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Publications for Ekaterina Kuchinskaya


Co-author map based on Web of Sciences articles 2007-

Publications mentioned in social media 22 times*

Journal Articles

Jin J. Zhao, Jonatan Halvardson, Cecilia S. Zander, Ammar Zaghlool, Patrik Georgii-Hemming, Else Mansson, Göran Brandberg, Helena E. Savmarker, Carina Frykholm, Ekaterina Kuchinskaya, Ann-Charlotte Thuresson and Lars Feuk
  Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability
  American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2018, 177(1), 10-20.

Eva Fernlund, Anna Wålinder Österberg, Ekaterina Kuchinskaya, Mikael Gustafsson, Kjell Jansson and Cecilia Gunnarsson
  Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death
  Pediatric Cardiology, 2017, 38(6), 1262-1268.
   Fulltext  PDF  

Ekaterina Kuchinskaya, Giedre Grigelioniene, Anna Hammarsjo, Hye-Ran Lee, Lotta Högberg, Gintautas Grigelionis, Ok-Hwa Kim, Gen Nishimura and Tae-Joon Cho
  Extending the phenotype of BMPER-related skeletal dysplasias to ischiospinal dysostosis
  Orphanet Journal of Rare Diseases, 2016, 11(1), .
   Fulltext  PDF  
 Web of Science® Times Cited: 1

Maria Concepcion Gil-Rodriguez, Matthew A. Deardorff, Morad Ansari, Christopher A. Tan, Ilaria Parenti, Carolina Baquero-Montoya, Lilian B. Ousager, Beatriz Puisac, Maria Hernandez-Marcos, Maria Esperanza Teresa-Rodrigo, Inigo Marcos-Alcalde, Jan-Jaap Wesselink, Silvia Lusa-Bernal, Emilia K. Bijlsma, Diana Braunholz, Ines Bueno-Martinez, Dinah Clark, Nicola S. Cooper, Cynthia J. Curry, Richard Fisher, Alan Fryer, Jaya Ganesh, Cristina Gervasini, Gabriele Gillessen-Kaesbach, Yiran Guo, Hakon Hakonarson, Robert J. Hopkin, Maninder Kaur, Brendan J. Keating, Maria Kibaek, Esther Kinning, Tjitske Kleefstra, Antonie D. Kline, Ekaterina Kuchinskaya, Lidia Larizza, Yun R. Li, Xuanzhu Liu, Milena Mariani, Jonathan D. Picker, Angeles Pie, Jelena Pozojevic, Ethel Queralt, Julie Richer, Elizabeth Roeder, Anubha Sinha, Richard H. Scott, Joyce So, Katherine A. Wusik, Louise Wilson, Jianguo Zhang, Paulino Gomez-Puertas, Cesar H. Casale, Lena Stroem, Angelo Selicorni, Feliciano J. Ramos, Laird G. Jackson, Ian D. Krantz, Soma Das, Raoul C. M. Hennekam, Frank J. Kaiser, David R. FitzPatrick and Juan Pie
  De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia de Lange Syndrome-Overlapping Phenotypes
  Human Mutation, 2015, 36(4), 454-462.
 Web of Science® Times Cited: 19

* Social media data based on publications from 2011 to present and with a DOI; data delivered by Altmetric.com.

 



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Last updated: 2017-02-21