Publications by authors named "Alexander Drew"

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Carbapenemase-producing non-typhoidal salmonellae: do we need to standardise algorithms for susceptibility testing in routine practice?
Samuel W L Baumgart, Anne Watt, Geraldine Sullivan, Alexander Drew, Basel Suliman

Pathology· September 2025

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A laboratory framework for ongoing optimization of amplification-based genomic surveillance programs.
Connie Lam, Jessica Johnson-Mackinnon, Kerri Basile, Winkie Fong, Carl J E Suster, Alexander Drew

Microbiol Spectr· December 2023

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Considerations for using a removable prosthesis with attachments for a staged approach to a failing implant reconstruction.
Mohammed S Murayshed, Jason Kim, Howard Drew, Alexander Drew

Quintessence Int· February 2023

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Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis.
Lisa J Ewans, Andre E Minoche, Deborah Schofield, Rupendra Shrestha, Clare Puttick, Alexander Drew

Eur J Hum Genet· October 2022

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Guiding the design of SARS-CoV-2 genomic surveillance by estimating the resolution of outbreak detection.
Carl J E Suster, Alicia Arnott, Grace Blackwell, Mailie Gall, Jenny Draper, Alexander P Drew

Front Public Health· October 2022

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Co-infection with SARS-CoV-2 Omicron and Delta variants revealed by genomic surveillance.
Rebecca J Rockett, Jenny Draper, Mailie Gall, Eby M Sim, Alicia Arnott, Alexander P Drew, Andrew N Ginn

Nat Commun· May 2022

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Biallelic AOPEP Loss-of-Function Variants Cause Progressive Dystonia with Prominent Limb Involvement.
Michael Zech, Kishore R Kumar, Sophie Reining, Janine Reunert, Michel Tchan, Alexander P Drew

Mov Disord· January 2022

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Facioscapulohumeral muscular dystrophy type 2: an update on the clinical, genetic, and molecular findings.
Fangzhi Frank Jia, Alexander P Drew, Garth Alexander Nicholson, Alastair Corbett, Kishore Raj Kumar

Neuromuscul Disord· November 2021

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Diagnostic Yield of Whole Genome Sequencing After Nondiagnostic Exome Sequencing or Gene Panel in Developmental and Epileptic Encephalopathies.
Elizabeth Emma Palmer, Rani Sachdev, Rebecca Macintosh, Uirá Souto Melo, Stefan Mundlos, Alexander P Drew, Peter Ian Andrews

Neurology· March 2021

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The Lifeact-EGFP mouse is a translationally controlled fluorescent reporter of T cell activation.
Jorge Luis Galeano Niño, Szun S Tay, Jacqueline L E Tearle, Jianling Xie, Matt A Govendir, Alexander P Drew

J Cell Sci· March 2020

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Fracture Strength of Implant Screw-Retained All-Ceramic Crowns with the Use of the Angulated Screw Channel: A Pilot Study.
Alexander Drew, Anthony Randi, Louis DiPede, Allyn Luke

Int J Periodontics Restorative Dent· February 2020

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Novel intraoperative radiotherapy utilizing prefabricated custom three-dimensionally printed high-dose-rate applicators.
Brandon S Imber, Suzanne L Wolden, Hilda E Stambuk, Evan Matros, Leonard H Wexler, Alexander S Drew

Brachytherapy· December 2019

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Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family.
Shelisa Tey, Nortina Shahrizaila, Alexander P Drew, Sarimah Samulong, Khean-Jin Goh

Neurogenetics· August 2019

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Response to Brodehl et al.
Andre E Minoche, Claire Horvat, Renee Johnson, Velimir Gayevskiy, Sarah U Morton, Alexander P Drew

Genet Med· May 2019

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Oncology Curricula in Postgraduate General Dentistry Programs: a Survey of Residency Program Directors.
Evan B Rosen, Alexander Drew, Joseph M Huryn

J Cancer Educ· April 2019

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De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome.
Elizabeth E Palmer, Seungbeom Hong, Fatema Al Zahrani, Mais O Hashem, Fajr A Aleisa, Alexander P Drew, Marisa V Andrews

Am J Hum Genet· April 2019

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Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy.
Andre E Minoche, Claire Horvat, Renee Johnson, Velimir Gayevskiy, Sarah U Morton, Alexander P Drew

Genet Med· March 2019

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Fabrication of a custom brachytherapy appliance.
Alexander Drew, David H Abramson, Suzanne L Wolden, Marjorie Golden, Joseph Randazzo

J Prosthet Dent· March 2019

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De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-Progressive Neurocognitive Syndrome.
Elizabeth E Palmer, Seungbeom Hong, Fatema Al Zahrani, Mais O Hashem, Fajr A Aleisa, Alexander P Drew, Marisa V Andrews

Am J Hum Genet· March 2019

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Prosthetically Driven Therapy for a Patient With Systemic Lupus Erythematosus and Common Variable Immunodeficiency: A Case Report.
Alexander Drew, Nurit Bittner, Whitney Florin, Alia Koch

J Oral Implantol· December 2018

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Defining the distinct, intrinsic properties of the novel type I interferon, IFNϵ.
Sebastian A Stifter, Antony Y Matthews, Niamh E Mangan, Ka Yee Fung, Alexander Drew

J Biol Chem· March 2018

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A 1.35 Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34-q36.2.
Alexander P Drew, Anthony N Cutrupi, Megan H Brewer, Garth A Nicholson, Marina L Kennerson

Hum Genet· November 2016

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Pathogenic mechanisms underlying X-linked Charcot-Marie-Tooth neuropathy (CMTX6) in patients with a pyruvate dehydrogenase kinase 3 mutation.
Gonzalo Perez-Siles, Carolyn Ly, Adrienne Grant, Alexander P Drew, Eppie M Yiu

Neurobiol Dis· October 2016

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Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3.
Megan H Brewer, Rabia Chaudhry, Jessica Qi, Aditi Kidambi, Alexander P Drew

PLoS Genet· July 2016

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MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs.
Obaid M Albulym, Marina L Kennerson, Matthew B Harms, Alexander P Drew, Anna H Siddell

Ann Neurol· March 2016

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