Anni Evilä

1.6k total citations
20 papers, 644 citations indexed

About

Anni Evilä is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Anni Evilä has authored 20 papers receiving a total of 644 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 13 papers in Cardiology and Cardiovascular Medicine and 8 papers in Genetics. Recurrent topics in Anni Evilä's work include Muscle Physiology and Disorders (17 papers), Cardiomyopathy and Myosin Studies (13 papers) and Neurogenetic and Muscular Disorders Research (8 papers). Anni Evilä is often cited by papers focused on Muscle Physiology and Disorders (17 papers), Cardiomyopathy and Myosin Studies (13 papers) and Neurogenetic and Muscular Disorders Research (8 papers). Anni Evilä collaborates with scholars based in Finland, France and United Kingdom. Anni Evilä's co-authors include Peter Hackman, Bjarne Udd, Bjarne Udd, Anna Vihola, Meharji Arumilli, Johanna Palmio, Patrick F. Chinnery, Per Harald Jonson, Mark Screen and J. Sarparanta and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Anni Evilä

18 papers receiving 632 citations

Peers

Countries citing papers authored by Anni Evilä

Since Specialization

Citations

This map shows the geographic impact of Anni Evilä's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Anni Evilä with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anni Evilä more than expected).

Fields of papers citing papers by Anni Evilä

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anni Evilä. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Anni Evilä. The network helps show where Anni Evilä may publish in the future.

