Eeva‐Marja Sankila

1.5k total citations
38 papers, 1.1k citations indexed

About

Eeva‐Marja Sankila is a scholar working on Molecular Biology, Ophthalmology and Sensory Systems. According to data from OpenAlex, Eeva‐Marja Sankila has authored 38 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 13 papers in Ophthalmology and 11 papers in Sensory Systems. Recurrent topics in Eeva‐Marja Sankila's work include Retinal Development and Disorders (14 papers), Hearing, Cochlea, Tinnitus, Genetics (11 papers) and Retinal Diseases and Treatments (9 papers). Eeva‐Marja Sankila is often cited by papers focused on Retinal Development and Disorders (14 papers), Hearing, Cochlea, Tinnitus, Genetics (11 papers) and Retinal Diseases and Treatments (9 papers). Eeva‐Marja Sankila collaborates with scholars based in Finland, United States and Netherlands. Eeva‐Marja Sankila's co-authors include Albert de la Chapelle, Leenamaija Pakarinen, Frans P.M. Cremers, Anna‐Elina Lehesjoki, Tarja Joensuu, H Kääriäinen, Kristiina Aittomäki, José A. J. M. van den Hurk, Riikka H. Hämäläinen and S. Karjalainen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Ophthalmology.

In The Last Decade

Eeva‐Marja Sankila

35 papers receiving 1.1k citations

Peers

Countries citing papers authored by Eeva‐Marja Sankila

Since Specialization

Citations

This map shows the geographic impact of Eeva‐Marja Sankila'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 Eeva‐Marja Sankila with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eeva‐Marja Sankila more than expected).

Fields of papers citing papers by Eeva‐Marja Sankila

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eeva‐Marja Sankila. 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 Eeva‐Marja Sankila. The network helps show where Eeva‐Marja Sankila may publish in the future.

