| Year |
Citation |
Score |
| 2021 |
Yoon S, Wang X, Vongpunsawad S, Tromp G, Kuivaniemi H. Editorial: FDA-Approved Drug Repositioning for P-Glycoprotein Overexpressing Resistant Cancer. Frontiers in Oncology. 11: 632657. PMID 33816271 DOI: 10.3389/fonc.2021.632657 |
0.5 |
|
| 2020 |
Miszczuk M, Müller V, Althoff CE, Stroux A, Widhalm D, Dobberstein A, Greiner A, Kuivaniemi H, Hinterseher I. Association of simple renal cysts and chronic kidney disease with large abdominal aortic aneurysm. Bmc Nephrology. 21: 201. PMID 32471416 DOI: 10.1186/S12882-020-01841-6 |
0.321 |
|
| 2019 |
Faggion Vinholo T, Brownstein AJ, Ziganshin BA, Zafar MA, Kuivaniemi H, Body SC, Bale AE, Elefteriades JA. Genes Associated with Thoracic Aortic Aneurysm and Dissection: 2019 Update and Clinical Implications. Aorta (Stamford, Conn.). 7: 99-107. PMID 31842235 DOI: 10.1055/s-0039-3400233 |
0.31 |
|
| 2019 |
Sharma N, Dev R, Ruiz-Rosado JD, Partida-Sanchez S, Guerau-de-Arellano M, Dhakal P, Kuivaniemi H, Hans CP. Pharmacological inhibition of Notch signaling regresses pre-established abdominal aortic aneurysm. Scientific Reports. 9: 13458. PMID 31530833 DOI: 10.1038/S41598-019-49682-0 |
0.355 |
|
| 2019 |
Simba H, Kuivaniemi H, Lutje V, Tromp G, Sewram V. Systematic Review of Genetic Factors in the Etiology of Esophageal Squamous Cell Carcinoma in African Populations. Frontiers in Genetics. 10: 642. PMID 31428123 DOI: 10.3389/Fgene.2019.00642 |
0.335 |
|
| 2019 |
Edwards TL, Giri A, Hellwege JN, Hartmann KE, Stewart EA, Jeff JM, Bray MJ, Pendergrass SA, Torstenson ES, Keaton JM, Jones SH, Gogoi RP, Kuivaniemi H, Jackson KL, Kho AN, et al. A -Ethnic Genome-Wide Association Study of Uterine Fibroids. Frontiers in Genetics. 10: 511. PMID 31249589 DOI: 10.3389/Fgene.2019.00511 |
0.342 |
|
| 2019 |
Kuivaniemi H, Tromp G. Type III collagen (COL3A1): Gene and protein structure, tissue distribution, and associated diseases. Gene. PMID 31075413 DOI: 10.1016/J.Gene.2019.05.003 |
0.313 |
|
| 2018 |
Brownstein AJ, Kostiuk V, Ziganshin BA, Zafar MA, Kuivaniemi H, Body SC, Bale AE, Elefteriades JA. Genes Associated with Thoracic Aortic Aneurysm and Dissection: 2018 Update and Clinical Implications. Aorta (Stamford, Conn.). 6: 13-20. PMID 30079932 DOI: 10.1055/s-0038-1639612 |
0.32 |
|
| 2018 |
Makrygiannis G, Mourmoura E, Spanos K, Roussas N, Kuivaniemi H, Sakalihasan N, Tsezou A, Giannoukas A. Risk Factor Assessment in a Greek Cohort of Patients With Large Abdominal Aortic Aneurysms. Angiology. 3319718774474. PMID 29739236 DOI: 10.1177/0003319718774474 |
0.412 |
|
| 2018 |
Turcot V, Lu Y, Highland HM, Schurmann C, Justice AE, Fine RS, Bradfield JP, Esko T, Giri A, Graff M, Guo X, Hendricks AE, Karaderi T, Lempradl A, Locke AE, ... ... Kuivaniemi H, et al. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics. 50: 26-41. PMID 29273807 DOI: 10.1038/S41588-017-0011-X |
0.325 |
|
| 2017 |
Harrison SC, Holmes MV, Burgess S, Asselbergs FW, Jones GT, Baas AF, van 't Hof FN, de Bakker PIW, Blankensteijn JD, Powell JT, Saratzis A, de Borst GJ, Swerdlow DI, van der Graaf Y, van Rij AM, ... ... Kuivaniemi H, et al. Genetic Association of Lipids and Lipid Drug Targets With Abdominal Aortic Aneurysm: A Meta-analysis. Jama Cardiology. PMID 29188294 DOI: 10.1001/Jamacardio.2017.4293 |
0.39 |
|
| 2017 |
Brownstein AJ, Ziganshin BA, Kuivaniemi H, Body SC, Bale AE, Elefteriades JA. Genes Associated with Thoracic Aortic Aneurysm and Dissection: An Update and Clinical Implications. Aorta (Stamford, Conn.). 5: 11-20. PMID 28868310 DOI: 10.12945/j.aorta.2017.17.003 |
0.325 |
|
| 2017 |
Sachdeva J, Mahajan A, Cheng J, Baeten JT, Lilly B, Kuivaniemi H, Hans CP. Smooth muscle cell-specific Notch1 haploinsufficiency restricts the progression of abdominal aortic aneurysm by modulating CTGF expression. Plos One. 12: e0178538. PMID 28562688 DOI: 10.1371/Journal.Pone.0178538 |
0.347 |
|
| 2017 |
Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM, Rüeger S, Thorleifsson G, Justice AE, Lamparter D, Stirrups KE, ... ... Kuivaniemi H, et al. Rare and low-frequency coding variants alter human adult height. Nature. PMID 28146470 DOI: 10.1038/Nature21039 |
0.343 |
|
| 2016 |
Li M, Li Y, Weeks O, Mijatovic V, Teumer A, Huffman JE, Tromp G, Fuchsberger C, Gorski M, Lyytikäinen LP, Nutile T, Sedaghat S, Sorice R, Tin A, Yang Q, ... ... Kuivaniemi H, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology : Jasn. PMID 27920155 DOI: 10.1681/Asn.2016020131 |
0.346 |
|
| 2016 |
Jones GT, Tromp G, Kuivaniemi H, Gretarsdottir S, Baas AF, Giusti B, Strauss E, van 't Hof FN, Webb T, Erdman R, Ritchie MD, Elmore JR, Verma A, Pendergrass S, Kullo IJ, et al. Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci. Circulation Research. PMID 27899403 DOI: 10.1161/Circresaha.116.308765 |
0.404 |
|
| 2016 |
