Year |
Citation |
Score |
2018 |
Pawlikowska L, Nelson J, Guo DE, McCulloch CE, Lawton MT, Kim H, Faughnan ME. Association of common candidate variants with vascular malformations and intracranial hemorrhage in hereditary hemorrhagic telangiectasia. Molecular Genetics & Genomic Medicine. 6: 350-356. PMID 29932521 DOI: 10.1002/Mgg3.377 |
0.386 |
|
2018 |
LaHue SC, Kim H, Pawlikowska L, Nelson J, Cooke DL, Hetts SW, Singh V. Frequency and characteristics associated with inherited thrombophilia in patients with intracranial dural arteriovenous fistula. Journal of Neurosurgery. 1-5. PMID 29624150 DOI: 10.3171/2017.10.Jns171987 |
0.357 |
|
2018 |
Nelson J, Bendjilali N, Weinsheimer SM, McCulloch CE, Ko NU, Zaroff JG, Lawton MT, Pawlikowska L, Kim H. Abstract WP426: Does Intracerebral Hemorrhage in Brain Arteriovenous Malformation Share Genetic Risk Factors With Primary Intracerebral Hemorrhage? Stroke. 49. DOI: 10.1161/Str.49.Suppl_1.Wp426 |
0.322 |
|
2016 |
Weinsheimer S, Bendjilali N, Nelson J, Guo DE, Zaroff JG, Sidney S, McCulloch CE, Al-Shahi Salman R, Berg JN, Koeleman BP, Simon M, Bostroem A, Fontanella M, Sturiale CL, Pola R, ... ... Pawlikowska L, et al. Genome-wide association study of sporadic brain arteriovenous malformations. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 26818729 DOI: 10.1136/Jnnp-2015-312272 |
0.401 |
|
2016 |
Choquet H, Trapani E, Goitre L, Trabalzini L, Akers A, Fontanella M, Hart BL, Morrison LA, Pawlikowska L, Kim H, Retta SF. Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1. Free Radical Biology & Medicine. 92: 100-109. PMID 26795600 DOI: 10.1016/J.Freeradbiomed.2016.01.008 |
0.315 |
|
2015 |
Tranah GJ, Yaffe K, Katzman SM, Lam ET, Pawlikowska L, Kwok PY, Schork NJ, Manini TM, Kritchevsky S, Thomas F, Newman AB, Harris TB, Coleman AL, Gorin MB, Helzner EP, et al. Mitochondrial DNA Heteroplasmy Associations With Neurosensory and Mobility Function in Elderly Adults. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 26328603 DOI: 10.1093/Gerona/Glv097 |
0.626 |
|
2015 |
Pawlikowska L, Nelson J, Guo DE, McCulloch CE, Lawton MT, Young WL, Kim H, Faughnan ME. 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. PMID 25847705 DOI: 10.1002/Ajmg.A.36936 |
0.366 |
|
2015 |
Kremer PH, Koeleman BP, Pawlikowska L, Weinsheimer S, Bendjilali N, Sidney S, Zaroff JG, Rinkel GJ, van den Berg LH, Ruigrok YM, de Kort GA, Veldink JH, Kim H, Klijn CJ. Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 524-9. PMID 25053769 DOI: 10.1136/Jnnp-2013-307276 |
0.358 |
|
2014 |
Choquet H, Pawlikowska L, Nelson J, McCulloch CE, Akers A, Baca B, Khan Y, Hart B, Morrison L, Kim H. Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity. Cerebrovascular Diseases (Basel, Switzerland). 38: 433-40. PMID 25472749 DOI: 10.1159/000369200 |
0.324 |
|
2014 |
Hackett CS, Quigley DA, Wong RA, Chen J, Cheng C, Song YK, Wei JS, Pawlikowska L, Bao Y, Goldenberg DD, Nguyen K, Gustafson WC, Rallapalli SK, Cho YJ, Cook JM, et al. Expression quantitative trait loci and receptor pharmacology implicate Arg1 and the GABA-A receptor as therapeutic targets in neuroblastoma. Cell Reports. 9: 1034-46. PMID 25437558 DOI: 10.1016/J.Celrep.2014.09.046 |
0.47 |
|
2014 |
