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Author Details

Ludmila Pawlikowska
Center for Cerebrovascular Research
1996
81
36
PMIDPaper TitleJournal TitlePublished Year
34214981Somatic mosaicism in the MAPK pathway in sporadic brain arteriovenous malformation and association with phenotype.J Neurosurg2021
34214981Somatic mosaicism in the MAPK pathway in sporadic brain arteriovenous malformation and association with phenotype.J Neurosurg2021
34185176Cyclo-oxygenase 2, a putative mediator of vessel remodeling, is expressed in the brain AVM vessels and associates with inflammation.Acta Neurochir (Wien)2021
34389651Seizure Incidence Rates in Children and Adults With Familial Cerebral Cavernous Malformations.Neurology2021
34491620Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation.Mol Genet Genomic Med2021
34479577Pilot investigation of circulating angiogenic and inflammatory biomarkers associated with vascular malformations.Orphanet J Rare Dis2021
34491620Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation.Mol Genet Genomic Med2021
34389651Seizure Incidence Rates in Children and Adults With Familial Cerebral Cavernous Malformations.Neurology2021
34479577Pilot investigation of circulating angiogenic and inflammatory biomarkers associated with vascular malformations.Orphanet J Rare Dis2021
34185176Cyclo-oxygenase 2, a putative mediator of vessel remodeling, is expressed in the brain AVM vessels and associates with inflammation.Acta Neurochir (Wien)2021
31797976Angiopoietin-2 predicts morbidity in adults with Fontan physiology.Sci Rep2019
31797976Angiopoietin-2 predicts morbidity in adults with Fontan physiology.Sci Rep2019
29761168Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile salt export protein deficiencies.Hepatol Commun2018
29932521Association of common candidate variants with vascular malformations and intracranial hemorrhage in hereditary hemorrhagic telangiectasia.Mol Genet Genomic Med2018
29624150Frequency and characteristics associated with inherited thrombophilia in patients with intracranial dural arteriovenous fistula.J Neurosurg2018
29761168Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile salt export protein deficiencies.Hepatol Commun2018
29932521Association of common candidate variants with vascular malformations and intracranial hemorrhage in hereditary hemorrhagic telangiectasia.Mol Genet Genomic Med2018
29624150Frequency and characteristics associated with inherited thrombophilia in patients with intracranial dural arteriovenous fistula.J Neurosurg2018
26818729Genome-wide association study of sporadic brain arteriovenous malformations.J Neurol Neurosurg Psychiatry2016
26795600Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1.Free Radic Biol Med2016
27215212Association of common genetic variation in the protein C pathway genes with clinical outcomes in acute respiratory distress syndrome.Crit Care2016
26818729Genome-wide association study of sporadic brain arteriovenous malformations.J Neurol Neurosurg Psychiatry2016
27215212Association of common genetic variation in the protein C pathway genes with clinical outcomes in acute respiratory distress syndrome.Crit Care2016
26795600Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1.Free Radic Biol Med2016
25053769Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain.J Neurol Neurosurg Psychiatry2015
25847705The ACVRL1 c.314-35A>G polymorphism is associated with organ vascular malformations in hereditary hemorrhagic telangiectasia patients with ENG mutations, but not in patients with ACVRL1 mutations.Am J Med Genet A2015
25708422Erratum to: plasma soluble thrombomodulin levels are associated with mortality in the acute respiratory distress syndrome.Intensive Care Med2015
25900426Genetics of cerebral cavernous malformations: current status and future prospects.J Neurosurg Sci2015
25643902Plasma soluble thrombomodulin levels are associated with mortality in the acute respiratory distress syndrome.Intensive Care Med2015
26328603Mitochondrial DNA Heteroplasmy Associations With Neurosensory and Mobility Function in Elderly Adults.J Gerontol A Biol Sci Med Sci2015
25053769Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain.J Neurol Neurosurg Psychiatry2015
26328603Mitochondrial DNA Heteroplasmy Associations With Neurosensory and Mobility Function in Elderly Adults.J Gerontol A Biol Sci Med Sci2015