De R, Verma SS, Holzinger E, Hall M, Burt A, Carrell DS, Crosslin DR, Jarvik GP, Kuivaniemi H, Kullo IJ, Lange LA, Lanktree MB, Larson EB, North KE, Reiner AP, et al. Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts. Human Genetics. PMID 27848076 DOI: 10.1007/S00439-016-1738-7 |
0.302 |
|
| 2016 |
Verma A, Verma SS, Pendergrass SA, Crawford DC, Crosslin DR, Kuivaniemi H, Bush WS, Bradford Y, Kullo I, Bielinski SJ, Li R, Denny JC, Peissig P, Hebbring S, De Andrade M, et al. eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants. Bmc Medical Genomics. 9: 32. PMID 27535653 DOI: 10.1186/S12920-016-0191-8 |
0.31 |
|
| 2016 |
Verma A, Basile AO, Bradford Y, Kuivaniemi H, Tromp G, Carey D, Gerhard GS, Crowe JE, Ritchie MD, Pendergrass SA. Phenome-Wide Association Study to Explore Relationships between Immune System Related Genetic Loci and Complex Traits and Diseases. Plos One. 11: e0160573. PMID 27508393 DOI: 10.1371/Journal.Pone.0160573 |
0.338 |
|
| 2016 |
van 't Hof FN, Ruigrok YM, Lee CH, Ripke S, Anderson G, de Andrade M, Baas AF, Blankensteijn JD, Böttinger EP, Bown MJ, Broderick J, Bijlenga P, Carrell DS, Crawford DC, Crosslin DR, ... ... Kuivaniemi H, et al. Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms. Journal of the American Heart Association. 5. PMID 27418160 DOI: 10.1161/Jaha.115.002603 |
0.395 |
|
| 2016 |
Zhang C, van der Voort D, Shi H, Zhang R, Qing Y, Hiraoka S, Takemoto M, Yokote K, Moxon JV, Norman P, Rittié L, Kuivaniemi H, Atkins GB, Gerson SL, Shi GP, et al. Matricellular protein CCN3 mitigates abdominal aortic aneurysm. The Journal of Clinical Investigation. PMID 26974158 DOI: 10.1172/Jci82337 |
0.368 |
|
| 2015 |
Kuivaniemi H, Ryer EJ, Elmore JR, Tromp G. In response: abdominal aortic aneurysms: do not underestimate the role of diabetes. Expert Review of Cardiovascular Therapy. 13: 1291-2. PMID 26469388 DOI: 10.1586/14779072.2015.1100538 |
0.327 |
|
| 2015 |
Kuivaniemi H, Ryer EJ, Elmore JR, Tromp G. Understanding the pathogenesis of abdominal aortic aneurysms. Expert Review of Cardiovascular Therapy. 13: 975-87. PMID 26308600 DOI: 10.1586/14779072.2015.1074861 |
0.406 |
|
| 2015 |
Ryer EJ, Garvin RP, Thomas B, Kuivaniemi H, Franklin DP, Elmore JR. Patients with familial abdominal aortic aneurysms are at increased risk for endoleak and secondary intervention following elective endovascular aneurysm repair. Journal of Vascular Surgery. 62: 1119-1124.e9. PMID 26254452 DOI: 10.1016/J.Jvs.2015.06.205 |
0.356 |
|
| 2015 |
Mosley JD, Shaffer CM, Van Driest SL, Weeke PE, Wells QS, Karnes JH, Velez Edwards DR, Wei WQ, Teixeira PL, Bastarache L, Crawford DC, Li R, Manolio TA, Bottinger EP, McCarty CA, ... ... Kuivaniemi H, et al. A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. The Pharmacogenomics Journal. PMID 26169577 DOI: 10.1038/Tpj.2015.51 |
0.322 |
|
| 2015 |
Ryer EJ, Ronning KE, Erdman R, Schworer CM, Elmore JR, Peeler TC, Nevius CD, Lillvis JH, Garvin RP, Franklin DP, Kuivaniemi H, Tromp G. The potential role of DNA methylation in abdominal aortic aneurysms. International Journal of Molecular Sciences. 16: 11259-75. PMID 25993294 DOI: 10.3390/Ijms160511259 |
0.361 |
|
| 2015 |
Pahl MC, Erdman R, Kuivaniemi H, Lillvis JH, Elmore JR, Tromp G. Transcriptional (ChIP-Chip) Analysis of ELF1, ETS2, RUNX1 and STAT5 in Human Abdominal Aortic Aneurysm. International Journal of Molecular Sciences. 16: 11229-58. PMID 25993293 DOI: 10.3390/Ijms160511229 |
0.361 |
|
| 2015 |
Hinterseher I, Schworer CM, Lillvis JH, Stahl E, Erdman R, Gatalica Z, Tromp G, Kuivaniemi H. Immunohistochemical analysis of the natural killer cell cytotoxicity pathway in human abdominal aortic aneurysms. International Journal of Molecular Sciences. 16: 11196-212. PMID 25993291 DOI: 10.3390/Ijms160511196 |
0.332 |
|
| 2015 |
Dai X, Shen J, Annam NP, Jiang H, Levi E, Schworer CM, Tromp G, Arora A, Higgins M, Wang XF, Yang M, Li HJ, Zhang K, Kuivaniemi H, Li L. SMAD3 deficiency promotes vessel wall remodeling, collagen fiber reorganization and leukocyte infiltration in an inflammatory abdominal aortic aneurysm mouse model. Scientific Reports. 5: 10180. PMID 25985281 DOI: 10.1038/Srep10180 |
0.325 |
|
| 2015 |
Hall MA, Verma SS, Wallace J, Lucas A, Berg RL, Connolly J, Crawford DC, Crosslin DR, de Andrade M, Doheny KF, Haines JL, Harley JB, Jarvik GP, Kitchner T, Kuivaniemi H, et al. Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network. Genetic Epidemiology. 39: 376-84. PMID 25982363 DOI: 10.1002/Gepi.21902 |
0.33 |
|
| 2015 |
Crosslin DR, Carrell DS, Burt A, Kim DS, Underwood JG, Hanna DS, Comstock BA, Baldwin E, de Andrade M, Kullo IJ, Tromp G, Kuivaniemi H, Borthwick KM, McCarty CA, Peissig PL, et al. Genetic variation in the HLA region is associated with susceptibility to herpes zoster. Genes and Immunity. 16: 1-7. PMID 25297839 DOI: 10.1038/Gene.2014.51 |
0.324 |
|
| 2015 |
