Julie Hathaway

Years Active: 2019-2021
Publications (10 Years): 3

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

Publications

Juha W Koskenvuo, Inka Saarinen, Saija Ahonen, Johanna Tommiska, Sini Weckström, Eija H Seppälä, Sari Tuupanen, Tiia Kangas-Kontio, Jennifer Schleit, Krista Heliö, Julie Hathaway, Anders Gummesson, Pia Dahlberg, Tiina H Ojala, Ville Vepsäläinen, Ville Kytölä, Mikko Muona, Johanna Sistonen, Pertteli Salmenperä, Massimiliano Gentile, Jussi Paananen, Samuel Myllykangas, Tero-Pekka Alastalo, Tiina Heliö
Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy. PloS one 16 (2) (2021)
Julie Hathaway, Krista Heliö, Inka Saarinen, Jonna Tallila, Eija H Seppälä, Sari Tuupanen, Hannu Turpeinen, Tiia Kangas-Kontio, Jennifer Schleit, Johanna Tommiska, Ville Kytölä, Miko Valori, Mikko Muona, Johanna Sistonen, Massimiliano Gentile, Pertteli Salmenperä, Samuel Myllykangas, Jussi Paananen, Tero-Pekka Alastalo, Tiina Heliö, Juha Koskenvuo
Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients. BMC cardiovascular disorders 21 (1) (2021)
Mireille Cloutier, Julie Hathaway, Rachel Vanneste, Priscila Delgado Hodges, Guillaume Sillon
Lexigene®: An online medical genetics translation tool to facilitate communication. Journal of genetic counseling 28 (3) (2019)

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