Ludmila Pawlikowska, Ph.D.
Affiliations: | 2002 | University of California, San Francisco, San Francisco, CA |
Area:
GeneticsGoogle:
"Ludmila Pawlikowska"Parents
Sign in to add mentor| Nigel Killeen | grad student | 2002 | UCSF | |
| (A mouse model of human liver disease due to inherited mutations in the ATP8B1 (FIC1) gene.) | ||||
| Pui Kwok | post-doc | UCSF (GenetiTree) | ||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Pawlikowska L, Nelson J, Guo DE, et al. (2018) Association of common candidate variants with vascular malformations and intracranial hemorrhage in hereditary hemorrhagic telangiectasia. Molecular Genetics & Genomic Medicine. 6: 350-356 |
| LaHue SC, Kim H, Pawlikowska L, et al. (2018) Frequency and characteristics associated with inherited thrombophilia in patients with intracranial dural arteriovenous fistula. Journal of Neurosurgery. 1-5 |
| Nelson J, Bendjilali N, Weinsheimer SM, et al. (2018) Abstract WP426: Does Intracerebral Hemorrhage in Brain Arteriovenous Malformation Share Genetic Risk Factors With Primary Intracerebral Hemorrhage? Stroke. 49 |
| Weinsheimer S, Bendjilali N, Nelson J, et al. (2016) Genome-wide association study of sporadic brain arteriovenous malformations. Journal of Neurology, Neurosurgery, and Psychiatry |
| Choquet H, Trapani E, Goitre L, et al. (2016) Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1. Free Radical Biology & Medicine. 92: 100-109 |
| Tranah GJ, Yaffe K, Katzman SM, et al. (2015) Mitochondrial DNA Heteroplasmy Associations With Neurosensory and Mobility Function in Elderly Adults. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences |
| Pawlikowska L, Nelson J, Guo DE, et al. (2015) The 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. American Journal of Medical Genetics. Part A. 167: 1262-7 |
| Kremer PH, Koeleman BP, Pawlikowska L, et al. (2015) Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 524-9 |
| Choquet H, Pawlikowska L, Nelson J, et al. (2014) Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity. Cerebrovascular Diseases (Basel, Switzerland). 38: 433-40 |
| Hackett CS, Quigley DA, Wong RA, et al. (2014) Expression quantitative trait loci and receptor pharmacology implicate Arg1 and the GABA-A receptor as therapeutic targets in neuroblastoma. Cell Reports. 9: 1034-46 |