Ryer EJ, Garvin RP, Schworer CM, Bernard-Eckroth KR, Tromp G, Franklin DP, Elmore JR, Kuivaniemi H. Proinflammatory role of stem cells in abdominal aortic aneurysms. Journal of Vascular Surgery. 62: 1303-1311.e4. PMID 24997808 DOI: 10.1016/J.Jvs.2014.04.067 |
0.328 |
|
| 2015 |
Thomas BK, Ryer EJ, Garvin RP, Kuivaniemi H, Franklin DP, Elmore JR. Patients With Familial Abdominal Aortic Aneurysms Are at Increased Risk for Type 1 Endoleak Following Elective Endovascular Aneurysm Repair Journal of Vascular Surgery. 61: 584-585. DOI: 10.1016/J.Jvs.2014.11.038 |
0.384 |
|
| 2014 |
Courtois A, Nusgens BV, Hustinx R, Namur G, Gomez P, Kuivaniemi H, Defraigne JO, Colige AC, Sakalihasan N. Gene expression study in positron emission tomography-positive abdominal aortic aneurysms identifies CCL18 as a potential biomarker for rupture risk. Molecular Medicine (Cambridge, Mass.). 20: 697-706. PMID 25517227 DOI: 10.2119/Molmed.2014.00065 |
0.386 |
|
| 2014 |
Smelser DT, Tromp G, Elmore JR, Kuivaniemi H, Franklin DP, Kirchner HL, Carey DJ. Population risk factor estimates for abdominal aortic aneurysm from electronic medical records: a case control study. Bmc Cardiovascular Disorders. 14: 174. PMID 25475588 DOI: 10.1186/1471-2261-14-174 |
0.343 |
|
| 2014 |
Tromp G, Weinsheimer S, Ronkainen A, Kuivaniemi H. Molecular basis and genetic predisposition to intracranial aneurysm. Annals of Medicine. 46: 597-606. PMID 25117779 DOI: 10.3109/07853890.2014.949299 |
0.404 |
|
| 2014 |
Makrygiannis G, Courtois A, Drion P, Defraigne JO, Kuivaniemi H, Sakalihasan N. Sex differences in abdominal aortic aneurysm: the role of sex hormones. Annals of Vascular Surgery. 28: 1946-58. PMID 25106102 DOI: 10.1016/J.Avsg.2014.07.008 |
0.341 |
|
| 2014 |
Sakalihasan N, Defraigne JO, Kerstenne MA, Cheramy-Bien JP, Smelser DT, Tromp G, Kuivaniemi H. Family members of patients with abdominal aortic aneurysms are at increased risk for aneurysms: analysis of 618 probands and their families from the Liège AAA Family Study. Annals of Vascular Surgery. 28: 787-97. PMID 24365082 DOI: 10.1016/J.Avsg.2013.11.005 |
0.359 |
|
| 2014 |
Morris DR, Biros E, Cronin O, Kuivaniemi H, Golledge J. The association of genetic variants of matrix metalloproteinases with abdominal aortic aneurysm: a systematic review and meta-analysis. Heart (British Cardiac Society). 100: 295-302. PMID 23813847 DOI: 10.1136/Heartjnl-2013-304129 |
0.356 |
|
| 2014 |
Estrelinha M, Hinterseher I, Kuivaniemi H. Gene expression studies in human abdominal aortic aneurysm Reviews in Vascular Medicine. 2: 77-82. DOI: 10.1016/J.Rvm.2014.02.001 |
0.411 |
|
| 2013 |
Mosley JD, Van Driest SL, Larkin EK, Weeke PE, Witte JS, Wells QS, Karnes JH, Guo Y, Bastarache L, Olson LM, McCarty CA, Pacheco JA, Jarvik GP, Carrell DS, Larson EB, ... ... Kuivaniemi H, et al. Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data. Plos One. 8: e81503. PMID 24349080 DOI: 10.1371/Journal.Pone.0081503 |
0.35 |
|
| 2013 |
Jones GT, Bown MJ, Gretarsdottir S, Romaine SP, Helgadottir A, Yu G, Tromp G, Norman PE, Jin C, Baas AF, Blankensteijn JD, Kullo IJ, Phillips LV, Williams MJ, Topless R, ... ... Kuivaniemi H, et al. A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm. Human Molecular Genetics. 22: 2941-7. PMID 23535823 DOI: 10.1093/Hmg/Ddt141 |
0.406 |
|
| 2013 |
Golledge J, Kuivaniemi H. Genetics of abdominal aortic aneurysm. Current Opinion in Cardiology. 28: 290-6. PMID 23478885 DOI: 10.1097/Hco.0B013E32835F0D55 |
0.388 |
|
| 2013 |
Hinterseher I, Erdman R, Elmore JR, Stahl E, Pahl MC, Derr K, Golden A, Lillvis JH, Cindric MC, Jackson K, Bowen WD, Schworer CM, Chernousov MA, Franklin DP, Gray JL, ... ... Kuivaniemi H, et al. Novel pathways in the pathobiology of human abdominal aortic aneurysms. Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology. 80: 1-10. PMID 22797469 DOI: 10.1159/000339303 |
0.381 |
|
| 2013 |
Smelser D, Tromp G, Elmore J, Kuivaniemi H, Ryer E, Bock J, Colonie R, Borthwick K, Franklin D, Carey D. PS2-8: ePhenotyping for Abdominal Aortic Aneurysm Clinical Medicine & Research. 11: 152-152. DOI: 10.3121/Cmr.2013.1176.Ps2-8 |
0.329 |
|
| 2012 |
Hans CP, Koenig SN, Huang N, Cheng J, Beceiro S, Guggilam A, Kuivaniemi H, Partida-Sánchez S, Garg V. Inhibition of Notch1 signaling reduces abdominal aortic aneurysm in mice by attenuating macrophage-mediated inflammation. Arteriosclerosis, Thrombosis, and Vascular Biology. 32: 3012-23. PMID 23087364 DOI: 10.1161/Atvbaha.112.254219 |
0.334 |
|
| 2012 |
Helgadottir A, Gretarsdottir S, Thorleifsson G, Holm H, Patel RS, Gudnason T, Jones GT, van Rij AM, Eapen DJ, Baas AF, Tregouet DA, Morange PE, Emmerich J, Lindblad B, Gottsäter A, ... ... Kuivaniemi H, et al. Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. Journal of the American College of Cardiology. 60: 722-9. PMID 22898070 DOI: 10.1016/J.Jacc.2012.01.078 |
0.325 |
|
| 2012 |
