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Author/Creator Boncoraglio, Giorgio

1. Association of MTHFR C677T Genotype With Ischemic Stroke Is Confined to Cerebral Small Vessel Disease Subtype. Issue 3 (March 2016)

Authors:
Rutten-Jacobs, Loes C.A.; Traylor, Matthew; Adib-Samii, Poneh; Thijs, Vincent; Sudlow, Cathie; Rothwell, Peter M.; Boncoraglio, Giorgio; Dichgans, Martin; Meschia, James; Maguire, Jane; Levi, Christopher; Rost, Natalia S.; Rosand, Jonathan; Hassan, Ahamad; Bevan, Steve; Markus, Hugh S.
Journal:
Stroke
Issue:
Volume 47:Issue 3(2016)
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Record Type:
Journal Article
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3. Common NOTCH3 Variants and Cerebral Small-Vessel Disease. Issue 6 (June 2015)

Authors:
Rutten-Jacobs, Loes C.A.; Traylor, Matthew; Adib-Samii, Poneh; Thijs, Vincent; Sudlow, Cathie; Rothwell, Peter M.; Boncoraglio, Giorgio; Dichgans, Martin; Bevan, Steve; Meschia, James; Levi, Christopher; Rost, Natalia S.; Rosand, Jonathan; Hassan, Ahamad; Markus, Hugh S.
Journal:
Stroke
Issue:
Volume 46:Issue 6(2015)
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Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Common NOTCH3 Variants and Cerebral Small-Vessel Disease. Issue 6 (June 2015)

Authors:
Rutten-Jacobs, Loes C.A.; Traylor, Matthew; Adib-Samii, Poneh; Thijs, Vincent; Sudlow, Cathie; Rothwell, Peter M.; Boncoraglio, Giorgio; Dichgans, Martin; Bevan, Steve; Meschia, James; Levi, Christopher; Rost, Natalia S.; Rosand, Jonathan; Hassan, Ahamad; Markus, Hugh S.
Journal:
Stroke
Issue:
Volume 46:Issue 6(2015)
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Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Differences in Common Genetic Predisposition to Ischemic Stroke by Age and Sex. Issue 11 (November 2015)

Authors:
Traylor, Matthew; Rutten-Jacobs, Loes C.A.; Holliday, Elizabeth G.; Malik, Rainer; Sudlow, Cathie; Rothwell, Peter M.; Maguire, Jane M.; Koblar, Simon A.; Bevan, Steve; Boncoraglio, Giorgio; Dichgans, Martin; Levi, Chris; Lewis, Cathryn M.; Markus, Hugh S.
Journal:
Stroke
Issue:
Volume 46:Issue 11(2015)
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Record Type:
Journal Article
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6. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting. (29th January 2019)

Authors:
Chauhan, Ganesh; Adams, Hieab H.H.; Satizabal, Claudia L.; Bis, Joshua C.; Teumer, Alexander; Sargurupremraj, Muralidharan; Hofer, Edith; Trompet, Stella; Hilal, Saima; Smith, Albert Vernon; Jian, Xueqiu; Malik, Rainer; Traylor, Matthew; Pulit, Sara L.; Amouyel, Philippe; Mazoyer, Bernard; Zhu, Y...
Journal:
Neurology
Issue:
Volume 92:Number 5(2019)
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Record Type:
Journal Article
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7. Genetic Associations With White Matter Hyperintensities Confer Risk of Lacunar Stroke. Issue 5 (May 2016)

Authors:
Traylor, Matthew; Rutten-Jacobs, Loes C.A.; Thijs, Vincent; Holliday, Elizabeth G.; Levi, Chris; Bevan, Steve; Malik, Rainer; Boncoraglio, Giorgio; Sudlow, Cathie; Rothwell, Peter M.; Dichgans, Martin; Markus, Hugh S.
Journal:
Stroke
Issue:
Volume 47:Issue 5(2016)
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Record Type:
Journal Article
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8. Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11, 226). (19th February 2019)

Authors:
Traylor, Matthew; Tozer, Daniel J.; Croall, Iain D.; Lisiecka Ford, Danuta M.; Olorunda, Abiodun Olubunmi; Boncoraglio, Giorgio; Dichgans, Martin; Lemmens, Robin; Rosand, Jonathan; Rost, Natalia S.; Rothwell, Peter M.; Sudlow, Cathie L.M.; Thijs, Vincent; Rutten-Jacobs, Loes; Markus, Hugh S.
Journal:
Neurology
Issue:
Volume 92:Number 8(2019)
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Record Type:
Journal Article
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