Gerard Tromp - Publications

Affiliations: 
Molecular Biology and Genetics Wayne State University, Detroit, MI, United States 
Area:
Genetics, Molecular Biology

172 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Verma SS, Cooke Bailey JN, Lucas A, Bradford Y, Linneman JG, Hauser MA, Pasquale LR, Peissig PL, Brilliant MH, McCarty CA, Haines JL, Wiggs JL, Vrabec TR, Tromp G, Ritchie MD, et al. Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium. Plos Genetics. 12: e1006186. PMID 27623284 DOI: 10.1371/journal.pgen.1006186  0.64
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, ... ... Tromp G, 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  0.64
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  0.64
2016 Simonti CN, Vernot B, Bastarache L, Bottinger E, Carrell DS, Chisholm RL, Crosslin DR, Hebbring SJ, Jarvik GP, Kullo IJ, Li R, Pathak J, Ritchie MD, Roden DM, Verma SS, ... Tromp G, et al. The phenotypic legacy of admixture between modern humans and Neandertals. Science (New York, N.Y.). 351: 737-41. PMID 26912863 DOI: 10.1126/science.aad2149  0.64
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  0.64
2015 Mo H, Thompson WK, Rasmussen LV, Pacheco JA, Jiang G, Kiefer R, Zhu Q, Xu J, Montague E, Carrell DS, Lingren T, Mentch FD, Ni Y, Wehbe FH, Peissig PL, ... Tromp G, et al. Desiderata for computable representations of electronic health records-driven phenotype algorithms. Journal of the American Medical Informatics Association : Jamia. PMID 26342218 DOI: 10.1093/jamia/ocv112  0.64
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  0.64
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, ... ... Tromp G, 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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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, ... ... Tromp G, 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  0.64
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  0.64
2015 Crosslin DR, Robertson PD, Carrell DS, Gordon AS, Hanna DS, Burt A, Fullerton SM, Scrol A, Ralston J, Leppig K, Hartzler A, Baldwin E, Andrade Md, Kullo IJ, Tromp G, et al. Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network Genome Medicine. DOI: 10.1186/s13073-015-0181-z  0.64
2015 Freitag D, Butterworth AS, Willeit P, Howson JMM, Burgess S, Kaptoge S, Young R, Ho WK, Wood AM, Sweeting M, Spackman S, Staley JR, Ramond A, Harshfield E, Nielsen SF, ... ... Tromp G, et al. Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: A Mendelian randomisation analysis The Lancet Diabetes and Endocrinology. 3: 243-253. DOI: 10.1016/S2213-8587(15)00034-0  0.64
2015 Kuivaniemi H, Ryer EJ, Yoon HR, Elmore JR, Tromp G. Genetic risk factors for abdominal aortic aneurysms (AAA) Horizons in World Cardiovascular Research. 7: 1-31.  0.64
2014 Verma SS, de Andrade M, Tromp G, Kuivaniemi H, Pugh E, Namjou-Khales B, Mukherjee S, Jarvik GP, Kottyan LC, Burt A, Bradford Y, Armstrong GD, Derr K, Crawford DC, Haines JL, et al. Imputation and quality control steps for combining multiple genome-wide datasets. Frontiers in Genetics. 5: 370. PMID 25566314 DOI: 10.3389/fgene.2014.00370  0.64
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  0.64
2014 Crosslin DR, Tromp G, Burt A, Kim DS, Verma SS, Lucas AM, Bradford Y, Crawford DC, Armasu SM, Heit JA, Hayes MG, Kuivaniemi H, Ritchie MD, Jarvik GP, de Andrade M, et al. Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records. Frontiers in Genetics. 5: 352. PMID 25414722 DOI: 10.3389/fgene.2014.00352  0.64
2014 Barrie ES, Weinshenker D, Verma A, Pendergrass SA, Lange LA, Ritchie MD, Wilson JG, Kuivaniemi H, Tromp G, Carey DJ, Gerhard GS, Brilliant MH, Hebbring SJ, Cubells JF, Pinsonneault JK, et al. Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activity. Circulation Research. 115: 1017-25. PMID 25326128 DOI: 10.1161/CIRCRESAHA.116.304398  0.64
2014 Cronin RM, Field JR, Bradford Y, Shaffer CM, Carroll RJ, Mosley JD, Bastarache L, Edwards TL, Hebbring SJ, Lin S, Hindorff LA, Crane PK, Pendergrass SA, Ritchie MD, Crawford DC, ... ... Tromp G, et al. Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index. Frontiers in Genetics. 5: 250. PMID 25177340 DOI: 10.3389/fgene.2014.00250  0.64
