Miikka Vikkula (M Vikkula)

Scopus Author ID ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 49

Top Venues

Orphanet journal of rare diseases

American journal of medical genetics. Part A

Journal of medical genetics

Human molecular genetics

Université catholique de Louvain

Université Catholique de Louvain (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Université catholique de Louvain Oct 01 2013

Belgium

Full Professor of Human Genetics :: Human Genetics

Universite Catholique de Louvain Feb 01 1997

Belgium

Prof, Head of lab. :: de Duve Institute, Human Genetics

Education History

Université Catholique de Louvain

Belgium

PHD

University of Helsinki

Finland

PHD

Publications

Nicole Revencu, Astrid Eijkelenboom, Claire Bracquemart, Pia Alhopuro, Judith Armstrong, Eulalia Baselga, Claudia Cesario, Maria Lisa Dentici, Melanie Eyries, Sofia Frisk, Helena Gásdal Karstensen, Nagore Gene-Olaciregui, Sirpa Kivirikko, Cinzia Lavarino, Inger-Lise Mero, Rodolphe Michiels, Elisa Pisaneschi, Bitten Schönewolf-Greulich, Ilse Wieland, Martin Zenker, Miikka Vikkula
Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA. Orphanet journal of rare diseases 19 (1) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, Arie van Haeringen, Gabriela M Repetto, Kathelijn Keymolen, Laurence M Boon, Florence Belva, Guido Giacalone, Nicole Revencu, Yves Sznajer, Katie Riches, Vaughan Keeley, Shehla Mohammed, Kristiana Gordon, Silvia Martin-Almedina, Sara E Dobbins, Pia Ostergaard, Isabelle Quéré, Pascal Brouillard, Miikka Vikkula
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. Human molecular genetics 33 (14) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, Arie van Haeringen, Gabriela M Repetto, Kathelijn Keymolen, Laurence M Boon, Florence Belva, Guido Giacalone, Nicole Revencu, Yves Sznajer, Katie Riches, Vaughan Keeley, Shehla Mohammed, Kristiana Gordon, Silvia Martin-Almedina, Sara E Dobbins, Pia Ostergaard, Isabelle Quéré, Pascal Brouillard, Miikka Vikkula
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. Human molecular genetics 33 (14) (2024)
Emmanuel Seront, Antoine Froidure, Nicole Revencu, Valerie Dekeuleneer, Philippe R M Clapuyt, Dana Dumitriu, Miikka Vikkula, Laurence M Boon
Targeted treatment in complex lymphatic anomaly: a case of synergistic efficacy of trametinib and sirolimus. Orphanet journal of rare diseases 19 (1) (2024)
Emmanuel Seront, Antoine Froidure, Nicole Revencu, Valerie Dekeuleneer, Philippe R M Clapuyt, Dana Dumitriu, Miikka Vikkula, Laurence M Boon
Targeted treatment in complex lymphatic anomaly: a case of synergistic efficacy of trametinib and sirolimus. Orphanet journal of rare diseases 19 (1) (2024)
Annegret Holm, Matthew S Graus, Jill Wylie-Sears, Luke Borgelt, Jerry Wei Heng Tan, Sana Nasim, Long Chung, Ashish Jain, Mingwei Sun, Liang Sun, Pascal Brouillard, Ramrada Lekwuttikarn, Harry Kozakewich, Jacob Yanfei Qi, Joyce C Teng, John B Mulliken, Miikka Vikkula, Mathias Francois, Joyce Bischoff
An endothelial SOX18-mevalonate pathway axis enables repurposing of statins for infantile hemangioma. bioRxiv : the preprint server for biology (2024)
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, Arie van Haeringen, Gabriela M Repetto, Kathelijn Keymolen, Laurence M Boon, Florence Belva, Guido Giacalone, Nicole Revencu, Yves Sznajer, Katie Riches, Vaughan Keeley, Shehla Mohammed, Kristiana Gordon, Silvia Martin-Almedina, Sara E Dobbins, Pia Ostergaard, Isabelle Quéré, Pascal Brouillard, Miikka Vikkula
