D-Index & Metrics Best Publications

Miikka Vikkula

Cliniques Universitaires Saint-Luc
Belgium

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name Citations Publications World Ranking National Ranking

Medicine D-index 76 Citations 22,607 316 World Ranking 13888 National Ranking 172

Genetics D-index 71 Citations 21,286 274 World Ranking 1482 National Ranking 22

Overview

What is he best known for?

The fields of study Miikka Vikkula is best known for:

Gene
Enzyme
Cancer

In the subject of Surgery, Miikka Vikkula integrates adjacent scientific disciplines such as Venous malformation and Vascular malformation. Venous malformation is frequently linked to Radiology in his study. Radiology and Arteriovenous malformation are commonly linked in his work. Vascular malformation and Surgery are commonly linked in his work. He incorporates Genetics and Cancer research in his research. He undertakes multidisciplinary studies into Cancer research and Genetics in his work. Miikka Vikkula performs multidisciplinary studies into Gene and Exon in his work. In his works, he conducts interdisciplinary research on Exon and Gene. Miikka Vikkula integrates many fields in his works, including Mutation and Phenotype.

His most cited work include:

LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development (2006 citations)
Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies (888 citations)
Vascular Dysmorphogenesis Caused by an Activating Mutation in the Receptor Tyrosine Kinase TIE2 (716 citations)

What are the main themes of his work throughout his whole career to date

Miikka Vikkula performs integrative study on Genetics and Cancer research in his works. Borrowing concepts from Genetics, he weaves in ideas under Cancer research. Miikka Vikkula merges many fields, such as Gene and Somatic cell, in his writings. Miikka Vikkula performs integrative study on Somatic cell and Gene. Miikka Vikkula undertakes interdisciplinary study in the fields of Pathology and Radiology through his research. He conducted interdisciplinary study in his works that combined Radiology and Pathology. His work often combines Mutation and Germline mutation studies. His Internal medicine study frequently draws connections to other fields, such as Cancer. Many of his studies involve connections with topics such as Internal medicine and Cancer.

Miikka Vikkula most often published in these fields:

Genetics (80.35%)
Gene (69.94%)
Pathology (42.20%)

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development

Y. Q. Gong;R. B. Slee;N. Fukai;G. Rawadi.
Cell (2001)

2505 Citations

Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies

Michel Wassef;Francine Blei;Denise Adams;Ahmad Alomari.
Pediatrics (2015)

1003 Citations

Vascular Dysmorphogenesis Caused by an Activating Mutation in the Receptor Tyrosine Kinase TIE2

Miikka Vikkula;Laurence M Boon;Kermit L.Carraway;Jennifer T Calvert.
Cell (1996)

896 Citations

CHROMOSOME INSTABILITY IS COMMON IN HUMAN CLEAVAGE-STAGE EMBRYOS

Evelyne Vanneste;Thierry Voet;Cédric Le Caignec;Cédric Le Caignec;Michèle Ampe.
Nature Medicine (2009)

848 Citations

Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations.

Iiro Eerola;Laurence M. Boon;John B. Mulliken;Patricia E. Burrows.
American Journal of Human Genetics (2003)

713 Citations

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;Mustapha Amyere.
Nature Genetics (2006)

521 Citations

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;Maayke A. J. H. van Ruler.
Nature Genetics (2011)

498 Citations

Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase

Alexandre Irrthum;Marika J. Karkkainen;Koen Devriendt;Kari Alitalo.
American Journal of Human Genetics (2000)

479 Citations

Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.

Alexandre Irrthum;Koenraad Devriendt;David Chitayat;Gert Matthijs.
American Journal of Human Genetics (2003)

457 Citations

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

Miikka Vikkula;Edwin C.M Madman;Vincent C.H Lui;Natalia I Zhidkova.
Cell (1995)

415 Citations

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Frequent Co-Authors

External Links

Personal Website for Miikka Vikkula