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  0.64
2014 Crawford DC, Crosslin DR, Tromp G, Kullo IJ, Kuivaniemi H, Hayes MG, Denny JC, Bush WS, Haines JL, Roden DM, McCarty CA, Jarvik GP, Ritchie MD. eMERGEing progress in genomics-the first seven years. Frontiers in Genetics. 5: 184. PMID 24987407 DOI: 10.3389/fgene.2014.00184  0.64
2014 Rasmussen LV, Thompson WK, Pacheco JA, Kho AN, Carrell DS, Pathak J, Peissig PL, Tromp G, Denny JC, Starren JB. Design patterns for the development of electronic health record-driven phenotype extraction algorithms. Journal of Biomedical Informatics. 51: 280-6. PMID 24960203 DOI: 10.1016/j.jbi.2014.06.007  0.64
2014 Schrodi SJ, Mukherjee S, Shan Y, Tromp G, Sninsky JJ, Callear AP, Carter TC, Ye Z, Haines JL, Brilliant MH, Crane PK, Smelser DT, Elston RC, Weeks DE. Genetic-based prediction of disease traits: prediction is very difficult, especially about the future. Frontiers in Genetics. 5: 162. PMID 24917882 DOI: 10.3389/fgene.2014.00162  0.64
2014 Muthalagu A, Pacheco JA, Aufox S, Peissig PL, Fuehrer JT, Tromp G, Kho AN, Rasmussen-Torvik LJ. A rigorous algorithm to detect and clean inaccurate adult height records within EHR systems Applied Clinical Informatics. 5: 118-126. PMID 24734128 DOI: 10.4338/ACI-2013-09-RA-0074  0.64
2014 Patel ZH, Kottyan LC, Lazaro S, Williams MS, Ledbetter DH, Tromp H, Rupert A, Kohram M, Wagner M, Husami A, Qian Y, Valencia CA, Zhang K, Hostetter MK, Harley JB, et al. The struggle to find reliable results in exome sequencing data: filtering out Mendelian errors. Frontiers in Genetics. 5: 16. PMID 24575121 DOI: 10.3389/fgene.2014.00016  0.64
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  0.64
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, ... ... Tromp G, 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  0.64
2013 Betoni JS, Derr K, Pahl MC, Rogers L, Muller CL, Packard RE, Carey DJ, Kuivaniemi H, Tromp G. MicroRNA analysis in placentas from patients with preeclampsia: comparison of new and published results. Hypertension in Pregnancy. 32: 321-39. PMID 23844600 DOI: 10.3109/10641955.2013.807819  0.64
2013 Gottesman O, Kuivaniemi H, Tromp G, Faucett WA, Li R, Manolio TA, Sanderson SC, Kannry J, Zinberg R, Basford MA, Brilliant M, Carey DJ, Chisholm RL, Chute CG, Connolly JJ, et al. The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 761-71. PMID 23743551 DOI: 10.1038/gim.2013.72  0.64
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, 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  0.64
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, ... ... Tromp G, 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  0.64
2012 Gaffney CJ, Oka T, Mazack V, Hilman D, Gat U, Muramatsu T, Inazawa J, Golden A, Carey DJ, Farooq A, Tromp G, Sudol M. Identification, basic characterization and evolutionary analysis of differentially spliced mRNA isoforms of human YAP1 gene. Gene. 509: 215-22. PMID 22939869 DOI: 10.1016/j.gene.2012.08.025  0.64
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, ... ... Tromp G, 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  0.64
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  0.64
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  0.64
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, ... ... Tromp G, 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  0.64
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, ... ... Tromp G, 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  0.64
2011 Kurki MI, Häkkinen SK, Frösen J, Tulamo R, von und zu Fraunberg M, Wong G, Tromp G, Niemelä M, Hernesniemi J, Jääskeläinen JE, Ylä-Herttuala S. Upregulated signaling pathways in ruptured human saccular intracranial aneurysm wall: an emerging regulative role of Toll-like receptor signaling and nuclear factor-κB, hypoxia-inducible factor-1A, and ETS transcription factors. Neurosurgery. 68: 1667-75; discussion . PMID 21336216 DOI: 10.1227/NEU.0b013e318210f001  0.64
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  0.64
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  0.64