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. Human molecular genetics 33 (14) (2024)
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, Arie van Haeringen, Gabriela M Repetto, Kathelijn Keymolen, Laurence M Boon, Florence Belva, Guido Giacalone, Nicole Revencu, Yves Sznajer, Katie Riches, Vaughan Keeley, Shehla Mohammed, Kristiana Gordon, Silvia Martin-Almedina, Sara E Dobbins, Pia Ostergaard, Isabelle Quéré, Pascal Brouillard, Miikka Vikkula
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. Human molecular genetics 33 (14) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Nicole Revencu, Astrid Eijkelenboom, Claire Bracquemart, Pia Alhopuro, Judith Armstrong, Eulalia Baselga, Claudia Cesario, Maria Lisa Dentici, Melanie Eyries, Sofia Frisk, Helena Gásdal Karstensen, Nagore Gene-Olaciregui, Sirpa Kivirikko, Cinzia Lavarino, Inger-Lise Mero, Rodolphe Michiels, Elisa Pisaneschi, Bitten Schönewolf-Greulich, Ilse Wieland, Martin Zenker, Miikka Vikkula
Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA. Orphanet journal of rare diseases 19 (1) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A (2024)
Emmanuel Seront, Antoine Froidure, Nicole Revencu, Valerie Dekeuleneer, Philippe R M Clapuyt, Dana Dumitriu, Miikka Vikkula, Laurence M Boon
Targeted treatment in complex lymphatic anomaly: a case of synergistic efficacy of trametinib and sirolimus. Orphanet journal of rare diseases 19 (1) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A (2024)
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, Arie van Haeringen, Gabriela M Repetto, Kathelijn Keymolen, Laurence M Boon, Florence Belva, Guido Giacalone, Nicole Revencu, Yves Sznajer, Katie Riches, Vaughan Keeley, Shehla Mohammed, Kristiana Gordon, Silvia Martin-Almedina, Sara E Dobbins, Pia Ostergaard, Isabelle Quéré, Pascal Brouillard, Miikka Vikkula
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. Human molecular genetics (2024)
Emmanuel Seront, Antoine Froidure, Nicole Revencu, Valerie Dekeuleneer, Philippe R M Clapuyt, Dana Dumitriu, Miikka Vikkula, Laurence M Boon
Targeted treatment in complex lymphatic anomaly: a case of synergistic efficacy of trametinib and sirolimus. Orphanet journal of rare diseases 19 (1) (2024)
Murat Alpaslan, Sandrine Mestré-Godin, Aurélie Lay, Guido Giacalone, Raphaël Helaers, Salma Adham, Hélène Kovacsik, Sophie Guillemard, Erick Mercier, Laurence Boon, Nicole Revencu, Pascal Brouillard, Isabelle Quéré, Miikka Vikkula
Ureteropelvic junction obstruction with primary lymphoedema associated with CELSR1 variants. Journal of medical genetics (2023)
Emmanuel Seront, Jean Marc Biard, An Van Damme, Nicole Revencu, Benoit Lengelé, Sandra Schmitz, Caroline de Toeuf, Philippe R M Clapuyt, Francis Veyckemans, Caroline Prégardien, Miikka Vikkula, Pierre Bernard, Laurence M Boon
A case report of sirolimus use in early fetal management of lymphatic malformation. Nature cardiovascular research 2 (6) (2023)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Anne-Sophie Cloos, Hélène Pollet, Amaury Stommen, Mauriane Maja, Maxime Lingurski, Benedicte Brichard, Catherine Marie Lambert, Patrick Henriet, Christophe E Pierreux, Sebastien Pyr Dit Ruys, Patrick Van Der Smissen, Miikka Vikkula, Laurent Gatto, Manon Martin, Pascal Brouillard, Didier Vertommen, Donatienne Tyteca
