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3,541 authors found
quering by "Smooth Muscle Alpha-Actin Mutations"
.
Showing
the first 25
sort by ONE Index.
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913
One Index
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Wilkie, Andrew PhD 0000-0002-2972-5481 |
432 docs (1982 - 2024)
Craniosynostosis , Haploinsufficiency , Apert syndrome , Medical genetics , Craniosynostoses |
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912
One Index
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Milewicz, Dianna PhD 0000-0002-7806-0068 |
476 docs (1977 - 2024)
Aortic Dissection , Type B Aortic Dissection , Aortic Aneurysms , Thoracic Aortic Aneurysms , Thoracic aortic aneurysm |
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907
One Index
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Durbeej Hjalt, Madeleine PhD 0000-0002-5491-2457 |
227 docs (1981 - 2024)
Dystroglycan , Congenital muscular dystrophy , Skeletal Muscle Atrophy , Spindle pole body , Centriole |
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906
One Index
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Darwin J. Prockop PhD |
690 docs (1958 - 2019)
Procollagen peptidase , Hydroxyproline , Stromal Cells , Collagen , Mesenchymal Stem Cells |
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896
One Index
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Spits, Hergen PhD 0000-0003-3269-8338 |
452 docs (1975 - 2024)
Innate lymphoid cell , Memory T Cells , Innate Lymphoid Cells , NK Cell Development , NK Cell Recognition |
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893
One Index
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Byers, Peter H. PhD 0000-0001-7786-7030 |
404 docs (1972 - 2024)
Osteogenesis Imperfecta , Ehlers–Danlos syndrome , Procollagen peptidase , Ehlers-Danlos Syndrome , Type I collagen |
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890
One Index
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Hedges, Larry PhD 0000-0002-7531-0631 |
671 docs (1975 - 2024)
Meta-Analysis , Gaucher Disease , Neurofibromatosis , Achondroplasia , Research Methodology |
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881
One Index
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Dobyns, William PhD 0000-0002-7681-2844 |
600 docs (1979 - 2024)
Polymicrogyria , Microcephaly , Cerebellar Malformations , Pachygyria , Brain Development |
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877
One Index
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Mundlos, Stefan PhD 0000-0002-9788-3166 |
662 docs (1986 - 2024)
Brachydactyly , Limb Malformations , Polydactyly , Cutis laxa , Syndactyly |
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875
One Index
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Jeffrey Robert Gulcher PhD 0009-0000-4433-2072 |
308 docs (1979 - 2024)
Genome-wide association study , Bone remodeling , Genetic association , Genetic linkage , SNP |
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874
One Index
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Loeys, Bart PhD 0000-0003-3703-9518 |
420 docs (1998 - 2024)
Marfan Syndrome , Aortic Dissection , Aortic Aneurysms , Thoracic aortic aneurysm , Fibrillin |
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872
One Index
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Morava, Eva PhD 0000-0001-7441-700X |
646 docs (1964 - 2024)
Inborn Errors of Metabolism , Glycosylation , Cutis laxa , Protein Glycosylation , Mitochondrial disease |
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870
One Index
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Lu, Hong PhD 0000-0002-0577-2558 |
281 docs (1996 - 2024)
Aortic Aneurysms , Aortic Dissection , Angiotensin , Thoracic Aortic Aneurysms , Type B Aortic Dissection |
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868
One Index
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Ramirez, Francesco PhD 0000-0002-2668-8785 |
347 docs (1972 - 2024)
Fibrillin , Fibrillin-1 , Marfan Syndrome , Microfibril , Alpha (finance) |
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868
One Index
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Dietz, Harry PhD 0000-0002-6856-0165 |
381 docs (1952 - 2024)
Marfan Syndrome , Fibrillin , Aortic Dissection , Aortic Root Replacement , Aortic Aneurysms |
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868
One Index
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Ikegawa, Shiro PhD 0000-0003-0316-2147 |
500 docs (1990 - 2024)
Genome-wide association study , Genetic association , Adolescent Idiopathic Scoliosis , SNP , Osteoarthritis |
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865
One Index
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Daugherty, Alan PhD 0000-0003-2093-3775 |
544 docs (1981 - 2024)
Aortic Aneurysms , Aortic Dissection , Apolipoprotein E , Thoracic Aortic Aneurysms , Angiotensin |
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865
One Index
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LIN, Angela PhD 0000-0002-1145-4572 |
302 docs (1982 - 2024)
Costello syndrome , Turner Syndrome , Congenital Heart Defects , Adult Congenital Heart Disease , Congenital Heart Disease |
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862
One Index
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Keene, Douglas PhD 0000-0003-2986-370X |
329 docs (1982 - 2024)
Fibrillin , Epidermolysis Bullosa , Cell Adhesion , Fibrillin-1 , Anchoring fibrils |
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859
One Index
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Krakow, Deborah PhD 0000-0001-9906-4968 |
291 docs (1983 - 2024)
Osteogenesis Imperfecta , FLNA , Fetal DNA Analysis , Polydactyly , Smooth Muscle Alpha-Actin Mutations |
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859
One Index
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Fikree, Asma PhD |
91 docs (2008 - 2024)
Joint hypermobility , Hypermobility (travel) , Ehlers–Danlos syndrome , Ehlers-Danlos Syndrome , Esophageal Motility Disorders |
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859
One Index
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De Backer, Julie PhD 0000-0001-8878-1507 |
651 docs (1924 - 2024)
Marfan Syndrome , Aortic Dissection , Aortic Aneurysms , Adult Congenital Heart Disease , Fibrillin |
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858
One Index
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Al-Gazali, Lihadh PhD 0000-0003-2029-2218 |
260 docs (1988 - 2023)
Microcephaly , Joubert syndrome , Exome , Haploinsufficiency , Loss function |
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856
One Index
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Bacino, Carlos PhD 0000-0002-4342-5012 |
303 docs (1988 - 2024)
Haploinsufficiency , Comparative genomic hybridization , Achondroplasia , Microcephaly , Neurodevelopmental disorder |
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855
One Index
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De Paepe, Anne PhD 0000-0002-4134-5940 |
327 docs (1987 - 2023)
Ehlers–Danlos syndrome , Ehlers-Danlos Syndrome , Joint hypermobility , Osteogenesis Imperfecta , Marfan Syndrome |
