Mendez, Fernando L.;
- Watkins, Joseph C.;
- Destro-Bisol, Giovanni;
- Soodyall, Himla;
- Louie, Leslie;
- Hammer, Michael F.
Publication type:
Article
Evaluating IPMN and pancreatic carcinoma utilizing quantitative histopathology.
Published in:
Cancer Medicine, 2016, v. 5, n. 10, p. 2841, doi. 10.1002/cam4.923
By:
- Glazer, Evan S.;
- Zhang, Hao Helen;
- Hill, Kimberly A.;
- Patel, Charmi;
- Kha, Stephanie T.;
- Yozwiak, Michael L.;
- Bartels, Hubert;
- Nafissi, Nellie N.;
- Watkins, Joseph C.;
- Alberts, David S.;
- Krouse, Robert S.
Publication type:
Article
Variable patterns of mutation density among NaV1.1, NaV1.2 and NaV1.6 point to channel-specific functional differences associated with childhood epilepsy.
Published in:
PLoS ONE, 2020, v. 15, n. 8, p. 1, doi. 10.1371/journal.pone.0238121
By:
- Encinas, Alejandra C.;
- Watkins, Joseph C.;
- Longoria, Iris Arenas;
- Johnson, J. P.;
- Hammer, Michael F.
Publication type:
Article
Influence of age at seizure onset on the acquisition of neurodevelopmental skills in an SCN8A cohort.
Published in:
Epilepsia (Series 4), 2019, v. 60, n. 8, p. 1711, doi. 10.1111/epi.16288
By:
- Encinas, Alejandra C.;
- Moore, Ida (Ki) M.;
- Watkins, Joseph C.;
- Hammer, Michael F.
Publication type:
Article
Clinical implications of SCN1A missense and truncation variants in a large Japanese cohort with Dravet syndrome.
Published in:
Epilepsia (Series 4), 2017, v. 58, n. 2, p. 282, doi. 10.1111/epi.13639
By:
- Ishii, Atsushi;
- Watkins, Joseph C.;
- Chen, Debbie;
- Hirose, Shinichi;
- Hammer, Michael F.
Publication type:
Article
Identification of an Allele-Specific Transcription Factor Binding Interaction that May Regulate PLA2G2A Gene Expression.
Published in:
Bioinformatics & Biology Insights, 2024, p. 1, doi. 10.1177/11779322241261427
By:
- Hara, Aki;
- Lu, Eric;
- Johnstone, Laurel;
- Wei, Michelle;
- Sun, Shudong;
- Hallmark, Brian;
- Watkins, Joseph C;
- Zhang, Hao Helen;
- Yao, Guang;
- Chilton, Floyd H
Publication type:
Article
Balinese Y-Chromosome Perspective on the Peopling of Indonesia: Genetic Contributions from Pre-Neolithic Hunter- Gatherers, Austronesian Farmers, and Indian Traders.
Published in:
Human Biology, 2005, v. 77, n. 1, p. 93, doi. 10.1353/hub.2005.0030
By:
- Karafet, Tatiana M.;
- Lansing, J. S.;
- Redd, Alan J.;
- Reznikova, Svetlana;
- Watkins, Joseph C.;
- Surata, S. P. K.;
- Arthawiguna, W. A.;
- Mayer, Laura;
- Bamshad, Michael;
- Jorde, Lynn B.;
- Hammer, Michael F.
Publication type:
Article
Candesartan restores blood–brain barrier dysfunction, mitigates aberrant gene expression, and extends lifespan in a knockin mouse model of epileptogenesis.
Published in:
Clinical Science, 2024, v. 138, n. 17, p. 1089, doi. 10.1042/CS20240771
By:
- Hammer, Michael F.;
- Bahramnejad, Erfan;
- Watkins, Joseph C.;
- Ronaldson, Patrick T.
Publication type:
Article
Sex differences in physiological response to increased neuronal excitability in a knockin mouse model of pediatric epilepsy.
Published in:
Clinical Science, 2024, v. 138, n. 4, p. 205, doi. 10.1042/CS20231572
By:
- Hammer, Michael F.;
- Krzyzaniak, Collin T.;
- Bahramnejad, Erfan;
- Smelser, Kiran J.;
- Hack, Joshua B.;
- Watkins, Joseph C.;
- Ronaldson, Patrick T.
Publication type:
Article
Optimal Pair Matching Combined with Machine Learning Predicts a Significant Reduction in Myocardial Infarction Risk in African Americans Following Omega-3 Fatty Acid Supplementation.
Published in:
Nutrients, 2024, v. 16, n. 17, p. 2933, doi. 10.3390/nu16172933
By:
- Sun, Shudong;
- Hara, Aki;
- Johnstone, Laurel;
- Hallmark, Brian;
- Watkins, Joseph C.;
- Thomson, Cynthia A.;
- Schembre, Susan M.;
- Sergeant, Susan;
- Umans, Jason G.;
- Yao, Guang;
- Zhang, Hao Helen;
- Chilton, Floyd H.
Publication type:
Article

Found: 18

Temporal associations of plasma levels of the secreted phospholipase A<sub>2</sub> family and mortality in severe COVID‐19.

The ratio of human X chromosome to autosome diversity is positively correlated with genetic distance from genes.

The International SCN8A Patient Registry: A Scientific Resource to Advance the Understanding and Treatment of a Rare Pediatric Neurodevelopmental Syndrome.

Genomic Evidence of Local Adaptation to Climate and Diet in Indigenous Siberians.

The Role of Phylogenetically Conserved Elements in Shaping Patterns of Human Genomic Diversity.

Evidence for Increased Levels of Positive and Negative Selection on the X Chromosome versus Autosomes in Humans.

Neandertal Origin of Genetic Variation at the Cluster of OAS Immunity Genes.

Global Genetic Variation at OAS1 Provides Evidence of Archaic Admixture in Melanesian Populations.

An Early Divergence of KhoeSan Ancestors from Those of Other Modern Humans Is Supported by an ABC-Based Analysis of Autosomal Resequencing Data.

Evaluating IPMN and pancreatic carcinoma utilizing quantitative histopathology.

Variable patterns of mutation density among Na<sub>V</sub>1.1, Na<sub>V</sub>1.2 and Na<sub>V</sub>1.6 point to channel-specific functional differences associated with childhood epilepsy.

Influence of age at seizure onset on the acquisition of neurodevelopmental skills in an SCN8A cohort.

Clinical implications of SCN1A missense and truncation variants in a large Japanese cohort with Dravet syndrome.

Identification of an Allele-Specific Transcription Factor Binding Interaction that May Regulate PLA2G2A Gene Expression.

Balinese Y-Chromosome Perspective on the Peopling of Indonesia: Genetic Contributions from Pre-Neolithic Hunter- Gatherers, Austronesian Farmers, and Indian Traders.

Candesartan restores blood–brain barrier dysfunction, mitigates aberrant gene expression, and extends lifespan in a knockin mouse model of epileptogenesis.

Sex differences in physiological response to increased neuronal excitability in a knockin mouse model of pediatric epilepsy.

Optimal Pair Matching Combined with Machine Learning Predicts a Significant Reduction in Myocardial Infarction Risk in African Americans Following Omega-3 Fatty Acid Supplementation.