2011 Edwards DR, Romero R, Kusanovic JP, Hassan SS, Mazaki-Tovi S, Vaisbuch E, Kim CJ, Erez O, Chaiworapongsa T, Pearce BD, Bartlett J, Friel LA, Salisbury BA, Anant MK, Vovis GF, ... ... Tromp G, et al. Polymorphisms in maternal and fetal genes encoding for proteins involved in extracellular matrix metabolism alter the risk for small-for-gestational-age. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 24: 362-80. PMID 20617897 DOI: 10.3109/14767058.2010.497572  0.64
2010 Romero R, Friel LA, Velez Edwards DR, Kusanovic JP, Hassan SS, Mazaki-Tovi S, Vaisbuch E, Kim CJ, Erez O, Chaiworapongsa T, Pearce BD, Bartlett J, Salisbury BA, Anant MK, Vovis GF, ... ... Tromp G, et al. A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM). American Journal of Obstetrics and Gynecology. 203: 361.e1-361.e30. PMID 20673868 DOI: 10.1016/j.ajog.2010.05.026  0.64
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, ... ... Tromp G, 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  0.64
2010 Romero R, Velez Edwards DR, Kusanovic JP, Hassan SS, Mazaki-Tovi S, Vaisbuch E, Kim CJ, Chaiworapongsa T, Pearce BD, Friel LA, Bartlett J, Anant MK, Salisbury BA, Vovis GF, Lee MS, ... ... Tromp G, et al. Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes. American Journal of Obstetrics and Gynecology. 202: 431.e1-34. PMID 20452482 DOI: 10.1016/j.ajog.2010.03.026  0.64
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  0.64
2010 Huttunen T, von und zu Fraunberg M, Frösen J, Lehecka M, Tromp G, Helin K, Koivisto T, Rinne J, Ronkainen A, Hernesniemi J, Jääskeläinen JE. Saccular intracranial aneurysm disease: distribution of site, size, and age suggests different etiologies for aneurysm formation and rupture in 316 familial and 1454 sporadic eastern Finnish patients. Neurosurgery. 66: 631-8; discussion 63. PMID 20190670 DOI: 10.1227/01.NEU.0000367634.89384.4B  0.64
2009 Mittal P, Romero R, Mazaki-Tovi S, Tromp G, Tarca AL, Kim YM, Chaiworapongsa T, Kusanovic JP, Erez O, Than NG, Hassan SS. Fetal membranes as an interface between inflammation and metabolism: increased aquaporin 9 expression in the presence of spontaneous labor at term and chorioamnionitis. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 22: 1167-75. PMID 19916714 DOI: 10.3109/14767050903019692  0.64
2009 Erez O, Romero R, Tarca AL, Chaiworapongsa T, Kim YM, Than NG, Vaisbuch E, Draghici S, Tromp G. Differential expression pattern of genes encoding for anti-microbial peptides in the fetal membranes of patients with spontaneous preterm labor and intact membranes and those with preterm prelabor rupture of the membranes. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 22: 1103-15. PMID 19916708 DOI: 10.3109/14767050902994796  0.64
2009 Than NG, Romero R, Tarca AL, Draghici S, Erez O, Chaiworapongsa T, Kim YM, Kim SK, Vaisbuch E, Tromp G. Mitochondrial manganese superoxide dismutase mRNA expression in human chorioamniotic membranes and its association with labor, inflammation, and infection. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 22: 1000-13. PMID 19900038 DOI: 10.3109/14767050903019676  0.64
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  0.64
2009 Rosner K, Mehregan DR, Moussai D, Abrams J, Tromp G, Mehregan DA. WT1 marker is not sufficient for distinguishing between melanoma and melanocytic nevi. Journal of Cutaneous Pathology. 36: 1077-82. PMID 19615003 DOI: 10.1111/j.1600-0560.2009.01224.x  0.64
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.2009.01.041  0.64
2009 Elmore JR, Obmann MA, Kuivaniemi H, Tromp G, Gerhard GS, Franklin DP, Carey DJ, Boddy AM. Reply Journal of Vascular Surgery. 50: 1247. DOI: 10.1016/j.jvs.2009.07.100  0.64
2008 Tang Z, Yu M, Miller F, Berk RS, Tromp G, Kosir MA. Increased invasion through basement membrane by CXCL7-transfected breast cells. American Journal of Surgery. 196: 690-6. PMID 18954601 DOI: 10.1016/j.amjsurg.2008.08.001  0.64
2008 Liang J, Song W, Tromp G, Kolattukudy PE, Fu M. Genome-wide survey and expression profiling of CCCH-zinc finger family reveals a functional module in macrophage activation Plos One. 3. PMID 18682727 DOI: 10.1371/journal.pone.0002880  0.4
2008 Kazzi SN, Tromp G, Quasney MW, Buhimschi IA. Haplotypes of tumor necrosis factor gene and tracheal aspirate fluid levels of tumor necrosis factor-alpha in preterm infants. Pediatric Research. 64: 165-70. PMID 18645461 DOI: 10.1203/PDR.0b013e31817758f4  0.64