Splenectomy improves erythrocyte functionality in spherocytosis based on septin abundance but not maturation defects. Blood advances (2023)
Alexandre Guilhem, Sophie Dupuis-Girod, Olivier Espitia, Sophie Rivière, Julie Seguier, Mallorie Kerjouan, Christian Lavigne, Hélène Maillard, Pascal Magro, Laurent Alric, Dan Lipsker, Antoine Parrot, Vanessa Leguy, Claire Vanlemmens, Laurent Guibaud, Miikka Vikkula, Melanie Eyries, Pierre-Jean Valette, Sophie Giraud
Seven cases of hereditary haemorrhagic telangiectasia-like hepatic vascular abnormalities associated with EPHB4 pathogenic variants. Journal of medical genetics (2023)
Milena Atique Tacla, Matheus de Mello Copelli, Eleonore Pairet, Isabella Lopes Monlleó, Erlane Marques Ribeiro, Elaine Lustosa Mendes, Raphaël Helaers, Társis Antonio Paiva Vieira, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
Molecular investigation in individuals with orofacial clefts and microphthalmia-anophthalmia-coloboma spectrum. European journal of human genetics : EJHG (2023)
Simon Boutry, Raphaël Helaers, Tom Lenaerts, Miikka Vikkula
Excalibur: A new ensemble method based on an optimal combination of aggregation tests for rare-variant association testing for sequencing data. PLoS computational biology 19 (9) (2023)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Simon Boutry, Raphaël Helaers, Tom Lenaerts, Miikka Vikkula
Rare variant association on unrelated individuals in case-control studies using aggregation tests: existing methods and current limitations. Briefings in bioinformatics 24 (6) (2023)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Emmanuel Seront, Jean Marc Biard, An Van Damme, Nicole Revencu, Benoit Lengelé, Sandra Schmitz, Caroline de Toeuf, Philippe R M Clapuyt, Francis Veyckemans, Caroline Prégardien, Miikka Vikkula, Pierre Bernard, Laurence M Boon
A case report of sirolimus use in early fetal management of lymphatic malformation. Nature cardiovascular research 2 (6) (2023)
Alicia B Byrne, Pascal Brouillard, Drew L Sutton, Jan Kazenwadel, Saba Montazaribarforoushi, Genevieve A Secker, Anna Oszmiana, Milena Babic, Kelly L Betterman, Peter J Brautigan, Melissa White, Sandra G Piltz, Paul Q Thomas, Christopher N Hahn, Matthias Rath, Ute Felbor, G Christoph Korenke, Christopher L Smith, Kathleen H Wood, Sarah E Sheppard, Denise M Adams, Ariana Kariminejad, Raphaël Helaers, Laurence M Boon, Nicole Revencu, Lynette Moore, Christopher P Barnett, Eric Haan, Peer Arts, Miikka Vikkula, Hamish S Scott, Natasha L Harvey
Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema. Science translational medicine 14 (634) (2022)
Laurence M Boon, Valérie Dekeuleneer, Julien Coulie, Liliane Marot, Anne-Christine Bataille, Frank Hammer, Philippe R M Clapuyt, Anne Jeanjean, Anne Dompmartin, Miikka Vikkula
Case report study of thalidomide therapy in 18 patients with severe arteriovenous malformations. Nature cardiovascular research 1 (6) (2022)
Anne Dompmartin, Catharina Joanna Maria van der Vleuten, Valerie Dekeuleneer, Thierry Duprez, Nicole Revencu, Julie Désir, D Maroeska W M Te Loo, Uta E Flucke, Astrid Eijkelenboom, Leo Schultze Kool, Miikka Vikkula, Laurence M Boon
GNA11-mutated Sturge-Weber syndrome has distinct neurological and dermatological features. European journal of neurology 29 (10) (2022)
Adrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, Mark K Bakker, Ozan Dikilitas, Soto Romuald Kiando, Lijiang Ma, Benjamin A Satterfield, Sebanti Sengupta, Mengyao Yu, Jean François Deleuze, Delia Dupré, Kristina L Hunker, Sergiy Kyryachenko, Lu Liu, Ines Sayoud-Sadeg, Laurence Amar, Chad M Brummett, Dawn M Coleman, Valentina d'Escamard, Peter W de Leeuw, Natalia Fendrikova-Mahlay, Daniella Kadian-Dodov, Jun Z Li, Aurélien Lorthioir, Marco Pappaccogli, Aleksander Prejbisz, Witold Smigielski, James C Stanley, Matthew Zawistowski, Xiang Zhou, Sebastian Zöllner, null null, null null, null null, Phillippe Amouyel, Marc L De Buyzere, Stephanie Debette, Piotr Dobrowolski, Wojciech Drygas, Heather L Gornik, Jeffrey W Olin, Jerzy Piwonski, Ernst R Rietzschel, Ynte M Ruigrok, Miikka Vikkula, Ewa Warchol Celinska, Andrzej Januszewicz, Iftikhar J Kullo, Michel Azizi, null null, Xavier Jeunemaitre, Alexandre Persu, Jason C Kovacic, Santhi K Ganesh, Nabila Bouatia-Naji
Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nature communications 13 (1) (2022)
Julien Coulie, Laurence M Boon, Miikka Vikkula
Molecular pathways and possible therapies for head and neck vascular anomalies. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology 51 (10) (2022)
Adrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, Mark K Bakker, Ozan Dikilitas, Soto Romuald Kiando, Lijiang Ma, Benjamin A Satterfield, Sebanti Sengupta, Mengyao Yu, Jean François Deleuze, Delia Dupré, Kristina L Hunker, Sergiy Kyryachenko, Lu Liu, Ines Sayoud-Sadeg, Laurence Amar, Chad M Brummett, Dawn M Coleman, Valentina d'Escamard, Peter W de Leeuw, Natalia Fendrikova-Mahlay, Daniella Kadian-Dodov, Jun Z Li, Aurélien Lorthioir, Marco Pappaccogli, Aleksander Prejbisz, Witold Smigielski, James C Stanley, Matthew Zawistowski, Xiang Zhou, Sebastian Zöllner, null null, null null, null null, Phillippe Amouyel, Marc L De Buyzere, Stephanie Debette, Piotr Dobrowolski, Wojciech Drygas, Heather L Gornik, Jeffrey W Olin, Jerzy Piwonski, Ernst R Rietzschel, Ynte M Ruigrok, Miikka Vikkula, Ewa Warchol Celinska, Andrzej Januszewicz, Iftikhar J Kullo, Michel Azizi, Xavier Jeunemaitre, Alexandre Persu, Jason C Kovacic, Santhi K Ganesh, Nabila Bouatia-Naji
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nature communications 12 (1) (2021)
Pascal Brouillard, Matthieu J Schlögel, Nassim Homayun Sepehr, Raphaël Helaers, Angela Queisser, Elodie Fastré, Simon Boutry, Sandra Schmitz, Philippe Clapuyt, Frank Hammer, Anne Dompmartin, Annamaria Weitz-Tuoretmaa, Jussi Laranne, Louise Pasquesoone, Catheline Vilain, Laurence M Boon, Miikka Vikkula
Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations. Orphanet journal of rare diseases 16 (1) (2021)
Veli-Matti Leppänen, Pascal Brouillard, Emilia A Korhonen, Tuomas Sipilä, Sawan Kumar Jha, Nicole Revencu, Veerle Labarque, Elodie Fastré, Matthieu Schlögel, Marie Ravoet, Amihood Singer, Claudia Luzzatto, Donatella Angelone, Giovanni Crichiutti, Angela D'Elia, Jaakko Kuurne, Harri Elamaa, Gou Young Koh, Pipsa Saharinen, Miikka Vikkula, Kari Alitalo
Characterization of ANGPT2 mutations associated with primary lymphedema. Science translational medicine 12 (560) (2021)
Pascal Brouillard, Marlys H Witte, Robert P Erickson, Robert J Damstra, Corinne Becker, Isabelle Quéré, Miikka Vikkula
Primary lymphoedema. Nature reviews. Disease primers 7 (1) (2021)
Richard Coulie, Dmitriy M Niyazov, Michael J Gambello, Elodie Fastré, Pascal Brouillard, Miikka Vikkula
