All papers authored by Chiara Klöckner
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2022
Chiara Klöckner 
,
J. Pedro Fernández-Murray ,
Mahtab Tavasoli ,
Heinrich Sticht ,
Gisela Stoltenburg-Didinger ,
Leila Motlagh Scholle ,
Somayeh Bakhtiari,
Michael C. Kruer ,
Hossein Darvish,
Saghar Ghasemi Firouzabadi ,
Alex Pagnozzi,
Anju Shukla ,
Katta Mohan Girisha ,
Dhanya Lakshmi Narayanan ,
Parneet Kaur
and 14 other authors
,
J. Pedro Fernández-Murray ,
Mahtab Tavasoli ,
Heinrich Sticht ,
Gisela Stoltenburg-Didinger ,
Leila Motlagh Scholle ,
Somayeh Bakhtiari,
Michael C. Kruer ,
Hossein Darvish,
Saghar Ghasemi Firouzabadi ,
Alex Pagnozzi,
Anju Shukla ,
Katta Mohan Girisha ,
Dhanya Lakshmi Narayanan ,
Parneet Kaur
and 14 other authors
Bi-allelic variants inCHKAcause a neurodevelopmental disorder with epilepsy and microcephaly
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2021
Chiara Klöckner ,
J. Pedro Fernandez Murray,
Mahtab Tavasoli,
Heinrich Sticht,
Gisela Stoltenburg-Didinger,
Leila Motlagh Scholle ,
Somayeh Bakhtiari,
Michael C. Kruer ,
Hossein Darvish,
Saghar Ghasemi Firouzabadi ,
Alex Pagnozzi,
Anju Shukla,
Katta Mohan Girisha,
Dhanya Lakshmi Narayanan,
Parneet Kaur
and 14 other authors
,
J. Pedro Fernandez Murray,
Mahtab Tavasoli,
Heinrich Sticht,
Gisela Stoltenburg-Didinger,
Leila Motlagh Scholle ,
Somayeh Bakhtiari,
Michael C. Kruer ,
Hossein Darvish,
Saghar Ghasemi Firouzabadi ,
Alex Pagnozzi,
Anju Shukla,
Katta Mohan Girisha,
Dhanya Lakshmi Narayanan,
Parneet Kaur
and 14 other authors
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly
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Chiara Klöckner ,
Heinrich Sticht,
Pia Zacher,
Bernt Popp,
Holly E. Babcock,
Dewi P. Bakker,
Katy Barwick,
Michaela V. Bonfert,
Carsten G. Bönnemann,
Eva H. Brilstra,
Wendy K. Chung,
Angus J. Clarke,
Patrick Devine,
Sandra Donkervoort,
Jamie L. Fraser
and 43 other authors
,
Heinrich Sticht,
Pia Zacher,
Bernt Popp,
Holly E. Babcock,
Dewi P. Bakker,
Katy Barwick,
Michaela V. Bonfert,
Carsten G. Bönnemann,
Eva H. Brilstra,
Wendy K. Chung,
Angus J. Clarke,
Patrick Devine,
Sandra Donkervoort,
Jamie L. Fraser
and 43 other authors
De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy
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