2008 Parimi N, Tromp G, Kuivaniemi H, Nien JK, Gomez R, Romero R, Goddard KA. Analytical approaches to detect maternal/fetal genotype incompatibilities that increase risk of pre-eclampsia. Bmc Medical Genetics. 9: 60. PMID 18598365 DOI: 10.1186/1471-2350-9-60  0.64
2008 Haddad R, Romero R, Gould BR, Tromp G, Gotsch F, Edwin SS, Zingg HH. Angiogenesis gene expression in mouse uterus during the common pathway of parturition. American Journal of Obstetrics and Gynecology. 198: 539.e1-8. PMID 18455529 DOI: 10.1016/j.ajog.2007.11.021  0.64
2008 Wang H, Sammel MD, Tromp G, Gotsch F, Halder I, Shriver MD, Romero R, Strauss JF. A 12-bp deletion in the 5'-flanking region of the SERPINH1 gene affects promoter activity and protects against preterm premature rupture of membranes in African Americans. Human Mutation. 29: 332. PMID 18205191 DOI: 10.1002/humu.9522  0.64
2008 Liang J, Wang J, Azfer A, Song W, Tromp G, Kolattukudy PE, Fu M. A novel CCCH-zinc finger protein family regulates proinflammatory activation of macrophages Journal of Biological Chemistry. 283: 6337-6346. PMID 18178554 DOI: 10.1074/jbc.M707861200  0.4
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  0.64
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, ... ... Tromp G, 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  0.64
2008 Romero R, Espinoza J, Gotsch F, Kusanovic JP, Friel LA, Erex O, Mazaki-Tovi S, Than NG, Hassan S, Tromp G. The use of high-dimensional biology (genomics, transcriptomics, proteomics, and metabolomics) to understand the preterm parturition syndrome (BJOG: An International Journal of Obstetrics and Gynaecology 113, SUPPL. 3, (118-135)) Bjog: An International Journal of Obstetrics and Gynaecology. 115: 675. DOI: 10.1111/j.1471-0528.2008.01712_2.x  0.64
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 146A, (271-283)) American Journal of Medical Genetics, Part A. 146: 952-964. DOI: 10.1002/ajmg.a.32328  0.64
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  0.64
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  0.64
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, ... Tromp G, 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  0.64
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  0.64
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, 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  0.64
2006 Romero R, Espinoza J, Gotsch F, Kusanovic JP, Friel LA, Erez O, Mazaki-Tovi S, Than NG, Hassan S, Tromp G. The use of high-dimensional biology (genomics, transcriptomics, proteomics, and metabolomics) to understand the preterm parturition syndrome. Bjog : An International Journal of Obstetrics and Gynaecology. 113: 118-35. PMID 17206980 DOI: 10.1111/j.1471-0528.2006.01150.x  0.64
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  0.64
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  0.64
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  0.64
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  0.64
2006 Haddad R, Gould BR, Romero R, Tromp G, Farookhi R, Edwin SS, Kim MR, Zingg HH. Uterine transcriptomes of bacteria-induced and ovariectomy-induced preterm labor in mice are characterized by differential expression of arachidonate metabolism genes. American Journal of Obstetrics and Gynecology. 195: 822-8. PMID 16949419 DOI: 10.1016/j.ajog.2006.06.053  0.64
2006 Hassan SS, Romero R, Haddad R, Hendler I, Khalek N, Tromp G, Diamond MP, Sorokin Y, Malone J. The transcriptome of the uterine cervix before and after spontaneous term parturition. American Journal of Obstetrics and Gynecology. 195: 778-86. PMID 16949412 DOI: 10.1016/j.ajog.2006.06.021  0.64
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  0.64
2006 Haddad R, Tromp G, Kuivaniemi H, Chaiworapongsa T, Kim YM, Mazor M, Romero R. Human spontaneous labor without histologic chorioamnionitis is characterized by an acute inflammation gene expression signature. American Journal of Obstetrics and Gynecology. 195: 394.e1-24. PMID 16890549 DOI: 10.1016/j.ajog.2005.08.057  0.64
2006 Romero R, Tromp G. High-dimensional biology in obstetrics and gynecology: functional genomics in microarray studies. American Journal of Obstetrics and Gynecology. 195: 360-3. PMID 16890547 DOI: 10.1016/j.ajog.2006.06.077  0.64