Co-authorship network of co-authors of Eeva‐Marja Sankila

This figure shows the co-authorship network connecting the top 25 collaborators of Eeva‐Marja Sankila. A scholar is included among the top collaborators of Eeva‐Marja Sankila 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 Eeva‐Marja Sankila. Eeva‐Marja Sankila 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	Characterisation of a LINE-1 Insertion in the RP1 Gene by Targeted Adaptive Nanopore Sequencing in a Family with Retinitis Pigmentosa 2024 ·Human Mutation ·Michael Backlund, Pauliina Repo, (unknown), Kati Donner, Eeva‐Marja Sankila, (unknown), (unknown), Kirmo Wartiovaara, Tero Kivelä, Joni A. Turunen	0
2	A Prospective, Observational, Non-interventional Clinical Study of Participants With Choroideremia: The NIGHT Study 2024 ·American Journal of Ophthalmology ·Robert E. MacLaren, Byron L. Lam, Manuel Fischer, Frank G. Holz, Mark E. Pennesi, David G. Birch, Eeva‐Marja Sankila, Isabelle Meunier, Kimberly E. Stepien, Juliana Maria Ferraz Sallum, (unknown), (unknown), (unknown), James A. Gow	4
3	A retrospective longitudinal study of 52 Finnish patients with X‐linked retinoschisis 2024 ·Acta Ophthalmologica ·Mika Järvinen, Rigmor C. Baraas, Anna Majander, Michael Backlund, (unknown), (unknown), Päivi Lindahl, (unknown), Eeva‐Marja Sankila, Tero Kivelä, Joni A. Turunen	0
4	Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG 2022 ·Acta Ophthalmologica ·Anna Majander, Eeva‐Marja Sankila, Aura Falck, (unknown), Sanna Seitsonen, (unknown), (unknown), Kristiina Avela, Joni A. Turunen	3
5	The cone-dominant retina and the inner ear of zebrafish express the ortholog of CLRN1, the causative gene of human Usher syndrome type 3A 2013 ·Gene Expression Patterns ·Jennifer B. Phillips, (unknown), Jeremy Wegner, Aurélie Clément, Eeva‐Marja Sankila, Monte Westerfield	13
6	Penetrance and Phenotype of the Thr377MetMyocilinMutation in a Large Finnish Family with Juvenile- and Adult-Onset Primary Open-Angle Glaucoma 2005 ·Ophthalmic Genetics ·Päivi Puska, Susanna Lemmelä, Paula Kristo, Eeva‐Marja Sankila, Irma Järvelä	21
7	Serial Audiometry and Speech Recognition Findings in Finnish Usher Syndrome Type III Patients 2005 ·Audiology and Neurotology ·(unknown), Leenamaija Kleemola, P.L.M. Huygen, Tarja Joensuu, Eeva‐Marja Sankila, Ronald J. E. Pennings, Cor W. R. J. Cremers	26
8	Dominant optic atrophy: correlation between clinical and molecular genetic studies 2005 ·Acta Ophthalmologica Scandinavica ·(unknown), Kirsi Huoponen, Maija Mäntyjärvi, (unknown), (unknown), Eeva‐Marja Sankila, Marja‐Liisa Savontaus, Mirja Somer, Eeva Nikoskelainen	46
9	The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study. 2003 ·PubMed ·Eva Forsman, Susanna Lemmelä, Teppo Varilo, Paula Kristo, Henrik Forsius, Eeva‐Marja Sankila, Irma Järvelä	32
10	Mutations in a Novel Gene with Transmembrane Domains Underlie Usher Syndrome Type 3 2001 ·The American Journal of Human Genetics ·Tarja Joensuu, Riikka H. Hämäläinen, Bo Yuan, Cheryl K.H. Johnson, Saara Tegelberg, Paolo Gasparini, Leopoldo Zelante, Ulla Pirvola, Leenamaija Pakarinen, Anna‐Elina Lehesjoki, Albert de la Chapelle, Eeva‐Marja Sankila	161
11	A Sequence-Ready Map of the Usher Syndrome Type III Critical Region on Chromosome 3q 2000 ·Genomics ·Tarja Joensuu, Riikka H. Hämäläinen, Anna‐Elina Lehesjoki, Albert de la Chapelle, Eeva‐Marja Sankila	17
12	In vivo confocal microscopy of a family with schnyder crystalline corneal dystrophy11The authors have no proprietary interest in the equipment used in this study. 1999 ·Ophthalmology ·Minna Vesaluoma, Tuuli Linna, Eeva‐Marja Sankila, Jayne S. Weiss, Timo Tervo	46
13	Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3 1995 ·Human Molecular Genetics ·Maria Bitner‐Glindzicz, Peter D. Turnpenny, Pia Höglund, Helena Kääriäinen, Eeva‐Marja Sankila, Silvère M. van der Maarel, Yvette J.M. de Kok, Hans‐Hilger Ropers, Frans P.M. Cremers, (unknown), S Malcolm	58
14	Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q 1995 ·Human Molecular Genetics ·Eeva‐Marja Sankila, Leenamaija Pakarinen, H Kääriäinen, Kristiina Aittomäki, S. Karjalainen, P. Sistonen, Albert de la Chapelle	119
15	The existence of Usher syndrome type III proven by assignment of its locus to chromosome 3q by linkage 1994 ·The American Journal of Human Genetics ·Eeva‐Marja Sankila, (unknown), (unknown)	5
16	Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients 1994 ·Human Molecular Genetics ·Hans van Bokhoven, Marianne Schwartz, Sten Andréasson, José A. J. M. van den Hurk, (unknown), Marcelle Jay, Klaus Rüther, Barrie Jay, I. H. Pawlowitzki, Eeva‐Marja Sankila, Alan F. Wright, Hans‐Hilger Ropers, Thomas Rosenberg, Frans P.M. Cremers	60
17	Aberrant splicing of the CHM gene is a significant cause of choroideremia 1992 ·Nature Genetics ·Eeva‐Marja Sankila, (unknown), José A. J. M. van den Hurk, Frans P.M. Cremers, Albert de la Chapelle	70
18	Choroideremia: linkage analysis with physically mapped close DNA-markers 1991 ·Human Genetics ·Eeva‐Marja Sankila, (unknown), Frans P.M. Cremers, Albert de la Chapelle	6
19	DXS26 (HU16) is located in Xq21.1 1990 ·Human Genetics ·Eeva‐Marja Sankila, G.A.P. Bruns, Marianne Schwartz, Eeva Nikoskelainen, E. Niebuhr, Shirley V. Hodgson, Alan F. Wright, Albert de la Chapelle	9
20	Haplotype and multipoint linkage analysis in Finnish choroideremia families 1989 ·Human Genetics ·Eeva‐Marja Sankila, Thomas Lehner, Aldur W. Eriksson, Henrik Forsius, (unknown), David C. Page, Jürg Ott, Albert de la Chapelle	12

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