Bendjilali N, Nelson J, Weinsheimer S, Sidney S, Zaroff JG, Hetts SW, Segal M, Pawlikowska L, McCulloch CE, Young WL, Kim H. Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms. Journal of Neurology, Neurosurgery, and Psychiatry. 85: 1280-3. PMID 24777168 DOI: 10.1136/Jnnp-2013-306461 |
0.413 |
|
2014 |
Choquet H, Nelson J, Pawlikowska L, McCulloch CE, Akers A, Baca B, Khan Y, Hart B, Morrison L, Kim H. Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation. Cerebrovascular Diseases (Basel, Switzerland). 37: 57-63. PMID 24401931 DOI: 10.1159/000356839 |
0.319 |
|
2013 |
Boshuisen K, Brundel M, de Kovel CG, Letteboer TG, Rinkel GJ, Westermann CJ, Kim H, Pawlikowska L, Koeleman BP, Klijn CJ. Polymorphisms in ACVRL1 and endoglin genes are not associated with sporadic and HHT-related brain AVMs in Dutch patients. Translational Stroke Research. 4: 375-8. PMID 24323303 DOI: 10.1007/S12975-012-0231-4 |
0.397 |
|
2013 |
Bendjilali N, Kim H, Weinsheimer S, Guo DE, Kwok PY, Zaroff JG, Sidney S, Lawton MT, McCulloch CE, Koeleman BP, Klijn CJ, Young WL, Pawlikowska L. A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation. Plos One. 8: e71434. PMID 24098321 DOI: 10.1371/Journal.Pone.0071434 |
0.547 |
|
2012 |
Weinsheimer S, Brettman AD, Pawlikowska L, Wu DC, Mancuso MR, Kuhnert F, Lawton MT, Sidney S, Zaroff JG, McCulloch CE, Young WL, Kuo C, Kim H. G Protein-Coupled Receptor 124 (GPR124) Gene Polymorphisms and Risk of Brain Arteriovenous Malformation. Translational Stroke Research. 3: 418-27. PMID 23329986 DOI: 10.1007/S12975-012-0202-9 |
0.411 |
|
2012 |
Khush KK, Pawlikowska L, Menza RL, Goldstein BA, Hayden V, Nguyen J, Kim H, Poon A, Sapru A, Matthay MA, Kwok PY, Young WL, Baxter-Lowe LA, Zaroff JG. Beta-adrenergic receptor polymorphisms and cardiac graft function in potential organ donors. American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons. 12: 3377-86. PMID 22994654 DOI: 10.1111/J.1600-6143.2012.04266.X |
0.563 |
|
2012 |
Westbroek EM, Pawlikowska L, Lawton MT, McCulloch CE, Young WL, Kim H. Brain-derived neurotrophic factor Val66Met polymorphism predicts worse functional outcome after surgery in patients with unruptured brain arteriovenous malformation. Stroke; a Journal of Cerebral Circulation. 43: 2255-7. PMID 22773554 DOI: 10.1161/Strokeaha.112.663096 |
0.316 |
|
2012 |
Tranah GJ, Lam ET, Katzman SM, Nalls MA, Zhao Y, Evans DS, Yokoyama JS, Pawlikowska L, Kwok PY, Mooney S, Kritchevsky S, Goodpaster BH, Newman AB, Harris TB, Manini TM, et al. Mitochondrial DNA sequence variation is associated with free-living activity energy expenditure in the elderly. Biochimica Et Biophysica Acta. 1817: 1691-700. PMID 22659402 DOI: 10.1016/J.Bbabio.2012.05.012 |
0.655 |
|
2012 |
Kangelaris KN, Sapru A, Calfee CS, Liu KD, Pawlikowska L, Witte JS, Vittinghoff E, Zhuo H, Auerbach AD, Ziv E, Matthay MA. The association between a Darc gene polymorphism and clinical outcomes in African American patients with acute lung injury. Chest. 141: 1160-9. PMID 22207676 DOI: 10.1378/Chest.11-1766 |
0.339 |
|
2012 |
Lam ET, Bracci PM, Holly EA, Chu C, Poon A, Wan E, White K, Kwok PY, Pawlikowska L, Tranah GJ. Mitochondrial DNA sequence variation and risk of pancreatic cancer. Cancer Research. 72: 686-95. PMID 22174369 DOI: 10.1158/0008-5472.Can-11-1682 |
0.652 |
|
2011 |