Kuivaniemi H, Elmore JR. Opportunities in abdominal aortic aneurysm research: epidemiology, genetics, and pathophysiology. Annals of Vascular Surgery. 26: 862-70. PMID 22794334 DOI: 10.1016/J.Avsg.2012.02.005 |
0.412 |
|
| 2012 |
Pahl MC, Derr K, Gäbel G, Hinterseher I, Elmore JR, Schworer CM, Peeler TC, Franklin DP, Gray JL, Carey DJ, Tromp G, Kuivaniemi H. MicroRNA expression signature in human abdominal aortic aneurysms. Bmc Medical Genomics. 5: 25. PMID 22704053 DOI: 10.1186/1755-8794-5-25 |
0.382 |
|
| 2012 |
Hinterseher I, Gäbel G, Corvinus F, Lück C, Saeger HD, Bergert H, Tromp G, Kuivaniemi H. Presence of Borrelia burgdorferi sensu lato antibodies in the serum of patients with abdominal aortic aneurysms European Journal of Clinical Microbiology and Infectious Diseases. 31: 781-789. PMID 21842293 DOI: 10.1007/S10096-011-1375-Y |
0.361 |
|
| 2011 |
Lillvis JH, Erdman R, Schworer CM, Golden A, Derr K, Gatalica Z, Cox LA, Shen J, Vander Heide RS, Lenk GM, Hlavaty L, Li L, Elmore JR, Franklin DP, Gray JL, ... ... Kuivaniemi H, et al. Regional expression of HOXA4 along the aorta and its potential role in human abdominal aortic aneurysms. Bmc Physiology. 11: 9. PMID 21627813 DOI: 10.1186/1472-6793-11-9 |
0.394 |
|
| 2011 |
Hinterseher I, Erdman R, Donoso LA, Vrabec TR, Schworer CM, Lillvis JH, Boddy AM, Derr K, Golden A, Bowen WD, Gatalica Z, Tapinos N, Elmore JR, Franklin DP, Gray JL, ... ... Kuivaniemi H, et al. Role of complement cascade in abdominal aortic aneurysms. Arteriosclerosis, Thrombosis, and Vascular Biology. 31: 1653-60. PMID 21493888 DOI: 10.1161/Atvbaha.111.227652 |
0.393 |
|
| 2011 |
Lillvis JH, Kyo Y, Tromp G, Lenk GM, Li M, Lu Q, Igo RP, Sakalihasan N, Ferrell RE, Schworer CM, Gatalica Z, Land S, Kuivaniemi H. Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19. Bmc Medical Genetics. 12: 14. PMID 21247474 DOI: 10.1186/1471-2350-12-14 |
0.424 |
|
| 2011 |
Hinterseher I, Tromp G, Kuivaniemi H. Genes and abdominal aortic aneurysm. Annals of Vascular Surgery. 25: 388-412. PMID 21146954 DOI: 10.1016/J.Avsg.2010.09.004 |
0.441 |
|
| 2010 |
Gretarsdottir S, Baas AF, Thorleifsson G, Holm H, den Heijer M, de Vries JP, Kranendonk SE, Zeebregts CJ, van Sterkenburg SM, Geelkerken RH, van Rij AM, Williams MJ, Boll AP, Kostic JP, Jonasdottir A, ... ... Kuivaniemi H, et al. Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. Nature Genetics. 42: 692-7. PMID 20622881 DOI: 10.1038/Ng.622 |
0.403 |
|
| 2010 |
Tromp G, Kuivaniemi H, Hinterseher I, Carey DJ. Novel genetic mechanisms for aortic aneurysms. Current Atherosclerosis Reports. 12: 259-66. PMID 20446064 DOI: 10.1007/S11883-010-0111-X |
0.416 |
|
| 2010 |
Haldar SM, Lu Y, Jeyaraj D, Kawanami D, Cui Y, Eapen SJ, Hao C, Li Y, Doughman YQ, Watanabe M, Shimizu K, Kuivaniemi H, Sadoshima J, Margulies KB, Cappola TP, et al. Klf15 deficiency is a molecular link between heart failure and aortic aneurysm formation. Science Translational Medicine. 2: 26ra26. PMID 20375365 DOI: 10.1126/Scitranslmed.3000502 |
0.326 |
|
| 2009 |
Nischan J, Gatalica Z, Curtis M, Lenk GM, Tromp G, Kuivaniemi H. Binding sites for ETS family of transcription factors dominate the promoter regions of differentially expressed genes in abdominal aortic aneurysms. Circulation. Cardiovascular Genetics. 2: 565-72. PMID 20031636 DOI: 10.1161/Circgenetics.108.843854 |
0.355 |
|
| 2009 |
Tromp G, Kuivaniemi H. Developments in Genomics to Improve Understanding, Diagnosis and Management of Aneurysms and Peripheral Artery Disease European Journal of Vascular and Endovascular Surgery. 38: 676-682. PMID 19783185 DOI: 10.1016/J.Ejvs.2009.08.010 |
0.337 |
|
| 2009 |
Elmore JR, Obmann MA, Kuivaniemi H, Tromp G, Gerhard GS, Franklin DP, Boddy AM, Carey DJ. Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association. Journal of Vascular Surgery. 49: 1525-31. PMID 19497516 DOI: 10.1016/J.Jvs.2009.07.098 |
0.412 |
|
| 2008 |
Boddy AM, Lenk GM, Lillvis JH, Nischan J, Kyo Y, Kuivaniemi H. Basic research studies to understand aneurysm disease. Drug News & Perspectives. 21: 142-8. PMID 18560612 DOI: 10.1358/Dnp.2008.21.3.1203410 |
0.405 |
|
| 2008 |
Kuivaniemi H, Platsoucas CD, Tilson MD. Aortic aneurysms: an immune disease with a strong genetic component. Circulation. 117: 242-52. PMID 18195185 DOI: 10.1161/Circulationaha.107.690982 |
0.392 |
|
| 2008 |
Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, Karkera J, Mahurkar S, Lisch W, Dupps WJ, White PS, Winters RS, Kim C, Rapuano CJ, Sutphin J, Reidy J, Hu FR, et al. Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function. American Journal of Medical Genetics. Part A. 146: 271-83. PMID 18176953 DOI: 10.1002/Ajmg.A.32201 |
0.31 |
|
| 2008 |
Helgadottir A, Thorleifsson G, Magnusson KP, Grétarsdottir S, Steinthorsdottir V, Manolescu A, Jones GT, Rinkel GJ, Blankensteijn JD, Ronkainen A, Jääskeläinen JE, Kyo Y, Lenk GM, Sakalihasan N, Kostulas K, ... ... Kuivaniemi H, et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nature Genetics. 40: 217-24. PMID 18176561 DOI: 10.1038/Ng.72 |
