Laura Schultz-Rogers
4PUBLICATIONS
31CO-AUTHORS
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Publications (4)
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|Sep 12, 2020
Haploinsufficiency as a disease mechanism in GNB1-associated neurodevelopmental disorder.Laura Schultz-Rogers, Ikuo Masuho, Filippo Pinto E Vairo
|Feb 01, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.Holger Hengel, Célia Bosso-Lefèvre, George Grady
|Oct 13, 2019
Novel biallelic variants in <i>MSTO1</i> associated with mitochondrial myopathy.Laura Schultz-Rogers, Alejandro Ferrer, Nikita R Dsouza
|Jul 14, 2019
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.Vincenzo Salpietro, Christine L Dixon, Hui Guo
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Frequent Collaborators
1 joint publications
Holger Hengel
1 joint publications
Élise Lebigot
1 joint publications
Renske Oegema
1 joint publications
Tyler Mark Pierson
1 joint publications
Marisa V Andrews
1 joint publications
Tahsin Stefan Barakat
1 joint publications
Tal Gilboa
1 joint publications
Ingo Helbig
1 joint publications
Suleyman Gulsuner
1 joint publications
Sabina Barresi
