P. Ylikotila

发表

Obesity and the Risk of Cryptogenic Ischemic Stroke in Young Adults.

Ana Catarina Fonseca, D. Jatužis, J. Sinisalo, 2022, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.

Mohamad Saad, Peter Holmans, Nicholas W Wood, 2013, Human molecular genetics.

Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

M. Pirinen, P. Donnelly, C. Spencer, 2012 .

Rivaroxaban versus aspirin for secondary prevention of ischaemic stroke in patients with cancer: a subgroup analysis of the NAVIGATE ESUS randomized trial

A. Demchuk, E. Themeles, Á. Chamorro, 2020, European journal of neurology.

Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study

D. Hernandez, M. Nalls, A. Singleton, 2017, Neurobiology of Aging.

Finnish Parkinson’s disease study integrating protein-protein interaction network data with exome sequencing analysis

D. Hernandez, M. Nalls, A. Singleton, 2019, Scientific Reports.

Corrigendum to Using genome-wide complex trait analysis to quantify 'missing heritability' in parkinson's disease [Human Molecular Genetics, 21: 22 (2012) 4996-5009] doi: 10.1093/hmg/dds335]

D. Hernandez, M. Nalls, A. Singleton, 2013 .

Genetic risk factors in Finnish patients with Parkinson's disease.

M. Nalls, A. Singleton, H. Soininen, 2017, Parkinsonism & related disorders.

Early pregnancy cerebral venous thrombosis and status epilepticus treated with levetiracetam and lacosamide throughout pregnancy.

P. Ylikotila, J. Ruuskanen, R. Ketola, 2015, Reproductive toxicology.

Brain white matter hyperintensities in Kawasaki disease: A case–control study

J. Hirvonen, R. Parkkola, J. Rinne, 2022, Frontiers in Neuroscience.

Global Impact of the COVID-19 Pandemic on Stroke Volumes and Cerebrovascular Events

Murali K. Kolikonda, C. Nolte, M. Reiser, 2022, Neurology.

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

Sonja W. Scholz, D. Hernandez, M. Nalls, 2019, The Lancet Neurology.

Diagnostic yield of emergency MRI in non-traumatic headache

H. Merisaari, P. Ylikotila, M. Nyman, 2022, Neuroradiology.

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinsons disease (vol 22, pg 1696, 2013)

Mohamad Saad, Nicholas W. Wood, Gibbs, 2013 .

Epidemiology of early-onset Parkinson's disease in Finland.

K. Majamaa, P. Ylikotila, R. Marttila, 2015, Parkinsonism & related disorders.

Association between Migraine and Cryptogenic Ischemic Stroke in Young Adults

Ana Catarina Fonseca, P. Jäkälä, Bettina von Sarnowski, 2020, Annals of neurology.

Variations of mitochondrial DNA polymerase γ in patients with Parkinson’s disease

S. Finnilä, K. Majamaa, J. Autere, 2013, Journal of Neurology.

Outcomes with Endovascular Treatment of Patients with M2 Segment MCA Occlusion in the Late Time Window

G. Pracucci, P. Ylikotila, D. Toni, 2023, American Journal of Neuroradiology.

Rivaroxaban or aspirin for patent foramen ovale and embolic stroke of undetermined source: a prespecified subgroup analysis from the NAVIGATE ESUS trial.

D. Tanné, D. Blacker, S. Connolly, 2018, The Lancet. Neurology.

24-hour ambulatory blood pressure and cryptogenic ischemic stroke in young adults

J. Sinisalo, P. Jäkälä, J. Putaala, 2023, Annals of medicine.

Searching for Explanations for Cryptogenic Stroke in the Young: Revealing the Triggers, Causes, and Outcome (SECRETO): Rationale and design

J. Ferro, C. Enzinger, F. de Leeuw, 2017, European stroke journal.

Genome Wide Assessment of Young Onset Parkinson’s Disease from Finland

D. Hernandez, M. Nalls, A. Singleton, 2012, PloS one.

Association of biallelic RFC1 expansion with early‐onset Parkinson's disease

N. Matsumoto, K. Majamaa, P. Ylikotila, 2023, European journal of neurology.

Imaging Outcomes of Emergency MRI in Patients with Suspected Cerebral Venous Sinus Thrombosis: A Retrospective Cohort Study

P. Ylikotila, V. Kytö, M. Nyman, 2023, Diagnostics.

Variants p.Q1236H and p.E1143G in mitochondrial DNA polymerase gamma POLG1 are not associated with increased risk for valproate‐induced hepatotoxicity or pancreatic toxicity: A retrospective cohort study of patients with epilepsy

L. Haataja, K. Majamaa, P. Myllynen, 2018, Epilepsia.

Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study

D. Hernandez, M. Nalls, A. Singleton, 2017, Neurobiology of Aging.

Incidence and outcome of perforations during medium vessel occlusion compared with large vessel occlusion thrombectomy

K. Fargen, C. Nolte, S. Wolfe, 2023, Journal of neurointerventional surgery.

Association between heavy alcohol consumption and cryptogenic ischaemic stroke in young adults: a case–control study

D. Jatužis, J. Sinisalo, T. Tatlisumak, 2024, Journal of neurology, neurosurgery, and psychiatry.

Periodontitis, Dental Procedures, and Young-Onset Cryptogenic Stroke

J. Sinisalo, N. Martinez-Majander, P. Ylikotila, 2024, Journal of dental research.

Global Impact of the COVID-19 Pandemic on Stroke Volumes and Cerebrovascular Events

Murali K. Kolikonda, C. Nolte, M. Reiser, 2023, Neurology.