All papers authored by Booth Kt
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2021
Barbara Vona 
,
Neda Mazaheri ,
Sheng-Jia Lin ,
Lucy A. Dunbar ,
Reza Maroofian,
Hela Azaiez ,
Kevin T. Booth ,
Sandrine Vitry ,
Aboulfazl Rad ,
Franz Rüschendorf ,
Pratishtha Varshney ,
Ben Fowler,
Christian Beetz ,
Kumar N. Alagramam,
David Murphy
and 11 other authors
,
Neda Mazaheri ,
Sheng-Jia Lin ,
Lucy A. Dunbar ,
Reza Maroofian,
Hela Azaiez ,
Kevin T. Booth ,
Sandrine Vitry ,
Aboulfazl Rad ,
Franz Rüschendorf ,
Pratishtha Varshney ,
Ben Fowler,
Christian Beetz ,
Kumar N. Alagramam,
David Murphy
and 11 other authors
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
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2019
Matias Morin,
Andrea M. Oza,
Rebecca K. Siegert,
Ahmad N. Abou Tayoun,
Tatsuo Matsunaga,
Jun Shen,
Wenying Zhang,
Lisa A. Schimmenti,
Mustafa Tekin,
Heidi L. Rehm,
Ignacio del Castillo,
Lim Jiin Ying,
Suzanne Leal,
Morag Lewis,
Xue Zhong Liu
and 58 other authors
ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs
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2018
Andrea M. Oza,
Rebecca K. Siegert,
Jun Shen,
Lisa A. Schimmenti,
Jaclyn B. Murry,
Kiyomitsu Nara,
Heidi L. Rehm,
Marina T. DiStefano,
Sarah E. Hemphill,
Brandon J. Cushman,
Andrew R. Grant,
Alex Chapin,
Nicole J. Boczek,
Linda Hasadsri,
Margaret Kenna
and 8 other authors
Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss.
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