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  0.64
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  0.64
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  0.64
2006 Romero R, Tarca AL, Tromp G. Insights into the physiology of childbirth using transcriptomics. Plos Medicine. 3: e276. PMID 16752954 DOI: 10.1371/journal.pmed.0030276  0.64
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  0.64
2006 Chatterjee M, Mohapatra S, Ionan A, Bawa G, Ali-Fehmi R, Wang X, Nowak J, Ye B, Nahhas FA, Lu K, Witkin SS, Fishman D, Munkarah A, Morris R, Levin NK, ... ... Tromp G, et al. Diagnostic markers of ovarian cancer by high-throughput antigen cloning and detection on arrays. Cancer Research. 66: 1181-90. PMID 16424057 DOI: 10.1158/0008-5472.CAN-04-2962  0.64
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  0.64
2005 Kim GJ, Romero R, Kuivaniemi H, Tromp G, Haddad R, Kim YM, Kim MR, Nien JK, Hong JS, Espinoza J, Santolaya J, Yoon BH, Mazor M, Kim CJ. Expression of bone morphogenetic protein 2 in normal spontaneous labor at term, preterm labor, and preterm premature rupture of membranes. American Journal of Obstetrics and Gynecology. 193: 1137-43. PMID 16157126 DOI: 10.1016/j.ajog.2005.06.032  0.64
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  0.64
2005 Gatalica Z, Velagaleti G, Kuivaniemi H, Tromp G, Palazzo J, Graves KM, Guigneaux M, Wood T, Sinha M, Luxon B. Gene expression profile of an adenomyoepithelioma of the breast with a reciprocal translocation involving chromosomes 8 and 16. Cancer Genetics and Cytogenetics. 156: 14-22. PMID 15588851 DOI: 10.1016/j.cancergencyto.2004.04.024  0.64
2004 Kim YM, Romero R, Chaiworapongsa T, Kim GJ, Kim MR, Kuivaniemi H, Tromp G, Espinoza J, Bujold E, Abrahams VM, Mor G. Toll-like receptor-2 and -4 in the chorioamniotic membranes in spontaneous labor at term and in preterm parturition that are associated with chorioamnionitis. American Journal of Obstetrics and Gynecology. 191: 1346-55. PMID 15507964 DOI: 10.1016/j.ajog.2004.07.009  0.64
2004 Tromp G, Kuivaniemi H, Romero R, Chaiworapongsa T, Kim YM, Kim MR, Maymon E, Edwin S. Genome-wide expression profiling of fetal membranes reveals a deficient expression of proteinase inhibitor 3 in premature rupture of membranes. American Journal of Obstetrics and Gynecology. 191: 1331-8. PMID 15507962 DOI: 10.1016/j.ajog.2004.07.010  0.64
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  0.64
2004 Romero R, Chaiworapongsa T, Kuivaniemi H, Tromp G. Bacterial vaginosis, the inflammatory response and the risk of preterm birth: a role for genetic epidemiology in the prevention of preterm birth. American Journal of Obstetrics and Gynecology. 190: 1509-19. PMID 15284723 DOI: 10.1016/j.ajog.2004.01.002  0.64
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  0.64
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, 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  0.64
2004 Tanabe T, Chamaillard M, Ogura Y, Zhu L, Qiu S, Masumoto J, Ghosh P, Moran A, Predergast MM, Tromp G, Williams CJ, Inohara N, Núñez G. Regulatory regions and critical residues of NOD2 involved in muramyl dipeptide recognition. The Embo Journal. 23: 1587-97. PMID 15044951 DOI: 10.1038/sj.emboj.7600175  0.64
2004 Theendakara V, Tromp G, Kuivaniemi H, White PS, Panchal S, Cox J, Winters RS, Riebeling P, Tost F, Hoeltzenbein M, Tervo TM, Henn W, Denniger E, Krause M, Koksal M, et al. Fine mapping of the Schnyder's crystalline corneal dystrophy locus. Human Genetics. 114: 594-600. PMID 15034782 DOI: 10.1007/s00439-004-1110-1  0.64
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  0.64
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  0.64
2003 Zhong J, Zhang H, Stanyon CA, Tromp G, Finley RL. A strategy for constructing large protein interaction maps using the yeast two-hybrid system: regulated expression arrays and two-phase mating. Genome Research. 13: 2691-9. PMID 14613974 DOI: 10.1101/gr.1134603  0.64
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  0.64
2003 Kuivaniemi H, Shibamura H, Arthur C, Berguer R, Cole CW, Juvonen T, Kline RA, Limet R, Mackean G, NorrgÃ¥rd O, Pals G, Powell JT, Rainio P, Sakalihasan N, van Vlijmen-van Keulen C, ... ... Tromp G, 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  0.64