0.388 |
|
| 2007 |
Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, White PS, Winters RS, Lisch W, Henn W, Denninger E, Krause M, Wasson P, Ebenezer N, Mahurkar S, Nickerson ML. Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy. Investigative Ophthalmology & Visual Science. 48: 5007-12. PMID 17962451 DOI: 10.1167/Iovs.07-0845 |
0.327 |
|
| 2007 |
Weinsheimer S, Lenk GM, van der Voet M, Land S, Ronkainen A, Alafuzoff I, Kuivaniemi H, Tromp G. Integration of expression profiles and genetic mapping data to identify candidate genes in intracranial aneurysm. Physiological Genomics. 32: 45-57. PMID 17878320 DOI: 10.1152/Physiolgenomics.00015.2007 |
0.355 |
|
| 2007 |
Weinsheimer S, Goddard KA, Parrado AR, Lu Q, Sinha M, Lebedeva ER, Ronkainen A, Niemelä M, Khusnutdinova EK, Khusainova RI, Helin K, Jääskeläinen JE, Sakovich VP, Land S, Kuivaniemi H, et al. Association of kallikrein gene polymorphisms with intracranial aneurysms. Stroke; a Journal of Cerebral Circulation. 38: 2670-6. PMID 17761919 DOI: 10.1161/Strokeaha.107.486225 |
0.369 |
|
| 2007 |
Lenk GM, Tromp G, Weinsheimer S, Gatalica Z, Berguer R, Kuivaniemi H. Whole genome expression profiling reveals a significant role for immune function in human abdominal aortic aneurysms. Bmc Genomics. 8: 237. PMID 17634102 DOI: 10.1186/1471-2164-8-237 |
0.404 |
|
| 2007 |
Aziz F, Kuivaniemi H. Role of matrix metalloproteinase inhibitors in preventing abdominal aortic aneurysm. Annals of Vascular Surgery. 21: 392-401. PMID 17484978 DOI: 10.1016/J.Avsg.2006.11.001 |
0.366 |
|
| 2007 |
Wassef M, Upchurch GR, Kuivaniemi H, Thompson RW, Tilson MD. Challenges and opportunities in abdominal aortic aneurysm research. Journal of Vascular Surgery. 45: 192-8. PMID 17210410 DOI: 10.1016/J.Jvs.2006.09.004 |
0.369 |
|
| 2007 |
Goddard KA, Tromp G, Romero R, Olson JM, Lu Q, Xu Z, Parimi N, Nien JK, Gomez R, Behnke E, Solari M, Espinoza J, Santolaya J, Chaiworapongsa T, Lenk GM, ... ... Kuivaniemi H, et al. Candidate-gene association study of mothers with pre-eclampsia, and their infants, analyzing 775 SNPs in 190 genes. Human Heredity. 63: 1-16. PMID 17179726 DOI: 10.1159/000097926 |
0.354 |
|
| 2006 |
Tromp G, Ogata T, Gregoire L, Goddard KA, Skunca M, Lancaster WD, Parrado AR, Lu Q, Shibamura H, Sakalihasan N, Limet R, Mackean GL, Arthur C, Sueda T, Kuivaniemi H. HLA-DQA is associated with abdominal aortic aneurysms in the Belgian population. Annals of the New York Academy of Sciences. 1085: 392-5. PMID 17182961 DOI: 10.1196/Annals.1383.045 |
0.39 |
|
| 2006 |
Lenk GM, Tromp G, Skunca M, Gatalica Z, Berguer R, Kuivaniemi H. Global expression profiles in human normal and aneurysmal abdominal aorta based on two distinct whole genome microarray platforms. Annals of the New York Academy of Sciences. 1085: 360-2. PMID 17182956 DOI: 10.1196/Annals.1383.041 |
0.394 |
|
| 2006 |
Arrington S, Ogata T, Davis PM, Sam AD, Hollier LH, Tromp G, Kuivaniemi H. Aneurysm Outreach Inc., a nonprofit organization, offers community-based, ultrasonography screening for abdominal aortic aneurysms. Annals of the New York Academy of Sciences. 1085: 291-3. PMID 17182945 DOI: 10.1196/Annals.1383.032 |
0.363 |
|
| 2006 |
Kuivaniemi H, Kyo Y, Lenk G, Tromp G. Genome-wide approach to finding abdominal aortic aneurysm susceptibility genes in humans. Annals of the New York Academy of Sciences. 1085: 270-81. PMID 17182943 DOI: 10.1196/Annals.1383.022 |
0.383 |
|
| 2006 |
Wang H, Parry S, Macones G, Sammel MD, Kuivaniemi H, Tromp G, Argyropoulos G, Halder I, Shriver MD, Romero R, Strauss JF. A functional SNP in the promoter of the SERPINH1 gene increases risk of preterm premature rupture of membranes in African Americans. Proceedings of the National Academy of Sciences of the United States of America. 103: 13463-7. PMID 16938879 DOI: 10.1073/Pnas.0603676103 |
0.314 |
|
| 2006 |
Meftah SP, Kuivaniemi H, Tromp G, Kerkeni A, Sfar MT, Ayadi A, Prasad AS. A new mutation in exon 3 of the SCL39A4 gene in a Tunisian family with severe acrodermatitis enteropathica. Nutrition (Burbank, Los Angeles County, Calif.). 22: 1067-70. PMID 16889938 DOI: 10.1016/J.Nut.2006.05.008 |
0.305 |
|
| 2006 |
Ogata T, Gregoire L, Goddard KA, Skunca M, Tromp G, Lancaster WD, Parrado AR, Lu Q, Shibamura H, Sakalihasan N, Limet R, MacKean GL, Arthur C, Sueda T, Kuivaniemi H. Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study. Bmc Medical Genetics. 7: 67. PMID 16879749 DOI: 10.1186/1471-2350-7-67 |
0.409 |
|
| 2006 |
Ogata T, Arrington S, Davis PM, Sam AD, Hollier LH, Tromp G, Kuivaniemi H. Community-based, nonprofit organization-sponsored ultrasonography screening program for abdominal aortic aneurysms is effective at identifying occult aneurysms. Annals of Vascular Surgery. 20: 312-6. PMID 16779511 DOI: 10.1007/S10016-006-9056-5 |