Weinsheimer SM, Xu H, Achrol AS, Stamova B, McCulloch CE, Pawlikowska L, Tian Y, Ko NU, Lawton MT, Steinberg GK, Chang SD, Jickling G, Ander BP, Kim H, Sharp FR, et al. Gene expression profiling of blood in brain arteriovenous malformation patients. Translational Stroke Research. 2: 575-87. PMID 22184505 DOI: 10.1007/S12975-011-0103-3 |
0.306 |
|
2011 |
Aouizerat BE, Vittinghoff E, Musone SL, Pawlikowska L, Kwok PY, Olgin JE, Tseng ZH. GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. Bmc Cardiovascular Disorders. 11: 29. PMID 21658281 DOI: 10.1186/1471-2261-11-29 |
0.755 |
|
2011 |
Mikhak B, Weinsheimer S, Pawlikowska L, Poon A, Kwok PY, Lawton MT, Chen Y, Zaroff JG, Sidney S, McCulloch CE, Young WL, Kim H. Angiopoietin-like 4 (ANGPTL4) gene polymorphisms and risk of brain arteriovenous malformations. Cerebrovascular Diseases (Basel, Switzerland). 31: 338-45. PMID 21212665 DOI: 10.1159/000322601 |
0.57 |
|
2011 |
Sapru A, Pawlikowska L, Liu KD, Khush KK, Ann-Baxter-Lowe L, Hayden V, Menza RL, Convery M, Poon A, Landeck M, Zaroff JG, Matthay MA. Single-nucleotide polymorphisms in the β-adrenergic receptor genes are associated with lung allograft utilization. The Journal of Heart and Lung Transplantation : the Official Publication of the International Society For Heart Transplantation. 30: 211-7. PMID 20869266 DOI: 10.1016/J.Healun.2010.08.011 |
0.349 |
|
2010 |
Njajou OT, Blackburn EH, Pawlikowska L, Mangino M, Damcott CM, Kwok PY, Spector TD, Newman AB, Harris TB, Cummings SR, Cawthon RM, Shuldiner AR, Valdes AM, Hsueh WC. A common variant in the telomerase RNA component is associated with short telomere length. Plos One. 5: e13048. PMID 20885959 DOI: 10.1371/Journal.Pone.0013048 |
0.486 |
|
2010 |
Otte C, Wüst S, Zhao S, Pawlikowska L, Kwok PY, Whooley MA. Glucocorticoid receptor gene, low-grade inflammation, and heart failure: the Heart and Soul study. The Journal of Clinical Endocrinology and Metabolism. 95: 2885-91. PMID 20371666 DOI: 10.1210/Jc.2009-2251 |
0.549 |
|
2010 |
Su H, Kim H, Pawlikowska L, Kitamura H, Shen F, Cambier S, Markovics J, Lawton MT, Sidney S, Bollen AW, Kwok PY, Reichardt L, Young WL, Yang GY, Nishimura SL. Reduced expression of integrin alphavbeta8 is associated with brain arteriovenous malformation pathogenesis. The American Journal of Pathology. 176: 1018-27. PMID 20019187 DOI: 10.2353/Ajpath.2010.090453 |
0.521 |
|
2010 |
Scherer ML, Nalls MA, Pawlikowska L, Ziv E, Mitchell G, Huntsman S, Hu D, Sutton-Tyrrell K, Lakatta EG, Hsueh WC, Newman AB, Tandon A, Kim L, Kwok PY, Sung A, et al. Admixture mapping of ankle-arm index: identification of a candidate locus associated with peripheral arterial disease. Journal of Medical Genetics. 47: 1-7. PMID 19586928 DOI: 10.1136/Jmg.2008.064808 |
0.52 |
|
2009 |
Weinsheimer S, Kim H, Pawlikowska L, Chen Y, Lawton MT, Sidney S, Kwok PY, McCulloch CE, Young WL. EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations. Circulation. Cardiovascular Genetics. 2: 476-82. PMID 20031623 DOI: 10.1161/Circgenetics.109.883595 |
0.59 |
|
2009 |
Tseng ZH, Vittinghoff E, Musone SL, Lin F, Whiteman D, Pawlikowska L, Kwok PY, Olgin JE, Aouizerat BE. Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 6: 1745-50. PMID 19959123 DOI: 10.1016/J.Hrthm.2009.08.031 |
0.757 |
|
2009 |
Otte C, Wüst S, Zhao S, Pawlikowska L, Kwok PY, Whooley MA. Glucocorticoid receptor gene and depression in patients with coronary heart disease: the Heart and Soul Study-2009 Curt Richter Award Winner. Psychoneuroendocrinology. 34: 1574-81. PMID 19783104 DOI: 10.1016/J.Psyneuen.2009.08.016 |
