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Hand, Collette K.
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1

Low incidence of BRAF and NRAS mutations in a population wi..:

Neville, Grace ; Marzario, Barbara ; Shilling, David..
Virchows Archiv.  484 (2024)  3 - p. 475-479 , 2024
Link: https://doi.org/10.1007/..
 
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2

Implementation of an ISO 15189 accredited next generation s..:

Werner, Reiltin ; Crosbie, Ruth ; Dorney, Mairead...
Journal of Clinical Pathology.  , 2024
Link: https://doi.org/10.1136/..
 
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3

Implementation of an ISO15189 accredited next-generation se..:

Werner, Réiltín ; Connolly, Amy ; Bennett, Michael..
Journal of Clinical Pathology.  77 (2022)  4 - p. 278-283 , 2022
Link: https://doi.org/10.1136/..
 
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4

Mutagenesis by Microbe: the Role of the Microbiota in Shapi..:

Barrett, Maurice ; Hand, Collette K. ; Shanahan, Fergus..
Trends in Cancer.  6 (2020)  4 - p. 277-287 , 2020
Link: https://doi.org/10.1016/..
 
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5

Chorea–Acanthocytosis and the Huntington Disease Allele in ..:

Murphy, Olwen C. ; O'Toole, Orna ; Hand, Collette K..
Tremor and Other Hyperkinetic Movements.  8 (2018)  0 - p. 604 , 2018
Link: https://doi.org/10.5334/..
 
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6

Phenotypic Variation in a Caucasian Kindred with Chorea‐Aca..:

Merwick, Áine ; Mok, Tzehow ; McNamara, Brian...
Movement Disorders Clinical Practice.  2 (2014)  1 - p. 86-89 , 2014
Link: https://doi.org/10.1002/..
 
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7

A novel locus for restless legs syndrome maps to chromosome..:

Skehan, Evelyn B. ; Abdulrahim, Manal M. A. ; Parfrey, Nollaig A..
neurogenetics.  13 (2012)  2 - p. 125-132 , 2012
Link: https://doi.org/10.1007/..
 
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8

A Novel ATP1A2 Gene Mutation in an Irish Familial Hemiplegi..:

Fernandez, Desiree M. ; Hand, Collette K. ; Sweeney, Brian J..
Headache: The Journal of Head and Face Pain.  48 (2007)  1 - p. 101-108 , 2007
Link: https://doi.org/10.1111/..
 
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9

Novel RPGR mutations with distinct retinitis pigmentosa phe..:

Koenekoop, Robert K ; Loyer, Magali ; Hand, Collette K...
American Journal of Ophthalmology.  136 (2003)  4 - p. 678-687 , 2003
Link: https://doi.org/10.1016/..
 
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10

An ALS2 gene mutation causes hereditary spastic paraplegia ..:

Gros‐Louis, François ; Meijer, Inge A. ; Hand, Collette K....
Annals of Neurology.  53 (2002)  1 - p. 144-145 , 2002
Link: https://doi.org/10.1002/..
 
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11

Familial amyotrophic lateral sclerosis:

Hand, Collette K. ; Rouleau, Guy A.
Muscle & Nerve.  25 (2002)  2 - p. 135-159 , 2002
Link: https://doi.org/10.1002/..
 
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12

Compound heterozygous D90A and D96N SOD1 mutations in a rec..:

Hand, Collette K. ; Mayeux-Portas, Veronique ; Khoris, Jawad...
Annals of Neurology.  49 (2001)  2 - p. 267-271 , 2001
Link: https://doi.org/10.1002/..
 
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13

Reply:

Hand, Collette K. ; Mayeux‐Portas, Veronique ; Khoris, Jawad...
Annals of Neurology.  50 (2001)  4 - p. 554-554 , 2001
Link: https://doi.org/10.1002/..
 
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14

A gene encoding a putative GTPase regulator is mutated in f..:

Hadano, Shinji ; Hand, Collette K. ; Osuga, Hitoshi...
Nature Genetics.  29 (2001)  2 - p. 166-173 , 2001
Link: https://doi.org/10.1038/..
 
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15

Localization of the Gene for Autosomal Recessive Congenital..:

Hand, Collette K. ; Harmon, Dawn L. ; Kennedy, Susan M....
Genomics.  61 (1999)  1 - p. 1-4 , 1999
Link: https://doi.org/10.1006/..
 
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