0.323 |
|
| 2006 |
Chowdhury MA, Kuivaniemi H, Romero R, Edwin S, Chaiworapongsa T, Tromp G. Identification of novel functional sequence variants in the gene for peptidase inhibitor 3. Bmc Medical Genetics. 7: 49. PMID 16719916 DOI: 10.1186/1471-2350-7-49 |
0.307 |
|
| 2006 |
Kuivaniemi H, Ogata T. Highlights of the recent literature on abdominal aortic aneurysm research. Annals of Vascular Surgery. 20: 1-4. PMID 16378151 DOI: 10.1007/S10016-005-9167-4 |
0.355 |
|
| 2005 |
Ogata T, MacKean GL, Cole CW, Arthur C, Andreou P, Tromp G, Kuivaniemi H. The lifetime prevalence of abdominal aortic aneurysms among siblings of aneurysm patients is eightfold higher than among siblings of spouses: an analysis of 187 aneurysm families in Nova Scotia, Canada. Journal of Vascular Surgery. 42: 891-7. PMID 16275443 DOI: 10.1016/J.Jvs.2005.08.002 |
0.378 |
|
| 2005 |
Ogata T, Shibamura H, Tromp G, Sinha M, Goddard KA, Sakalihasan N, Limet R, MacKean GL, Arthur C, Sueda T, Land S, Kuivaniemi H. Genetic analysis of polymorphisms in biologically relevant candidate genes in patients with abdominal aortic aneurysms. Journal of Vascular Surgery. 41: 1036-42. PMID 15944607 DOI: 10.1016/J.Jvs.2005.02.020 |
0.412 |
|
| 2005 |
Friel L, Kuivaniemi H, Gomez R, Goddard K, Nien JK, Tromp G, Lu Q, Xu Z, Behnke E, Solari M, Espinoza J, Kim CJ, Chaiworapongsa T, Kim YM, Lenk G, et al. Genetic predisposition for preterm PROM: Results of a large candidate-gene association study of mothers and their offspring American Journal of Obstetrics and Gynecology. 193. DOI: 10.1016/J.Ajog.2005.10.040 |
0.31 |
|
| 2004 |
Wang H, Parry S, Macones G, Sammel MD, Ferrand PE, Kuivaniemi H, Tromp G, Halder I, Shriver MD, Romero R, Strauss JF. Functionally significant SNP MMP8 promoter haplotypes and preterm premature rupture of membranes (PPROM). Human Molecular Genetics. 13: 2659-69. PMID 15367487 DOI: 10.1093/Hmg/Ddh287 |
0.347 |
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| 2004 |
Tromp G, Gatalica Z, Skunca M, Berguer R, Siegel T, Kline RA, Kuivaniemi H. Elevated expression of matrix metalloproteinase-13 in abdominal aortic aneurysms. Annals of Vascular Surgery. 18: 414-20. PMID 15156361 DOI: 10.1007/S10016-004-0050-5 |
0.367 |
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| 2004 |
Shibamura H, Olson JM, van Vlijmen-Van Keulen C, Buxbaum SG, Dudek DM, Tromp G, Ogata T, Skunca M, Sakalihasan N, Pals G, Limet R, MacKean GL, Defawe O, Verloes A, Arthur C, ... ... Kuivaniemi H, et al. Genome scan for familial abdominal aortic aneurysm using sex and family history as covariates suggests genetic heterogeneity and identifies linkage to chromosome 19q13. Circulation. 109: 2103-8. PMID 15096456 DOI: 10.1161/01.Cir.0000127857.77161.A1 |
0.405 |
|
| 2004 |
Kuivaniemi H. Are there genes for aneurysm in the blueprint of the human genome? Annals of Vascular Surgery. 18: 2-3. PMID 15043019 DOI: 10.1007/S10016-003-0110-2 |
0.362 |
|
| 2004 |
Goddard KA, Olson JM, Payami H, van der Voet M, Kuivaniemi H, Tromp G. Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease. Neurogenetics. 5: 121-8. PMID 15034766 DOI: 10.1007/S10048-004-0174-3 |
0.31 |
|
| 2004 |
van der Voet M, Olson JM, Kuivaniemi H, Dudek DM, Skunca M, Ronkainen A, Niemelä M, Jääskeläinen J, Hernesniemi J, Helin K, Leinonen E, Biswas M, Tromp G. Intracranial aneurysms in Finnish families: confirmation of linkage and refinement of the interval to chromosome 19q13.3. American Journal of Human Genetics. 74: 564-71. PMID 14872410 DOI: 10.1086/382285 |
0.304 |
|
| 2004 |
Chowdhury M, Tromp G, Kuivaniemi H, Edwin S, Romero R. Novel functional sequence variants in the promoter of a gene downregulated in preterm prom: A possible genetic basis for the predisposition to membrane rupture? American Journal of Obstetrics and Gynecology. 191. DOI: 10.1016/J.Ajog.2004.09.089 |
0.314 |
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| 2003 |
Wills S, Ronkainen A, van der Voet M, Kuivaniemi H, Helin K, Leinonen E, Frösen J, Niemela M, Jääskeläinen J, Hernesniemi J, Tromp G. Familial intracranial aneurysms: an analysis of 346 multiplex Finnish families. Stroke; a Journal of Cerebral Circulation. 34: 1370-4. PMID 12750547 DOI: 10.1161/01.Str.0000072822.35605.8B |
0.368 |
|
| 2003 |
Kuivaniemi H, Shibamura H, Arthur C, Berguer R, Cole CW, Juvonen T, Kline RA, Limet R, Mackean G, Norrgård O, Pals G, Powell JT, Rainio P, Sakalihasan N, van Vlijmen-van Keulen C, et al. Familial abdominal aortic aneurysms: collection of 233 multiplex families. Journal of Vascular Surgery. 37: 340-5. PMID 12563204 DOI: 10.1067/Mva.2003.71 |
0.363 |
|
| 2002 |
Romero R, Kuivaniemi H, Tromp G, Olson J. The design, execution, and interpretation of genetic association studies to decipher complex diseases. American Journal of Obstetrics and Gynecology. 187: 1299-312. PMID 12439524 DOI: 10.1067/Mob.2002.128319 |
0.332 |