Co-authorship network of co-authors of Anni Evilä

This figure shows the co-authorship network connecting the top 25 collaborators of Anni Evilä. A scholar is included among the top collaborators of Anni Evilä based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Anni Evilä. Anni Evilä is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin gene 2018 ·Neuromuscular Disorders ·K. Kiiski, Vilma‐Lotta Lehtokari, Anna Vihola, Jenni Laitila, Sanna Huovinen, (unknown), Anni Evilä, Anders Paetau, Caroline A. Sewry, Peter Hackman, Katarina Pelin, Carina Wallgren‐Pettersson, Bjarne Udd	29
2	A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy 2017 ·PLoS ONE ·Daniela Rossi, Johanna Palmio, Anni Evilä, Lucia Galli, Virginia Barone, (unknown), (unknown), (unknown), Christopher Berndsen, Nathan T. Wright, Edoardo Malfatti, Guy Brochier, Enrico Pierantozzi, Albena Jordanova, Velina Guergueltcheva, Norma B. Romero, Peter Hackman, B. Eymard, Bjarne Udd, Vincenzo Sorrentino	29
3	A ‘second truncation’ in TTN causes early onset recessive muscular dystrophy 2017 ·Neuromuscular Disorders ·Elizabeth Harris, Ana Töpf, Anna Vihola, Anni Evilä, Rita Barresi, Judith A. Hudson, Peter Hackman, Brian Herron, Daniel G. MacArthur, Hanns Lochmüller, Kate Bushby, Bjarne Udd, Volker Straub	18
4	Targeted Next-Generation Sequencing Reveals Novel TTN Mutations Causing Recessive Distal Titinopathy 2016 ·Molecular Neurobiology ·Anni Evilä, Johanna Palmio, Anna Vihola, Marco Savarese, Giorgio Tasca, Sini Penttilä, Sara Lehtinen, Per Harald Jonson, Jan De Bleecker, Peter P. Rainer, Michaela Auer‐Grumbach, Jean Pouget, Emmanuelle Salort‐Campana, Juan J. Vílchez, Nuria Muelas, Montse Olivé, Peter Hackman, Bjarne Udd	29
5	GNE-Myopathy in a Greek Romani Family with Unusual Calf Phenotype and Protein Aggregation Pathology 2016 ·Journal of Neuromuscular Diseases ·George K. Papadimas, Anni Evilä, Constantinos Papadopoulos, Evangelia Kararizou, Panagiota Manta, Bjarne Udd	5
6	Homozygosity of the Dominant Myotilin c.179C>T (p.Ser60Phe) Mutation Causes a More Severe and Proximal Muscular Dystrophy 2016 ·Journal of Neuromuscular Diseases ·Gabrielle Rudolf, (unknown), Sini Penttilä, Peter Hackman, Anni Evilä, Béatrice Lannes, (unknown), Guillaume Bierry, Christine Tranchant, Bjarne Udd	10
7	Novel mutations in DNAJB6 gene cause a very severe early-onset limb-girdle muscular dystrophy 1D disease 2015 ·Neuromuscular Disorders ·Johanna Palmio, Per Harald Jonson, Anni Evilä, Mari Auranen, Volker Straub, Kate Bushby, Anna Sárközy, Sari Kiuru‐Enari, Satu Sandell, Helena Pihko, Peter Hackman, Bjarne Udd	28
8	Targeted next-generation sequencing reveals novel TTN mutations causing recessive distal titinopathy 2015 ·Neuromuscular Disorders ·Anni Evilä, (unknown), Peter Hackman, Bjarne Udd	5
9	A novel mutation in DNAJB6 causes LGMD1D in two French families 2015 ·Neuromuscular Disorders ·Per Harald Jonson, Anni Evilä, Tanya Stojkovic, Françoise Chapon, H. Luque, Peter Hackman, Bjarne Udd	0
10	Targeted next-generation sequencing assay for detection of mutations in primary myopathies 2015 ·Neuromuscular Disorders ·Anni Evilä, Meharji Arumilli, Bjarne Udd, Peter Hackman	75
11	SQSTM1 splice site mutation in distal myopathy with rimmed vacuoles 2015 ·Neurology ·Robert C. Bucelli, Khalid Arhzaouy, Alan Pestronk, Sara K. Pittman, (unknown), Carolyn M. Sue, Anni Evilä, Peter Hackman, Bjarne Udd, Matthew B. Harms, Conrad C. Weihl	65
12	Isolated semitendinosus involvement in the initial stages of limb-girdle muscular dystrophy 2L 2014 ·Neuromuscular Disorders ·Giorgio Tasca, Anni Evilä, Marika Pane, Mauro Monforte, Alessandra Graziano, Peter Hackman, Eugenio Mercuri, Bjarne Udd	11
13	A.P.4 2014 ·Neuromuscular Disorders ·Anna Vihola, Johanna Palmio, Giorgio Tasca, B. Eymard, Anni Evilä, Stephan Lange, Fengqing Xiang, Lars Edström, Peter Hackman, Mathias Gautel, B. Udd	0
14	G.P.17 2014 ·Neuromuscular Disorders ·Peter Hackman, Anni Evilä, Bjarne Udd	1
15	G.P.20 2014 ·Neuromuscular Disorders ·Anni Evilä, Bjarne Udd, Peter Hackman	1
16	Atypical phenotypes in titinopathies explained by second titin mutations 2014 ·Annals of Neurology ·Anni Evilä, Anna Vihola, J. Sarparanta, Olayinka Raheem, Johanna Palmio, Satu Sandell, B. Eymard, Isabel Illa, Ricard Rojas‐García, Karolina Hankiewicz, Luís Negrão, Tuija Löppönen, Pekka Nokelainen, Mikko Kärppä, Sini Penttilä, Mark Screen, Tiina Suominen, Isabelle Richard, Peter Hackman, Bjarne Udd	63
17	P.3.11 Atypical phenotypes in titinopathies explained by second titin mutations and compound heterozygosity 2013 ·Neuromuscular Disorders ·Anni Evilä, Anna Vihola, J. Sarparanta, (unknown), Satu Sandell, B. Eymard, Isabel Illa, Ricard Rojas‐García, Karolina Hankiewicz, Luís Negrão, Tuija Löppönen, Pekka Nokelainen, Mikko Kärppä, (unknown), Mark Screen, Tiina Suominen, Isabelle Richard, Peter Hackman, B. Udd	2
18	Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5 2012 ·Neurology ·(unknown), Johanna Palmio, Tiina Suominen, (unknown), Anni Evilä, (unknown), Giorgio Tasca, Leigh B. Waddell, Nigel F. Clarke, Alexandru Barboi, Peter Hackman, Bjarne Udd	82
19	Titin mutation segregates with hereditary myopathy with early respiratory failure 2012 ·Brain ·Gerald Pfeffer, Hannah R. Elliott, Helen Griffin, Rita Barresi, James Miller, Julie Marsh, Anni Evilä, Anna Vihola, Peter Hackman, Volker Straub, D J Dick, Rita Horváth, Mauro Santibanez‐Koref, Bjarne Udd, Patrick F. Chinnery	88
20	Welander distal myopathy is caused by a mutation in the RNA‐binding protein TIA1 2012 ·Annals of Neurology ·Peter Hackman, J. Sarparanta, Sara Lehtinen, Anna Vihola, Anni Evilä, Per Harald Jonson, H. Luque, Juha Kere, Mark Screen, Patrick F. Chinnery, Gabrielle Åhlberg, Lars Edström, Bjarne Udd	103

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