Publications by authors named "Reese Martin"

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Pleiotropy increases with gene age in six model multicellular eukaryotes.
Reese Martin, Ann T Tate

Evol Lett· October 2025

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Relationship Between Brain Activity and Impaired Consciousness in Frontal Lobe Seizures.
Elaheh Salardini, Aparna Vaddiparti, Avisha Kumar, Jiayin Qu, Reese Alan Martin

Neurology· September 2025

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Geno4ME Study: implementation of whole genome sequencing for population screening in a large healthcare system.
Isabelle A Lucas Beckett, Kate R Emery, Josiah T Wagner, Kathleen Jade, Benjamin A Cosgrove, Martin G Reese

NPJ Genom Med· July 2025

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MPSE identifies newborns for whole genome sequencing within 48 h of NICU admission.
Bennet Peterson, Edwin F Juarez, Barry Moore, Edgar Javier Hernandez, Erwin Frise, Martin Tristani-Firouzi, Martin G Reese

NPJ Genom Med· June 2025

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Pleiotropy increases with gene age in six model multicellular eukaryotes.
Reese Martin, Ann T Tate

bioRxiv· November 2024

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Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signalling networks.
Reese A Martin, Ann T Tate

Proc Biol Sci· June 2024

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Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks.
Reese Martin, Ann T Tate

bioRxiv· October 2023

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Response to Grosse et al.
Stephen F Kingsmore, Laurie D Smith, Chris M Kunard, Matthew Bainbridge, Sergey Batalov, Martin G Reese

Am J Hum Genet· June 2023

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Pleiotropy promotes the evolution of inducible immune responses in a model of host-pathogen coevolution.
Reese A Martin, Ann T Tate

PLoS Comput Biol· April 2023

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A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases.
Stephen F Kingsmore, Laurie D Smith, Chris M Kunard, Matthew Bainbridge, Sergey Batalov, Martin G Reese

Am J Hum Genet· September 2022

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An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases.
Mallory J Owen, Sebastien Lefebvre, Christian Hansen, Chris M Kunard, David P Dimmock, Martin G Reese

Nat Commun· July 2022

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Simulated driving in the epilepsy monitoring unit: Effects of seizure type, consciousness, and motor impairment.
Avisha Kumar, Reese Martin, William Chen, Andrew Bauerschmidt, Mark W Youngblood

Epilepsia· January 2022

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Short-term changes in cortical physiological arousal measured by electroencephalography during thalamic centromedian deep brain stimulation.
Reese A Martin, Arthur Cukiert, Hal Blumenfeld

Epilepsia· November 2021

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100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.

N Engl J Med· November 2021

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Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases.
Francisco M De La Vega, Shimul Chowdhury, Barry Moore, Erwin Frise, Jeanette McCarthy, Martin G Reese

Genome Med· October 2021

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Cortical low-frequency power correlates with behavioral impairment in animal model of focal limbic seizures.
Abhijeet Gummadavelli, Reese Martin, Derek Goshay, Lim-Anna Sieu, Jingwen Xu

Epilepsia· August 2021

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Up and Down States of Cortical Neurons in Focal Limbic Seizures.
Zongwei Yue, Isaac G Freedman, Peter Vincent, John P Andrews, Christopher Micek, Reese Martin

Cereb Cortex· May 2020

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Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation.
Michelle M Clark, Amber Hildreth, Sergey Batalov, Yan Ding, Shimul Chowdhury, Martin G Reese

Sci Transl Med· April 2019

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Development of DNA confirmatory and high-risk diagnostic testing for newborns using targeted next-generation DNA sequencing.
Arindam Bhattacharjee, Tanya Sokolsky, Stacia K Wyman, Martin G Reese, Erik Puffenberger

Genet Med· May 2015

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A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.
Hao Hu, Jared C Roach, Hilary Coon, Stephen L Guthery, Karl V Voelkerding, Martin G Reese

Nat Biotechnol· July 2014

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Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear families.
Marc V Singleton, Stephen L Guthery, Karl V Voelkerding, Karin Chen, Brett Kennedy, Martin G Reese

Am J Hum Genet· April 2014

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Using VAAST to Identify Disease-Associated Variants in Next-Generation Sequencing Data.
Brett Kennedy, Zev Kronenberg, Hao Hu, Barry Moore, Steven Flygare, Martin G Reese

Curr Protoc Hum Genet· April 2014

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An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
Catherine A Brownstein, Alan H Beggs, Nils Homer, Barry Merriman, Timothy W Yu, Martin Braun, Martin G Reese

Genome Biol· March 2014

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Integrating precision medicine in the study and clinical treatment of a severely mentally ill person.
Jason A O'Rawe, Han Fang, Shawn Rynearson, Reid Robison, Edward S Kiruluta, Martin G Reese

PeerJ· October 2013

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Clinical analysis of genome next-generation sequencing data using the Omicia platform.
Emily M Coonrod, Rebecca L Margraf, Archie Russell, Karl V Voelkerding, Martin G Reese

Expert Rev Mol Diagn· July 2013

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