|
| 2002 |
Wang X, Kuivaniemi H, Bonavita G, Mutkus L, Mau U, Blau E, Inohara N, Nunez G, Tromp G, Williams CJ. CARD15 mutations in familial granulomatosis syndromes: a study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy. Arthritis and Rheumatism. 46: 3041-5. PMID 12428248 DOI: 10.1002/Art.10618 |
0.305 |
|
| 2002 |
Ferrand PE, Fujimoto T, Chennathukuzhi V, Parry S, Macones GA, Sammel M, Kuivaniemi H, Romero R, Strauss JF. The CARD15 2936insC mutation and TLR4 896 A>G polymorphism in African Americans and risk of preterm premature rupture of membranes (PPROM). Molecular Human Reproduction. 8: 1031-4. PMID 12397216 DOI: 10.1093/Molehr/8.11.1031 |
0.303 |
|
| 2002 |
Yoon S, Kuivaniemi H, Gatalica Z, Olson JM, Butticè G, Ye S, Norris BA, Malcom GT, Strong JP, Tromp G. MMP13 promoter polymorphism is associated with atherosclerosis in the abdominal aorta of young black males. Matrix Biology : Journal of the International Society For Matrix Biology. 21: 487-98. PMID 12392760 DOI: 10.1016/S0945-053X(02)00053-7 |
0.613 |
|
| 2002 |
Kuivaniemi H, Yoon S, Shibamura H, Skunca M, Vongpunsawad S, Tromp G. Primer-extension preamplified DNA is a reliable template for genotyping. Clinical Chemistry. 48: 1601-4. PMID 12194946 |
0.528 |
|
| 2002 |
Olson JM, Vongpunsawad S, Kuivaniemi H, Ronkainen A, Hernesniemi J, Ryynänen M, Kim LL, Tromp G. Search for intracranial aneurysm susceptibility gene(s) using Finnish families. Bmc Medical Genetics. 3: 7. PMID 12153705 DOI: 10.1186/1471-2350-3-7 |
0.382 |
|
| 2002 |
Ferrand PE, Parry S, Sammel M, Macones GA, Kuivaniemi H, Romero R, Strauss JF. A polymorphism in the matrix metalloproteinase-9 promoter is associated with increased risk of preterm premature rupture of membranes in African Americans. Molecular Human Reproduction. 8: 494-501. PMID 11994547 DOI: 10.1093/Molehr/8.5.494 |
0.314 |
|
| 2002 |
Kuivaniemi H, Yoon S, Shibamura H, Skunca M, Vongpunsawad S, Tromp G. Primer-Extension Preamplified DNA Is a Reliable Template for Genotyping Clinical Chemistry. 48: 1601-1603. DOI: 10.1093/Clinchem/48.9.1601 |
0.598 |
|
| 2001 |
Salkowski A, Tromp G, Greb A, Womble D, Kuivaniemi H. Web-site-based recruitment for research studies on abdominal aortic and intracranial aneurysms Genetic Testing. 5: 307-310. PMID 11960575 DOI: 10.1089/109065701753617435 |
0.388 |
|
| 2001 |
Välkkilä M, Melkoniemi M, Kvist L, Kuivaniemi H, Tromp G, Ala-Kokko L. Genomic organization of the human COL3A1 and COL5A2 genes: COL5A2 has evolved differently than the other minor fibrillar collagen genes Matrix Biology. 20: 357-366. PMID 11566270 DOI: 10.1016/S0945-053X(01)00145-7 |
0.334 |
|
| 2001 |
Asano E, Kuivaniemi H, Mahbubul Huq AHM, Tromp G, Behen M, Rothermel R, Herron J, Chugani DC. A study of novel polymorphisms in the upstream region of vasoactive intestinal peptide receptor type 2 gene in austism Journal of Child Neurology. 16: 357-363. PMID 11392521 DOI: 10.1177/088307380101600509 |
0.325 |
|
| 1999 |
Yoon S, Tromp G, Vongpunsawad S, Ronkainen A, Juvonen T, Kuivaniemi H. Genetic analysis of MMP3, MMP9, and PAI-1 in Finnish patients with abdominal aortic or intracranial aneurysms Biochemical and Biophysical Research Communications. 265: 563-568. PMID 10558909 DOI: 10.1006/Bbrc.1999.1721 |
0.649 |
|
| 1999 |
Wang X, Tromp G, Cole CW, Verloes A, Sakalihasan N, Yoon S, Kuivaniemi H. Analysis of coding sequences for tissue inhibitor of metalloproteinases 1 (TIMP1) and 2 (TIMP2) in patients with aneurysms. Matrix Biology : Journal of the International Society For Matrix Biology. 18: 121-4. PMID 10372551 DOI: 10.1016/S0945-053X(99)00008-6 |
0.66 |
|
| 1998 |
Kuivaniemi H, Marshall A, Ganguly A, Chu ML, Abbott WM, Tromp G. Fibulin-2 exhibits high degree of variability, but no structural changes concordant with abdominal aortic aneurysms European Journal of Human Genetics. 6: 642-646. PMID 9887386 DOI: 10.1038/Sj.Ejhg.5200245 |
0.38 |
|
| 1997 |
Kuivaniemi H, Tromp G, Prockop DJ. Mutations in fibrillar collagens (types I, II, III, and XI), fibril- associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of disease of bone, cartilage, and blood vessels Human Mutation. 9: 300-315. PMID 9101290 DOI: 10.1002/(Sici)1098-1004(1997)9:4<300::Aid-Humu2>3.0.Co;2-9 |
0.304 |
|
| 1997 |
Körkkö J, Kuivaniemi H, Paassilta P, Zhuang J, Tromp G, DePaepe A, Prockop DJ, Ala-Kokko L. Two new recurrent nucleotide mutations in the COL1A1 gene in four patients with osteogenesis imperfecta: About one-fifth are recurrent Human Mutation. 9: 148-156. PMID 9067755 DOI: 10.1002/(Sici)1098-1004(1997)9:2<148::Aid-Humu7>3.0.Co;2-5 |
0.3 |
|
| 1996 |
Anderson DW, Edwards TK, Ricketts MH, Kuivaniemi H, Tromp G, Stolle CA, Deak SB, Boyd CD. Multiple defects in type III collagen synthesis are associated with the pathogenesis of abdominal aortic aneurysms Annals of the New York Academy of Sciences. 800: 216-228. PMID 8958996 DOI: 10.1111/J.1749-6632.1996.Tb33312.X |