0.548 |
|
2009 |
Panici JA, Wang F, Bonkowski MS, Spong A, Bartke A, Pawlikowska L, Kwok PY, Masternak MM. Is altered expression of hepatic insulin-related genes in growth hormone receptor knockout mice due to GH resistance or a difference in biological life spans? The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 64: 1126-33. PMID 19706698 DOI: 10.1093/Gerona/Glp111 |
0.481 |
|
2009 |
Pawlikowska L, Hu D, Huntsman S, Sung A, Chu C, Chen J, Joyner AH, Schork NJ, Hsueh WC, Reiner AP, Psaty BM, Atzmon G, Barzilai N, Cummings SR, Browner WS, et al. Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity. Aging Cell. 8: 460-72. PMID 19489743 DOI: 10.1111/J.1474-9726.2009.00493.X |
0.556 |
|
2009 |
Cheng CY, Kao WH, Patterson N, Tandon A, Haiman CA, Harris TB, Xing C, John EM, Ambrosone CB, Brancati FL, Coresh J, Press MF, Parekh RS, Klag MJ, Meoni LA, ... ... Pawlikowska L, et al. Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X. Plos Genetics. 5: e1000490. PMID 19461885 DOI: 10.1371/Journal.Pgen.1000490 |
0.303 |
|
2009 |
Walston JD, Matteini AM, Nievergelt C, Lange LA, Fallin DM, Barzilai N, Ziv E, Pawlikowska L, Kwok P, Cummings SR, Kooperberg C, LaCroix A, Tracy RP, Atzmon G, Lange EM, et al. Inflammation and stress-related candidate genes, plasma interleukin-6 levels, and longevity in older adults. Experimental Gerontology. 44: 350-5. PMID 19249341 DOI: 10.1016/J.Exger.2009.02.004 |
0.57 |
|
2009 |
Kim H, Hysi PG, Pawlikowska L, Poon A, Burchard EG, Zaroff JG, Sidney S, Ko NU, Achrol AS, Lawton MT, McCulloch CE, Kwok PY, Young WL. Common variants in interleukin-1-Beta gene are associated with intracranial hemorrhage and susceptibility to brain arteriovenous malformation. Cerebrovascular Diseases (Basel, Switzerland). 27: 176-82. PMID 19092239 DOI: 10.1159/000185609 |
0.568 |
|
2009 |
Kim H, Pawlikowska L, Chen Y, Su H, Yang GY, Young WL. Brain arteriovenous malformation biology relevant to hemorrhage and implication for therapeutic development. Stroke; a Journal of Cerebral Circulation. 40: S95-7. PMID 19064791 DOI: 10.1161/Strokeaha.108.533216 |
0.343 |
|
2009 |
Khush KK, Pawlikowska L, Menza R, Hayden V, Babcock W, Sapru A, Matthay MA, Landeck M, Young W, Hoopes C, Baxter-Lowe LA, Zaroff JG. 348: Beta-Adrenergic Receptor Polymorphisms Are Associated with Cardiac Graft Function in Potential Organ Donors Journal of Heart and Lung Transplantation. 28. DOI: 10.1016/J.Healun.2008.11.355 |
0.327 |
|
2008 |
Kim H, Marchuk DA, Pawlikowska L, Chen Y, Su H, Yang GY, Young WL. Genetic considerations relevant to intracranial hemorrhage and brain arteriovenous malformations Acta Neurochirurgica, Supplementum. 199-206. PMID 19066109 DOI: 10.1007/978-3-211-09469-3_38 |
0.396 |
|
2008 |
Kim H, Hysi PG, Pawlikowska L, Choudhry S, González Burchard E, Kwok PY, Sidney S, McCulloch CE, Young WL. Population stratification in a case-control study of brain arteriovenous malformation in Latinos. Neuroepidemiology. 31: 224-8. PMID 18841030 DOI: 10.1159/000160215 |
0.501 |
|
2008 |
Tseng ZH, Aouizerat BE, Pawlikowska L, Vittinghoff E, Lin F, Whiteman D, Poon A, Herrington D, Howard TD, Varosy PD, Hulley SB, Malloy M, Kane J, Kwok PY, Olgin JE. Common beta-adrenergic receptor polymorphisms are not associated with risk of sudden cardiac death in patients with coronary artery disease. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 5: 814-21. PMID 18534365 DOI: 10.1016/J.Hrthm.2008.03.016 |