Hypotrichosis-lymphedema-telangiectasia syndrome: Report of ileal atresia associated with a SOX18 de novo pathogenic variant and review of the phenotypic spectrum. American journal of medical genetics. Part A 185 (7) (2021)
Latosinska Agnieszka, Rosa Maria Bruno, Marco Pappaccogli, Alessandra Bacca, Christophe Beauloye, Pierre Boutouyrie, Hakim Khettab, Jan A Staessen, Stefano Taddei, Laurent Toubiana, Miikka Vikkula, Harald Mischak, Alexandre Persu
Increased Collagen Turnover Is a Feature of Fibromuscular Dysplasia and Associated With Hypertrophic Radial Remodeling: A Pilot, Urine Proteomic Study. Hypertension (Dallas, Tex. : 1979) 79 (1) (2021)
Marie F Smeland, Pascal Brouillard, Trine Prescott, Laurence M Boon, Bodil Hvingel, Cecilie V Nordbakken, Mona Nystad, Øystein L Holla, Miikka Vikkula
Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis. Journal of medical genetics (2021)
An Van Damme, Emmanuel Seront, Valerie Dekeuleneer, Laurence M Boon, Miikka Vikkula
New and Emerging Targeted Therapies for Vascular Malformations. American journal of clinical dermatology 21 (5) (2021)
Ines Martinez-Corral, Yan Zhang, Milena Petkova, Henrik Ortsäter, Sofie Sjöberg, Sandra D Castillo, Pascal Brouillard, Louis Libbrecht, Dieter Saur, Mariona Graupera, Kari Alitalo, Laurence Boon, Miikka Vikkula, Taija Mäkinen
Blockade of VEGF-C signaling inhibits lymphatic malformations driven by oncogenic PIK3CA mutation. Nature communications 11 (1) (2020)
Hélène Pollet, Anne-Sophie Cloos, Amaury Stommen, Juliette Vanderroost, Louise Conrard, Adrien Paquot, Marine Ghodsi, Mélanie Carquin, Catherine Léonard, Manuel Guthmann, Maxime Lingurski, Christiane Vermylen, Theodore Killian, Laurent Gatto, Mark Rider, Sebastien Pyr Dit Ruys, Didier Vertommen, Miikka Vikkula, Pascal Brouillard, Patrick Van Der Smissen, Giulio G Muccioli, Donatienne Tyteca
Aberrant Membrane Composition and Biophysical Properties Impair Erythrocyte Morphology and Functionality in Elliptocytosis. Biomolecules 10 (8) (2020)
Nicole Revencu, Elodie Fastre, Marie Ravoet, Raphaël Helaers, Pascal Brouillard, Annouk Bisdorff-Bresson, Clara W T Chung, Marion Gerard, Veronika Dvorakova, Alan D Irvine, Laurence M Boon, Miikka Vikkula
RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation. Journal of medical genetics 57 (1) (2019)
Mirta Basha, Bénédicte Demeer, Nicole Revencu, Raphael Helaers, Stephanie Theys, Sami Bou Saba, Odile Boute, Bernard Devauchelle, Geneviève Francois, Bénédicte Bayet, Miikka Vikkula
Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes. Journal of medical genetics 55 (7) (2018)
E Fastré, L-E Lanteigne, R Helaers, G Giacalone, N Revencu, D Dionyssiou, E Demiri, P Brouillard, Miikka Vikkula
Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema. Clinical genetics 94 (1) (2018)
Silvia Di Monaco, Adrien Georges, Jean-Philippe Lengelé, Miikka Vikkula, Alexandre Persu
Genomics of Fibromuscular Dysplasia. International journal of molecular sciences 19 (5) (2018)
Aniel Jessica Leticia Brambila-Tapia, José Elías García-Ortiz, Pascal Brouillard, Ha-Long Nguyen, Miikka Vikkula, Blanca Esthela Rios-Gonzalez, Roberto de Jesús Sandoval-Muñiz, Ana Karen Sandoval-Talamantes, Lucina Bobadilla-Morales, Jorge Román Corona-Rivera, Lisette Arnaud-Lopez
GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome. Hematology (Amsterdam, Netherlands) 22 (8) (2017)

Miikka Vikkula.css-eqlu8i{font-size:small;padding-left:4px;} (M Vikkula)

Publication Activity (10 Years)

Top Topics

Top Venues

Miikka Vikkula (M Vikkula)