Karl Tryggvason - Concepedia

Author

Karl Tryggvason

Also Known As

Alexander P. Maxwell, Angela Silveira, Enrico Petretto, Gianna M. Toffolo, K Tryggvason, K. TRYGGVASON, K. Tryggvason, KARL TRYGGVASON, Karl TRYGGVASON, Karl Tryggvason

487

Publications

46.9K

Citations

113

H-Index

271

Concepts

All Affiliations

Karolinska Institutet University of Oulu University of Helsinki Biocenter Finland Karolinska University Hospital

About

Karl Tryggvason is an author at Karolinska Institutet specializing in medicine, cell biology, and extracellular matrix.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	76	187	25K
2	Natural Sciences	32	44	6.8K
3	Engineering	9	9	925
4	Health Sciences	6	6	812
5	Public Health	4	4	268

Karl Tryggvason

327

Publications

39.9K

Citations

103

H-Index

Page 1

	Year	Citations
Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome Marjo Kestilä, Ulla Lenkkeri, Minna Männikkö, Molecular Cell GlomerulonephritisDevelopmental BiologyGenetic DisorderCongenital Nephrotic SyndromeGenetics	1998	1.9K
Metastatic potential correlates with enzymatic degradation of basement membrane collagen Lance A. Liotta, Karl Tryggvason, Spiridione Garbisa, Nature Basement Membrane CollagenBiochemistryNatural SciencesTissue PhysiologyMatrix Biology	1980	1.8K
Isolation and characterization of type IV procollagen, laminin, and heparan sulfate proteoglycan from the EHS sarcoma Hynda K. Kleinman, Mary L. McGarvey, Lance A. Liotta, Biochemistry Tissue EngineeringEhs SarcomaImmunologyGlycobiologyPathology	1982	1.2K
Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome David F. Barker, Sirkka Liisa Hostikka, Jing Zhou, Science	1990	872
Impaired endochondral ossification and angiogenesis in mice deficient in membrane-type matrix metalloproteinase I Zhongjun Zhou, Suneel Apte, Raija Soininen, Proceedings of the National Academy of Sciences	2000	786
Nephrin is specifically located at the slit diaphragm of glomerular podocytes Vesa Ruotsalainen, Päivi Ljungberg, Jorma Wartiovaara, Proceedings of the National Academy of Sciences Glomerular DiseaseRenal PathologyCytoskeletonCellular PhysiologyGlomerulonephritis	1999	755
Genomic instability in laminopathy-based premature aging Baohua Liu, Jianming Wang, Kui Ming Chan, Nature Medicine Lifespan ExtensionAgingLongevityGeneticsDegenerative Disease	2005	636
Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy A. Leclerc, Xu Zhang, Haluk Topaloğlu, Nature Genetics Rare DiseasesLaminin α2–Chain GeneDevelopmental BiologyGenetic DisorderMedicine	1995	624
Type IV collagen: structure, gene organization, and role in human diseases. Molecular basis of Goodpasture and Alport syndromes and diffuse leiomyomatosis. Billy G. Hudson, Stephen T. Reeders, Karl Tryggvason Journal of Biological Chemistry FibrosisAlport SyndromesDisease MechanismSurgical PathologyHistopathology	1993	616
X-linked Alport Syndrome Jean Philippe Jaïs, Bertrand Knebelmann, Iannis Giatras, Journal of the American Society of Nephrology	2000	574

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