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  0.64
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  0.64
2002 Wang X, Kuivaniemi H, Bonavita G, Williams CJ, Tromp G. High-resolution physical map for chromosome 16q12.1-q13, the Blau syndrome locus. Bmc Genomics. 3: 24. PMID 12186634 DOI: 10.1186/1471-2164-3-24  0.64
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  0.64
2002 Romero R, Kuivaniemi H, Tromp G. Functional genomics and proteomics in term and preterm parturition. The Journal of Clinical Endocrinology and Metabolism. 87: 2431-4. PMID 12050194 DOI: 10.1210/jcem.87.6.8689  0.64
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  0.64
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  0.64
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  0.64
2001 Virgin JB, Bailey JP, Hasteh F, Neville J, Cole A, Tromp G. Crossing over is rarely associated with mitotic intragenic recombination in Schizosaccharomyces pombe Genetics. 157: 63-77. PMID 11139492  0.64
2000 Kosir MA, Quinn CC, Wang W, Tromp G. Matrix glycosaminoglycans in the growth phase of fibroblasts: more of the story in wound healing. The Journal of Surgical Research. 92: 45-52. PMID 10864481 DOI: 10.1006/jsre.2000.5840  0.64
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  0.64
1999 Papponen H, Toppinen T, Baumann P, Myllylä V, Leisti J, Kuivaniemi H, Tromp G, Myllylä R. Founder mutations and the high prevalence of myotonia congenita in northern Finland Neurology. 53: 297-302. PMID 10430417  0.64
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  0.64
1999 Kosir MA, Wang W, Zukowski KL, Tromp G, Barber J. Degradation of basement membrane by prostate tumor heparanase Journal of Surgical Research. 81: 42-47. PMID 9889056 DOI: 10.1006/jsre.1998.5519  0.64
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  0.64
1998 Devoto M, Shimoya K, Caminis J, Ott J, Tenenhouse A, Whyte MP, Sereda L, Hall S, Considine E, Williams CJ, Tromp G, Kuivaniemi H, Ala-Kokko L, Prockop DJ, Spotila LD. First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q. European Journal of Human Genetics : Ejhg. 6: 151-7. PMID 9781060 DOI: 10.1038/sj.ejhg.5200169  0.64
1997 Zafarullah K, Sieron AL, Fertala A, Tromp G, Kuivaniemi H, Prockop DJ. A recombinant homotrimer of type I procollagen that lacks the central two D-periods. The thermal stability of the triple helix is decreased by 2 to 4°C Matrix Biology. 16: 245-253. PMID 9501325 DOI: 10.1016/S0945-053X(97)90013-5  0.64
1997 Zafarullah K, Brown EM, Kuivaniemi H, Tromp G, Sieron AL, Fertala A, Prockop DJ. Synthesis and conformational properties of a recombinant C-propeptide of human type III procollagen Matrix Biology. 16: 201-209. PMID 9402010 DOI: 10.1016/S0945-053X(97)90009-3  0.64
1997 Linn FH, Bromberg JE, Rinkel GJ, Algra A, van Gijn J. Familial intracranial aneurysms. Lancet. 349: 1477-8. PMID 9164343  0.64
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  0.64
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  0.64
1997 Anderson DW, Thakker-Varia S, Tromp G, Kuivaniemi H, Stolle CA. A glycine (415)-to-serine substitution results in impaired secretion and decreased thermal stability of type III procollagen in a patient with Ehlers- Danlos syndrome type IV Human Mutation. 9: 62-63. PMID 8990011 DOI: 10.1002/(SICI)1098-1004(1997)9:1<62::AID-HUMU11>3.0.CO;2-N  0.64
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  0.64
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  0.64
1996 Tromp G, Kuivaniemi H, Raphael S, Ala-Kokko L, Christiano A, Considine E, Dhulipala R, Hyland J, Jokinen A, Kivirikko S, Korn R, Madhatheri S, McCarron S, Pulkkinen L, Punnett H, et al. Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16. American Journal of Human Genetics. 59: 1097-107. PMID 8900239  0.64
1996 Jaakkola P, Kuivaniemi H, Partanen K, Tromp G, Liljeström B, Ryynänen M. Familial Abdominal Aortic Aneurysms: Screening of 71 Families European Journal of Surgery. 162: 611-617. PMID 8891618  0.64
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  0.64