25900426Genetics of cerebral cavernous malformations: current status and future prospects.J Neurosurg Sci2015
25847705The ACVRL1 c.314-35A>G polymorphism is associated with organ vascular malformations in hereditary hemorrhagic telangiectasia patients with ENG mutations, but not in patients with ACVRL1 mutations.Am J Med Genet A2015
25708422Erratum to: plasma soluble thrombomodulin levels are associated with mortality in the acute respiratory distress syndrome.Intensive Care Med2015
25643902Plasma soluble thrombomodulin levels are associated with mortality in the acute respiratory distress syndrome.Intensive Care Med2015
24401931Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation.Cerebrovasc Dis2014
25928712Severity score for hereditary hemorrhagic telangiectasia.Orphanet J Rare Dis2014
25437558Expression quantitative trait loci and receptor pharmacology implicate Arg1 and the GABA-A receptor as therapeutic targets in neuroblastoma.Cell Rep2014
25472749Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity.Cerebrovasc Dis2014
24401931Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation.Cerebrovasc Dis2014
24777168Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms.J Neurol Neurosurg Psychiatry2014
25928712Severity score for hereditary hemorrhagic telangiectasia.Orphanet J Rare Dis2014
25472749Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity.Cerebrovasc Dis2014
25437558Expression quantitative trait loci and receptor pharmacology implicate Arg1 and the GABA-A receptor as therapeutic targets in neuroblastoma.Cell Rep2014
24777168Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms.J Neurol Neurosurg Psychiatry2014
24098321A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation.PLoS One2013
24098321A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation.PLoS One2013
24323303Polymorphisms in ACVRL1 and endoglin genes are not associated with sporadic and HHT-related brain AVMs in Dutch patients.Transl Stroke Res2013
25221778Brain Vascular Malformation Consortium: Overview, Progress and Future Directions.J Rare Disord2013
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Collaborators

Pui-Yan Kwok
Cardiovascular Research Institute, University of California San Francisco
Co-authored papers 34
Nerissa U Ko
Department of Neurology University of California San Francisco CA.
Co-authored papers 7
Tamara B Harris
National Institute on Aging
Co-authored papers 7
Michael A Matthay
Cardiovascular Research Institute, University of California san francisco
Co-authored papers 7
Kathleen D Liu
University of California san francisco
Co-authored papers 6
Elad Ziv
Institute for Human Genetics, University of California San Francisco (UCSF)
Co-authored papers 6
Wen-Chi Hsueh
Co-authored papers 5
Nelson B Freimer
Co-authored papers 4
Hélène Choquet
Co-authored papers 4
Mary A Whooley
San Francisco Veterans Affairs Medical Center
Co-authored papers 4
Nick Patterson
Harvard University
Co-authored papers 4
Alexander P Reiner
Co-authored papers 4
Carolyn S Calfee
University of California San Francisco
Co-authored papers 4
Peter F Whitington
Ann and Robert H Lurie Children's Hospital of Chicago
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Nicholas J Schork
University of California San Diego
Co-authored papers 3
Esteban G Burchard
University of California San Francisco (UCSF)
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Arti Tandon
Co-authored papers 3
Mike A Nalls
Center for Alzheimer's and Related Dementias, National Institutes of Health
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Rongling Li
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
Gregory J Tranah
California Pacific Medical Center
Co-authored papers 3
Kiran K Khush
Co-authored papers 3
Yangfan Liu
Co-authored papers 2
Suzanne M Leal
Center for Statistical Genetics, Columbia University Medical Center
Co-authored papers 2
David A Hinds
23andMe Inc.
Co-authored papers 2
Albert V Smith
University of Michigan School of Public Health ann arbor
Co-authored papers 2
Jun Yu
Beijing Institute of Genomics, Chinese Academy of Sciences
Co-authored papers 2
Jessica Roy
Co-authored papers 2
Jian-Bing Fan
Nanfang Hospital and Basic Medical College, Southern Medical University
Co-authored papers 2
Jean-Fran??ois Olivier
McGill University Health Center
Co-authored papers 2
Robert W Plumb
Co-authored papers 2
Release 1.2