0.585 |
|
2008 |
Strautnieks SS, Byrne JA, Pawlikowska L, Cebecauerová D, Rayner A, Dutton L, Meier Y, Antoniou A, Stieger B, Arnell H, Ozçay F, Al-Hussaini HF, Bassas AF, Verkade HJ, Fischler B, et al. Severe bile salt export pump deficiency: 82 different ABCB11 mutations in 109 families. Gastroenterology. 134: 1203-14. PMID 18395098 DOI: 10.1053/J.Gastro.2008.01.038 |
0.318 |
|
2008 |
Ko NU, Rajendran P, Kim H, Rutkowski M, Pawlikowska L, Kwok PY, Higashida RT, Lawton MT, Smith WS, Zaroff JG, Young WL. Endothelial nitric oxide synthase polymorphism (-786T->C) and increased risk of angiographic vasospasm after aneurysmal subarachnoid hemorrhage. Stroke; a Journal of Cerebral Circulation. 39: 1103-8. PMID 18309169 DOI: 10.1161/Strokeaha.107.496596 |
0.518 |
|
2008 |
Marcus GM, Whooley MA, Glidden DV, Pawlikowska L, Zaroff JG, Olgin JE. Interleukin-6 and atrial fibrillation in patients with coronary artery disease: data from the Heart and Soul Study. American Heart Journal. 155: 303-9. PMID 18215601 DOI: 10.1016/J.Ahj.2007.09.006 |
0.348 |
|
2007 |
Achrol AS, Kim H, Pawlikowska L, Trudy Poon KY, McCulloch CE, Ko NU, Johnston SC, McDermott MW, Zaroff JG, Lawton MT, Kwok PY, Young WL. Association of tumor necrosis factor-alpha-238G>A and apolipoprotein E2 polymorphisms with intracranial hemorrhage after brain arteriovenous malformation treatment. Neurosurgery. 61: 731-9; discussion 74. PMID 17986934 DOI: 10.1227/01.Neu.0000298901.61849.A4 |
0.36 |
|
2007 |
Sabeti PC, Varilly P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, Byrne EH, McCarroll SA, Gaudet R, Schaffner SF, Lander ES, Frazer KA, Ballinger DG, ... ... Pawlikowska L, et al. Genome-wide detection and characterization of positive selection in human populations. Nature. 449: 913-8. PMID 17943131 DOI: 10.1038/Nature06250 |
0.31 |
|
2007 |
Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, ... ... Pawlikowska L, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature. 449: 851-61. PMID 17943122 DOI: 10.1038/Nature06258 |
0.541 |
|
2007 |
Tingley WG, Pawlikowska L, Zaroff JG, Kim T, Nguyen T, Young SG, Vranizan K, Kwok PY, Whooley MA, Conklin BR. Gene-trapped mouse embryonic stem cell-derived cardiac myocytes and human genetics implicate AKAP10 in heart rhythm regulation. Proceedings of the National Academy of Sciences of the United States of America. 104: 8461-6. PMID 17485678 DOI: 10.1073/Pnas.0610393104 |
0.545 |
|
2007 |
Reich D, Patterson N, Ramesh V, De Jager PL, McDonald GJ, Tandon A, Choy E, Hu D, Tamraz B, Pawlikowska L, Wassel-Fyr C, Huntsman S, Waliszewska A, Rossin E, Li R, et al. Admixture mapping of an allele affecting interleukin 6 soluble receptor and interleukin 6 levels. American Journal of Human Genetics. 80: 716-26. PMID 17357077 DOI: 10.1086/513206 |
0.737 |
|
2007 |
Shah SJ, Tingley WG, Zaroff JG, Pawlikowska L, Kwok P, Whooley MA. Genetic Determinants of Cardiac Contractile Function in Caucasians Journal of Cardiac Failure. 13: S73-S74. DOI: 10.1016/J.Cardfail.2007.06.305 |
0.511 |
|
2006 |