1996 Zhuang J, Tromp G, Kuivaniemi H, Castells S, Prockop DJ. Substitution of arginine for glycine at position 154 of the α1 chain of type I collagen in a variant of osteogenesis imperfecta: Comparison to previous cases with the same mutation American Journal of Medical Genetics. 61: 111-116. PMID 8669434 DOI: 10.1002/(SICI)1096-8628(19960111)61:2<111::AID-AJMG1>3.0.CO;2-#  0.64
1996 Kemppainen R, Hämäläinen ER, Kuivaniemi H, Tromp G, Pihlajaniemi T, Kivirikko KI. Expression of mRNAs for lysyl oxidase and type III procollagen in cultured fibroblasts from patients with the Menkes and occipital horn syndromes as determined by quantitative polymerase chain reaction Archives of Biochemistry and Biophysics. 328: 101-106. PMID 8638917 DOI: 10.1006/abbi.1996.0148  0.64
1996 Ronkainen A, Hernesniemi J, Kuivaniemi H, Tromp G, Obuchowski NA. Screening for aneurysms [1] Journal of Neurosurgery. 84: 534-536. PMID 8609572  0.64
1996 Kuivaniemi H, Shikata H, Utsumi N, Tromp G. Mutations in type III procollagen gene as causes of heritable disorders Connective Tissue. 28: 205-213.  0.64
1995 Ronkainen A, Hernesniemi J, Tromp G. Special features of familial intracranial aneurysms: Report of 215 familial aneurysms Neurosurgery. 37: 43-47. PMID 8587689  0.64
1995 Tromp G, De Paepe A, Nuytinck L, Madhatheri S, Kuivaniemi H. Substitution of valine for g793 in type III procollagen in Ehlers-Danlos syndrome type IV Human Mutation. 5: 179-181. PMID 7749417  0.64
1995 Shikata H, Utsumi N, Kuivaniemi H, Tromp G. DNA-based diagnostics in the study of heritable and acquired disorders Journal of Laboratory and Clinical Medicine. 125: 421-432. PMID 7706896  0.64
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  0.64
1995 Hämäläinen ER, Kemppainen R, Kuivaniemi H, Tromp G, Vaheri A, Pihlajaniemi T, Kivirikko KI. Quantitative polymerase chain reaction of lysyl oxidase mRNA in malignantly transformed human cell lines demonstrates that their low lysyl oxidase activity is due to low quantities of its mRNA and low levels of transcription of the respective gene Journal of Biological Chemistry. 270: 21590-21593. PMID 7665572  0.64
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  0.64
1994 Earley JJ, Kuivaniemi H, Prockop DJ, Tromp G. Robotic automation of dideoxyribonucleotide sequencing reactions Biotechniques. 17: 156-158+160+162. PMID 7946299  0.64
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  0.64
1994 Madhatheri SL, Tromp G, Gustavson KH, Kulvanlemi H. Substitution of glutamic acid for glycine 589 in the triple-helical domain of type III procollagen (COL3A1) in a family with variable phenotype of the ehlers-danlos syndrome type IV Human Molecular Genetics. 3: 511-512. PMID 7912131 DOI: 10.1093/hmg/3.3.511  0.64
1993 Tromp G, Wu Y, Prockop DJ, Madhatheri SL, Kleinert C, Earley JJ, Zhuang J, Norrgård O, Darling RC, Abbott WM, Cole CW, Jaakkola P, Ryynänen M, Pearce WH, Yao JST, et al. Sequencing of cDNA from 50 unrelated patients reveals that mutations in the triple-helical domain of type III procollagen are an infrequent cause of aortic aneurysms Journal of Clinical Investigation. 91: 2539-2545. PMID 8514866  0.64
1993 Wu Y, Kuivaniemi H, Tromp G, Strobel D, Romanic AM, Prockop DJ. Temperature sensitivity of aberrant RNA splicing with a mutation in the G+5 position of intron 37 of the gene for type III procollagen from a patient with Ehlers-Danlos syndrome type IV Human Mutation. 2: 28-36. PMID 8477261  0.64
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, ... ... Tromp G, 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  0.64
1993 Earley JJ, Kuivaniemi H, Prockop DJ, Tromp G. Efficient DNA sequencing on microtiter plates using dried reagents and bst DNA polymerase Mitochondrial Dna. 4: 79-85. PMID 8173079 DOI: 10.3109/10425179309020146  0.64
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  0.64
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  0.64
1992 Strobel D, Tsuneyoshi T, Kuivaniemi H, Tromp G, Spotila LD, Baldwin CT, Constantinou CD, Ganguly A, Sereda L, Sokolov BP. Three new polymorphisms at the COL1A2 locus. Matrix (Stuttgart, Germany). 12: 87-91. PMID 1603040  0.64
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  0.64
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  0.64
