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Author
Miikka Vikkula
also known as M Vikkula, M. Vikkula, Miikka S. Vikkula
Université Claude Bernard Lyon 1 · Boston Children's Hospital · Cliniques Universitaires Saint-Luc · European Union
About this author
Works
952
Cited by
27,043
h-index
83
i10
217
ORCID ↗
Top papers
LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development
Yaoqin Gong, Roger B. Slee, Naomi Fukai, et al.
·
2001
·
Cell
↗ 2,236
OA
Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies
Michel Wassef, Francine Blei, Denise M. Adams, et al.
·
2015
·
PEDIATRICS
↗ 1,374
Chromosome instability is common in human cleavage-stage embryos
Evelyne Vanneste, Thierry Voet, Cédric Le Caignec, et al.
·
2009
·
Nature Medicine
↗ 894
Vascular Dysmorphogenesis Caused by an Activating Mutation in the Receptor Tyrosine Kinase TIE2
Miikka Vikkula, Laurence M. Boon, Kermit L. Carraway, et al.
·
1996
·
Cell
↗ 808
OA
Capillary Malformation–Arteriovenous Malformation, a New Clinical and Genetic Disorder Caused by RASA1 Mutations
Iiro Eerola, Laurence M. Boon, John B. Mulliken, et al.
·
2003
·
The American Journal of Human Genetics
↗ 749
OA
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
Twinkal C. Pansuriya, Ronald van Eijk, Pio D’Adamo, et al.
·
2011
·
Nature Genetics
↗ 554
OA
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis
Bettina Lorenz‐Depiereux, Murat Bastepe, Anna Benet‐Pagès, et al.
·
2006
·
Nature Genetics
↗ 524
OA
Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations
Nisha Limaye, Vinciane Wouters, Mélanie Uebelhoer, et al.
·
2008
·
Nature Genetics
↗ 491
OA
Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase
Alexandre Irrthum, Marika J. Karkkainen, Koenraad Devriendt, et al.
·
2000
·
The American Journal of Human Genetics
↗ 434
OA
Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia
Alexandre Irrthum, Koenraad Devriendt, David Chitayat, et al.
·
2003
·
The American Journal of Human Genetics
↗ 428
OA
Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused byRASA1 mutations
Nicole Revençu, Laurence M. Boon, John B. Mulliken, et al.
·
2008
·
Human Mutation
↗ 427
OA
Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus
Miikka Vikkula, Edwin C.M Madman, Vincent Chi Hang Lui, et al.
·
1995
·
Cell
↗ 409
OA