Zaroff JG, Pawlikowska L, Miss JC, Yarlagadda S, Ha C, Achrol A, Kwok PY, McCulloch CE, Lawton MT, Ko N, Smith W, Young WL. Adrenoceptor polymorphisms and the risk of cardiac injury and dysfunction after subarachnoid hemorrhage. Stroke; a Journal of Cerebral Circulation. 37: 1680-5. PMID 16728691 DOI: 10.1161/01.Str.0000226461.52423.Dd |
0.548 |
|
2006 |
Pawlikowska L, Poon KY, Achrol AS, McCulloch CE, Ha C, Lum K, Zaroff JG, Ko NU, Johnston SC, Sidney S, Marchuk DA, Lawton MT, Kwok PY, Young WL. Apolipoprotein E epsilon 2 is associated with new hemorrhage risk in brain arteriovenous malformations. Neurosurgery. 58: 838-43; discussion 8. PMID 16639317 DOI: 10.1227/01.Neu.0000209605.18358.E5 |
0.539 |
|
2006 |
Achrol AS, Pawlikowska L, McCulloch CE, Poon KY, Ha C, Zaroff JG, Johnston SC, Lee C, Lawton MT, Sidney S, Marchuk DA, Kwok PY, Young WL. Tumor necrosis factor-alpha-238G>A promoter polymorphism is associated with increased risk of new hemorrhage in the natural course of patients with brain arteriovenous malformations. Stroke; a Journal of Cerebral Circulation. 37: 231-4. PMID 16322490 DOI: 10.1161/01.Str.0000195133.98378.4B |
0.388 |
|
2006 |
Chen Y, Pawlikowska L, Yao JS, Shen F, Zhai W, Achrol AS, Lawton MT, Kwok PY, Yang GY, Young WL. Interleukin-6 involvement in brain arteriovenous malformations. Annals of Neurology. 59: 72-80. PMID 16278864 DOI: 10.1002/Ana.20697 |
0.51 |
|
2006 |
Zaroff JG, Pawlikowska L, Miss JC, Yarlagadda S, Ha C, Achrol A, Kwok PY, McCulloch CE, Lawton MT, Ko N, Smith W, Young WL. Response to letter by Atanassova [7] Stroke. 37: 2873. DOI: 10.1161/01.Str.0000248200.15086.97 |
0.498 |
|
2005 |
Pawlikowska L, Tran MN, Achrol AS, Ha C, Burchard E, Choudhry S, Zaroff J, Lawton MT, Castro R, McCulloch CE, Marchuk D, Kwok PY, Young WL. Polymorphisms in transforming growth factor-beta-related genes ALK1 and ENG are associated with sporadic brain arteriovenous malformations. Stroke; a Journal of Cerebral Circulation. 36: 2278-80. PMID 16179574 DOI: 10.1161/01.Str.0000182253.91167.Fa |
0.569 |
|
2005 |
Belmont JW, Boudreau A, Leal SM, Hardenbol P, Pasternak S, Wheeler DA, Willis TD, Yu F, Yang H, Gao Y, Hu H, Hu W, Li C, Lin W, Liu S, ... ... Pawlikowska L, et al. A haplotype map of the human genome Nature. 437: 1299-1320. DOI: 10.1038/Nature04226 |
0.349 |
|
2004 |
Carlton VE, Pawlikowska L, Bull LN. Molecular basis of intrahepatic cholestasis. Annals of Medicine. 36: 606-17. PMID 15768832 DOI: 10.1080/07853890410018916 |
0.303 |
|
2004 |
Pawlikowska L, Tran MN, Achrol AS, McCulloch CE, Ha C, Lind DL, Hashimoto T, Zaroff J, Lawton MT, Marchuk DA, Kwok PY, Young WL. Polymorphisms in genes involved in inflammatory and angiogenic pathways and the risk of hemorrhagic presentation of brain arteriovenous malformations. Stroke; a Journal of Cerebral Circulation. 35: 2294-300. PMID 15331795 DOI: 10.1161/01.Str.0000141932.44613.B1 |
0.566 |
|
2004 |
Pawlikowska L, Groen A, Eppens EF, Kunne C, Ottenhoff R, Looije N, Knisely AS, Killeen NP, Bull LN, Elferink RP, Freimer NB. A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion. Human Molecular Genetics. 13: 881-92. PMID 14976163 DOI: 10.1093/Hmg/Ddh100 |
0.568 |
|
1998 |
Bull LN, Van Eijk MJT, Pawlikowska L, DeYoung JA, Juijn JA, Liao M, Klomp LWJ, Lomri N, Berger R, Scharschmidt BF, Knisely AS, Houwen RHJ, Freimer NB. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis Nature Genetics. 18: 219-224. PMID 9500542 DOI: 10.1038/Ng0398-219 |
0.307 |
|
Show low-probability matches. |