Publications by authors named "Laina Lusk"

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"Living with" -related hemiplegic migraine, a disease concept model.
Donna Schaare, Kendra Allison, Kara Skorge, Pangkong Fox, Laina Lusk, Sara M Sarasua, Ingo Helbig, Luigi Boccuto

Front Neurol· November 2024

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Characterization of the functional and clinical impacts of missense variants found in neurodevelopmental disorders.
Erkin Kurganov, Lei Cui, Nikita Budnik, Siwei Chen, Erick Olivares, Laina Lusk

Sci Transl Med· December 2025

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Phenotypic analysis of 11,125 trio exomes in neurodevelopmental disorders.
Shiva Ganesan, Sarah M Ruggiero, Shridhar Parthasarathy, Peter D Galer, David Lewis-Smith, Laina Lusk

bioRxiv· March 2025

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A Longitudinal Exploration of -Related Hemiplegic Migraine in Children Using Electronic Medical Records.
Donna Schaare, Laina Lusk, Alexis Karlin, Michael C Kaufman, Jan Magielski

Neurol Genet· February 2025

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Expanding Genetic Counselor Roles: A Model for Global Research Development.
Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart, T Blaine Crowley, Stephanie Asher, Laina Lusk

Genes (Basel)· July 2024

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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Maimuna S Paul, Sydney L Michener, Hongling Pan, Hiuling Chan, Jessica M Pfliger, Laina Lusk

Am J Hum Genet· June 2024

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A Longitudinal Exploration of -related Hemiplegic Migraine in Children.
Donna Schaare, Laina Lusk, Alexis Karlin, Michael C Kaufman, Jan Magielski

medRxiv· June 2024

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Developmental epileptic encephalopathy in DLG4-related synaptopathy.
Benedetta Kassabian, Amanda M Levy, Elena Gardella, Angel Aledo-Serrano, Amitha L Ananth, Laina Lusk

Epilepsia· April 2024

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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Maimuna S Paul, Sydney L Michener, Hongling Pan, Hiuling Chan, Jessica M Pfliger, Laina Lusk

Am J Hum Genet· April 2024

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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Maimuna S Paul, Sydney L Michener, Hongling Pan, Hiuling Chan, Jessica M Pfliger, Laina Lusk

Am J Hum Genet· January 2024

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Segmenting Speech by Mouth: The Role of Oral Prosodic Cues for Visual Speech Segmentation.
Aaron D Mitchel, Laina G Lusk, Ian Wellington, Alexis T Mook

Lang Speech· December 2023

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Genetic variants in contribute to Autism Spectrum Disorder associated with the Xp22.11 locus.
Marcello Scala, Clarrisa A Bradley, Jennifer L Howe, Brett Trost, Nelson Bautista Salazar, Laina Lusk

medRxiv· December 2023

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Corrigendum: Intrafamilial variability in -related neurodevelopmental disorders.
Benedetta Kassabian, Christina Dühring Fenger, Marjolaine Willems, Angel Aledo-Serrano, Tarja Linnankivi, Laina Lusk

Front Neurosci· August 2023

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Intrafamilial variability in -related neurodevelopmental disorders.
Benedetta Kassabian, Christina Dühring Fenger, Marjolaine Willems, Angel Aledo-Serrano, Tarja Linnankivi, Laina Lusk

Front Neurosci· July 2023

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Rare variants in cause delayed development, intellectual disability, autism, and epilepsy.
Maimuna S Paul, Sydney L Michener, Hongling Pan, Jessica M Pfliger, Jill A Rosenfeld, Laina Lusk

medRxiv· March 2023

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Concomitant Calcium Channelopathies Involving and A Case Report and Review of the Literature.
Donna Schaare, Sara M Sarasua, Laina Lusk, Shridhar Parthasarathy, Liangjiang Wang

Genes (Basel)· February 2023

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A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism.
Shridhar Parthasarathy, Sarah McKeown Ruggiero, Antoinette Gelot, Fernanda C Soardi, Bethânia F R Ribeiro, Laina Lusk

Am J Hum Genet· December 2022

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Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature.
Jessica R C Priestley, Lisa M Pace, Kuntal Sen, Anjali Aggarwal, Cesar Augusto P F Alves, Laina Lusk

Mol Genet Metab Rep· December 2022

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Segregation of two variants suggests the presence of autosomal dominant and recessive forms of -related disease within the same family: expanding the phenotypic spectrum of Wolfram Syndrome.
Laina Lusk, Emily Black, Jaime Vengoechea

J Med Genet· February 2020

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Dimensional assessment of schizotypal, psychotic, and other psychiatric traits in children and their parents: development and validation of the Childhood Oxford-Liverpool Inventory of Feelings and Experiences on a representative US sample.
David W Evans, Laina G Lusk, Mylissa M Slane, Andrew M Michael, Scott M Myers

J Child Psychol Psychiatry· May 2018

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Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early Uses.
Oluwaseun Jessica Ajayi, Ebony Jeannae Smith, Teeradache Viangteeravat, Eunice Y Huang, Naga Satya V Rao Nagisetty, Laina Lusk

JMIR Res Protoc· October 2017

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Development of Two Dimensional Measures of Restricted and Repetitive Behavior in Parents and Children.
David W Evans, Mirko Uljarević, Laina G Lusk, Eva Loth, Thomas Frazier

J Am Acad Child Adolesc Psychiatry· January 2017

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