Publications by authors named "Ana Claasen"

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Spatial and temporal transmission dynamics of respiratory syncytial virus in New Zealand before and after the COVID-19 pandemic.
Lauren Jelley, Jordan Douglas, Meaghan O'Neill, Klarysse Berquist, Ana Claasen

Nat Commun· November 2024

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Spatial and temporal transmission dynamics of respiratory syncytial virus in New Zealand before and after the COVID-19 pandemic.
Lauren Jelley, Jordan Douglas, Meaghan O'Neill, Klarysse Berquist, Ana Claasen

medRxiv· July 2024

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Congenital myasthenic syndrome caused by a frameshift insertion mutation in .
Szabolcs Szelinger, Jonida Krate, Keri Ramsey, Samuel P Strom, Perry B Shieh, Ana M Claasen

Neurol Genet· August 2020

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Utilizing RNA and outlier analysis to identify an intronic splice-altering variant in AP4S1 in a sibling pair with progressive spastic paraplegia.
Carmel G McCullough, Szabolcs Szelinger, Newell Belnap, Keri Ramsey, Isabelle Schrauwen, Ana M Claasen

Hum Mutat· February 2020

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Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD).
Lorida Llaci, Keri Ramsey, Newell Belnap, Ana M Claasen, Chris D Balak

Hum Genet· December 2019

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Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder.
Michael J McCarthy, Heather Wei, Caroline M Nievergelt, Andrea Stautland, Adam X Maihofer, Ana Claasen

Neuropsychopharmacology· February 2019

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Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results.
Brittany Gerald, Keri Ramsey, Newell Belnap, Szabolcs Szelinger, Ashley L Siniard, Ana M Claasen

Semin Pediatr Neurol· July 2018

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De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder.
Davor Lessel, Claudia Schob, Sébastien Küry, Margot R F Reijnders, Tamar Harel, Ana Claasen

Am J Hum Genet· January 2018

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De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder.
Davor Lessel, Claudia Schob, Sébastien Küry, Margot R F Reijnders, Tamar Harel, Ana Claasen

Am J Hum Genet· November 2017

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A method to reduce ancestry related germline false positives in tumor only somatic variant calling.
Rebecca F Halperin, John D Carpten, Zarko Manojlovic, Jessica Aldrich, Jonathan Keats, Ana Claasen

BMC Med Genomics· October 2017

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Case Report: Novel mutations in are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disability.
Erika Banuelos, Keri Ramsey, Newell Belnap, Malavika Krishnan, Chris Balak, Ana M Claasen

F1000Res· April 2017

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A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia.
Abby M Moskowitz, Newell Belnap, Ashley L Siniard, Szabolcs Szelinger, Ana M Claasen

Cold Spring Harb Mol Case Stud· September 2016

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Secreted amyloid precursor protein-alpha upregulates synaptic protein synthesis by a protein kinase G-dependent mechanism.
Ana M Claasen, Diane Guévremont, Sara E Mason-Parker, Katie Bourne, Warren P Tate

Neurosci Lett· August 2009

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