1992 Kontusaari S, Tromp G, Kuivaniemi H, Stolle C, Pope FM, Prockop DJ. Substitution of aspartate for glycine 1018 in the type III procollagen (COL3AI) gene causes type IV Ehlers-Danlos syndrome: The mutated allele is present in most blood leukocytes of the asymptomatic and mosaic mother American Journal of Human Genetics. 51: 497-507. PMID 1496983  0.64
1991 Tromp G, Kleinert C, Kuivaniemi H, Prockop DJ. C to T polymorphism in exon 33 of the COL3A1 gene Nucleic Acids Research. 19: 681. PMID 2011540 DOI: 10.1093/nar/19.3.681  0.64
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  0.64
1991 Vasan NS, Kuivaniemi H, Vogel BE, Minor RR, Wootton JAM, Tromp G, Weksberg R, Prockop DJ. A mutation in the proα2(I) Gene (COLIA2) for type I procollagen in Ehlers-Danlos syndrome type VII: Evidence suggesting that skipping of exon 6 in RNA splicing may be a common cause of the phenotype American Journal of Human Genetics. 48: 305-317. PMID 1990839  0.64
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  0.64
1991 Tromp G, Christiano A, Goldstein N, Indik Z, Boyd C, Rosenbloom J, Deak S, Prockop D, Kuivaniemi H. A to G polymorphism in ELN gene Nucleic Acids Research. 19: 4314. PMID 1871001 DOI: 10.1093/nar/19.15.4314-a  0.64
1991 Sokolov BP, Prytkov AN, Tromp G, Knowlton RG, Prockop DJ. Exclusion of COL1A1, COL1A2, and COL3A1 genes as candidate genes for Ehlers-Danlos syndrome type I in one large family. Human Genetics. 88: 125-9. PMID 1684560 DOI: 10.1007/BF00206058  0.64
1991 Kuivaniemi H, Tromp G. Are arterial aneurysms hereditary? | Periytyvätkö valtimoaneurysmat? Duodecim. 107: 1629-1632. PMID 1365930  0.64
1990 Kuivaniemi H, Kontusaari S, Tromp G, Zhao M, Sabol C, Prockop DJ. Identical G+1 to a mutations in three different introns of the type III procollagen gene (COL3A1) produce different patterns of RNA splicing in three variants of Ehlers-Danlos syndrome IV: An explanation for exon skipping with some mutations and not others Journal of Biological Chemistry. 265: 12067-12074. PMID 2365710  0.64
1990 Kontusaari S, Tromp G, Kuivaniemi H, Ladda RL, Prockop DJ. Inheritance of an RNA splicing mutation (G+I IVS20) in the type III procollagen gene (COL3AI) in a family having aortic aneurysms and easy bruisability: Phenotypic overlap between familial arterial aneurysms and Ehlers-Danlos syndrome type IV American Journal of Human Genetics. 47: 112-120. PMID 2349939  0.64
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  0.64
1990 Zafarullah K, Kleinert C, Tromp G, Kuivaniemi H, Kontusaari S, Wu Y, Ganguly A, Prockop DJ. G to A polymorphism in exon 31 of the COL3A1 gene Nucleic Acids Research. 18: 6180. PMID 2235526 DOI: 10.1093/nar/18.20.6180  0.64
1990 Tromp G, Kuivaniemi H, Stolle C, Pope FM, Prockop DJ. Single base mutation in the type III procollagen gene that converts the codon for glycine 883 to aspartate in a proband with mild symptoms of Ehlers-Danlos syndrome IV Annals of the New York Academy of Sciences. 580: 558-559. DOI: 10.1111/j.1749-6632.1990.tb17991.x  0.64
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  0.64
1990 Zhao M, Kontusaari S, Kuivaniemi H, Tromp G, Sabol C, Ala-Kokko L, Klein SA, Ladda RL, Kousseff BG, Prockop DJ. Three single base mutations in type III procollagen gene that prevent correct RNA splicing in variants of Ehlers-Danlos syndrome IV Annals of the New York Academy of Sciences. 580: 554-555. DOI: 10.1111/j.1749-6632.1990.tb17989.x  0.64
1989 Tromp G, Kuivaniemi H, Stolle C, Pope M, Prockop DJ. Single base mutation in the type III procollagen gene that converts the codon for glycine 883 to aspartate in a mild variant of Ehlers-Danlos syndrome IV Journal of Biological Chemistry. 264: 19313-19317. PMID 2808425  0.64
1989 Prockop DJ, Constantinou CD, Dombrowski KE, Hojima Y, Kadler KE, Kuivaniemi H, Tromp G, Vogel BE. Type I procollagen: The gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissue American Journal of Medical Genetics. 34: 60-67. PMID 2683782  0.64
1989 Tromp G, Kuivaniemi H, Shikata H, Prockop DJ. A single base mutation that substitutes serine for glycine 790 of the α1(III) chain of type III procollagen exposes an arginine and causes Ehlers-Danlos syndrome IV Journal of Biological Chemistry. 264: 1349-1352. PMID 2492273  0.64
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