0.391 |
|
| 1996 |
Kuivaniemi H, Watton SJ, Price SJ, Zhu Y, Gatalica Z, Tromp G. Candidate genes for abdominal aortic aneurysms Annals of the New York Academy of Sciences. 800: 186-197. PMID 8958993 DOI: 10.1111/J.1749-6632.1996.Tb33309.X |
0.394 |
|
| 1996 |
Zhuang J, Tromp G, Kuivaniemi H, Castells S, Bugge M, Prockop DJ. Direct sequencing of PCR products derived from cDNAs for the proα1 and proα2 chains of type I procollagen as a screening method to detect mutations in patients with osteogenesis imperfecta Human Mutation. 7: 89-99. PMID 8829649 DOI: 10.1002/(Sici)1098-1004(1996)7:2<89::Aid-Humu1>3.0.Co;2-K |
0.306 |
|
| 1995 |
Kuivaniemi H, Tromp G, Bergfeld WF, Kay M, Helm TN. Ehlers-Danlos syndrome type IV: A single base substitution of the last nucleotide of exon 34 in COL3A1 leads to exon skipping Journal of Investigative Dermatology. 105: 352-356. PMID 7665911 DOI: 10.1111/1523-1747.Ep12320704 |
0.343 |
|
| 1995 |
Thakker-Varia S, Anderson DW, Kuivaniemi H, Tromp G, Shin HG, Van Der Rest M, Glorieux FH, Ala-Kokko L, Stolle CA. Aberrant splicing of the type III procollagen mRNA leads to intracellular degradation of the protein in a patient with Ehlers-Danlos type IV Human Mutation. 6: 116-125. PMID 7581395 DOI: 10.1002/Humu.1380060204 |
0.302 |
|
| 1994 |
Ronkainen A, Hernesniemi J, Ryynänen M, Puranen M, Kuivaniemi H. A ten percent prevalence of asymptomatic familial intracranial aneurysms: preliminary report on 110 magnetic resonance angiography studies in members of 21 Finnish familial intracranial aneurysm families. Neurosurgery. 35: 208-213. PMID 7969827 DOI: 10.1227/00006123-199408000-00005 |
0.336 |
|
| 1994 |
Prockop DJ, Kuivaniemi H, Tromp G. Molecular basis of osteogenesis imperfecta and related disorders of bone Clinics in Plastic Surgery. 21: 407-413. PMID 7924138 DOI: 10.1016/S0094-1298(20)31017-8 |
0.313 |
|
| 1994 |
Anderson DW, Tromp G, Kuivaniemi H, Ricketts M, Pope FM, Stolle CA, Boyd CD. A type III procollagen gene mutation in a patient with late onset aneurysms Matrix Biology. 14: 392. DOI: 10.1016/0945-053X(94)90116-3 |
0.365 |
|
| 1993 |
Kuivaniemi H, Prockop DJ, Wu Y, Madhatheri SL, Kleinert C, Earley JJ, Jokinen A, Stolle C, Majamaa K, Myllylä VV, Norrgård O, Schievink WI, Mokri B, Fukawa O, Ter Berg JWM, et al. Exclusion of mutations in the gene for type III collagen (COL3A1) as a common cause of intracranial aneurysms or cervical artery dissections: Results from sequence analysis of the coding sequences of type III collagen from 55 unrelated patients Neurology. 43: 2652-2658. PMID 8255472 DOI: 10.1212/Wnl.43.12.2652 |
0.376 |
|
| 1993 |
Narcisi P, Wu Y, Tromp G, Earley JJ, Richards AJ, Pope FM, Kuivaniemi H. Single base mutation that substitutes glutamic acid for glycine 1021 in the COL3A1 gene and causes Ehlers-Danlos syndrome type IV American Journal of Medical Genetics. 46: 278-283. PMID 8098182 DOI: 10.1002/Ajmg.1320460308 |
0.316 |
|
| 1993 |
Zhuang J, Tromp G, Kuivaniemi H, Nakayasu K, Prockop DJ. Deletion of 19 base pairs in intron 13 of the gene for the proα2(I) chain of type-I procollagen (COL1A2) causes exon skipping in a proband with type-I osteogenesis imperfecta Human Genetics. 91: 210-216. PMID 7916744 DOI: 10.1007/Bf00218258 |
0.301 |
|
| 1992 |
Tromp G, Kuivaniemi H. DNA sequencing as a method to identify mutations in patients with familial forms of aneurysms Journal of Vascular Surgery. 15: 928-930. PMID 1578572 DOI: 10.1016/0741-5214(92)90756-X |
0.34 |
|
| 1992 |
Mays PK, Tromp G, Kuivaniemi H, Ryynanen M, Prockop DJ. A 15 base-pair AT-rich variable number tandem repeat in the type III procollagen (COL3A1) as an informative marker for 2q31-2q32.3 Matrix. 12: 44-49. PMID 1560789 DOI: 10.1016/S0934-8832(11)80103-4 |
0.322 |
|
| 1991 |
Kuivaniemi H, Tromp G, Prockop DJ. Mutations in collagen genes: Causes of rare and some common diseases in humans Faseb Journal. 5: 2052-2060. PMID 2010058 DOI: 10.1096/Fasebj.5.7.2010058 |
0.338 |
|
| 1991 |
Kuivaniemi H, Tromp G, Prockop DJ. Genetic causes of aortic aneurysms: Unlearning at least part of what the textbooks say Journal of Clinical Investigation. 88: 1441-1444. PMID 1939638 DOI: 10.1172/Jci115452 |
0.385 |
|
| 1990 |
Kontusaari S, Tromp G, Kuivaniemi H, Romanic AM, Prockop DJ. A mutation in the gene for type III procollagen (COL3A1) in a family with aortic aneurysms Journal of Clinical Investigation. 86: 1465-1473. PMID 2243125 DOI: 10.1172/Jci114863 |
0.401 |
|
| 1990 |
Kontusaari S, Kuivaniemi H, Tromp G, Grimwood R, Prockop DJ. A single base mutation in type III procollagen that converts the codon for glycine 619 to arginine in a family with familial aneurysms and mild bleeding tendencies Annals of the New York Academy of Sciences. 580: 556-557. DOI: 10.1111/J.1749-6632.1990.Tb17990.X |
0.318 |
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