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Systems and Synthetic Biology
|
November 13, 2008
Modelling molecular interaction pathways using a two-stage identification algorithm
Padhraig Gormley, Kang Li, George W Irwin
Plos One
|
January 9, 2025
Patient stratification by genetic risk in Alzheimer's disease is only effective in the presence of phenotypic heterogeneity
Jack Euesden, Muhammad Ali, Chloe Robins, et al.
Genome Medicine
|
August 21, 2016
Migraine genetics: from genome-wide association studies to translational insights
Padhraig Gormley, Bendik S Winsvold, Dale R Nyholt, et al.
Neurology
|
October 12, 2021
Phenotypic and Genotypic Associations Between Migraine and Lipoprotein Subfractions
Yanjun Guo, Iyas Daghlas, Padhraig Gormley, et al.
Neurology. Genetics
|
February 7, 2022
Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement
Iyas Daghlas, Muralidharan Sargurupremraj, Rebecca Danning, et al.
Cephalalgia : an International Journal of Headache
|
October 14, 2021
Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families
Paavo Häppölä, Padhraig Gormley, Marjo E Nuottamo, et al.
EMBO Molecular Medicine
|
November 29, 2015
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy
Borislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
EMBO Molecular Medicine
|
December 3, 2017
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy
Borislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
Cephalalgia : an International Journal of Headache
|
March 1, 2018
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families
Marjo Eveliina Hiekkala, Pietari Vuola, Ville Artto, et al.
Plos One
|
September 29, 2017
Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants
Bendik S Winsvold, Francesco Bettella, Aree Witoelar, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 28) with videos related to
Sort By:
Page
of 3
Systems and Synthetic Biology
|
November 13, 2008
Modelling molecular interaction pathways using a two-stage identification algorithm
Padhraig Gormley, Kang Li, George W Irwin
Plos One
|
January 9, 2025
Patient stratification by genetic risk in Alzheimer's disease is only effective in the presence of phenotypic heterogeneity
Jack Euesden, Muhammad Ali, Chloe Robins, et al.
Genome Medicine
|
August 21, 2016
Migraine genetics: from genome-wide association studies to translational insights
Padhraig Gormley, Bendik S Winsvold, Dale R Nyholt, et al.
Neurology
|
October 12, 2021
Phenotypic and Genotypic Associations Between Migraine and Lipoprotein Subfractions
Yanjun Guo, Iyas Daghlas, Padhraig Gormley, et al.
Neurology. Genetics
|
February 7, 2022
Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement
Iyas Daghlas, Muralidharan Sargurupremraj, Rebecca Danning, et al.
Cephalalgia : an International Journal of Headache
|
October 14, 2021
Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families
Paavo Häppölä, Padhraig Gormley, Marjo E Nuottamo, et al.
EMBO Molecular Medicine
|
November 29, 2015
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy
Borislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
EMBO Molecular Medicine
|
December 3, 2017
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy
Borislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
Cephalalgia : an International Journal of Headache
|
March 1, 2018
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families
Marjo Eveliina Hiekkala, Pietari Vuola, Ville Artto, et al.
Plos One
|
September 29, 2017
Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants
Bendik S Winsvold, Francesco Bettella, Aree Witoelar, et al.
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of 3