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Clokie, Samuel J.
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1

Genetic Diagnosis of Retinoblastoma Using Aqueous Humour—Fi..:

Gerrish, Amy ; Mashayamombe-Wolfgarten, Chipo ; Stone, Edward...
Cancers.  16 (2024)  8 - p. 1565 , 2024
Link: https://doi.org/10.3390/..
 
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2

Analysis of Fibroblast Growth Factor 14 (FGF14) structural ..:

Ceroni, Fabiola ; Osborne, Daniel ; Clokie, Samuel...
European Journal of Human Genetics.  31 (2022)  3 - p. 353-359 , 2022
Link: https://doi.org/10.1038/..
 
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3

Clinical Service Delivery of Noninvasive Prenatal Diagnosis..:

Young, Elizabeth ; Bowns, Benjamin ; Gerrish, Amy...
The Journal of Molecular Diagnostics.  22 (2020)  9 - p. 1151-1161 , 2020
Link: https://doi.org/10.1016/..
 
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4

Resource: A multi‐species multi‐timepoint transcriptome dat..:

Chang, Eric ; Fu, Cong ; Coon, Steven L....
Journal of Pineal Research.  69 (2020)  3 - p. , 2020
Link: https://doi.org/10.1111/..
 
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5

Non-Invasive Prenatal Diagnosis of Retinoblastoma Inheritan..:

Gerrish, Amy ; Bowns, Benjamin ; Mashayamombe-Wolfgarten, Chipo...
Journal of Clinical Medicine.  9 (2020)  11 - p. 3517 , 2020
Link: https://doi.org/10.3390/..
 
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6

mir-374-5p, mir-379-5p, and mir-503-5p Regulate Proliferati..:

Jee, Youn Hee ; Wang, Jinhee ; Yue, Shanna...
Endocrinology.  159 (2018)  3 - p. 1469-1478 , 2018
Link: https://doi.org/10.1210/..
 
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7

Non-invasive prenatal diagnosis of spinal muscular atrophy ..:

Parks, Michael ; Court, Samantha ; Bowns, Benjamin...
European Journal of Human Genetics.  25 (2017)  4 - p. 416-422 , 2017
Link: https://doi.org/10.1038/..
 
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8

Increased Sensitivity of Diagnostic Mutation Detection by R..:

Watson, Christopher M. ; Camm, Nick ; Crinnion, Laura A....
Molecular Diagnosis & Therapy.  21 (2017)  6 - p. 685-692 , 2017
Link: https://doi.org/10.1007/..
 
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9

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Typ..:

Watson, Lauren M. ; Bamber, Elizabeth ; Schnekenberg, Ricardo Parolin...
The American Journal of Human Genetics.  101 (2017)  5 - p. 866 , 2017
Link: https://doi.org/10.1016/..
 
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10

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Typ..:

Watson, Lauren M. ; Bamber, Elizabeth ; Schnekenberg, Ricardo Parolin...
The American Journal of Human Genetics.  101 (2017)  3 - p. 451-458 , 2017
Link: https://doi.org/10.1016/..
 
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11

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Typ..:

Watson, Lauren M. ; Bamber, Elizabeth ; Schnekenberg, Ricardo Parolin...
The American Journal of Human Genetics.  101 (2017)  4 - p. 638 , 2017
Link: https://doi.org/10.1016/..
 
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12

Non‐invasive prenatal diagnosis of Duchenne and Becker musc..:

Parks, Michael ; Court, Samantha ; Cleary, Siobhan...
Prenatal Diagnosis.  36 (2016)  4 - p. 312-320 , 2016
Link: https://doi.org/10.1002/..
 
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13

Chronic FLT3-ITD Signaling in Acute Myeloid Leukemia Is Con..:

Cauchy, Pierre ; James, Sally R. ; Zacarias-Cabeza, Joaquin...
Cell Reports.  12 (2015)  5 - p. 821-836 , 2015
Link: https://doi.org/10.1016/..
 
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14

Molecular Signatures of Mouse TRPV1-Lineage Neurons Reveale..:

Goswami, Samridhi C. ; Mishra, Santosh K. ; Maric, Dragan...
The Journal of Pain.  15 (2014)  12 - p. 1338-1359 , 2014
Link: https://doi.org/10.1016/..
 
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15

The Lhx9 homeobox gene controls pineal gland development an..:

Yamazaki, Fumiyoshi ; Møller, Morten ; Fu, Cong...
Brain Structure and Function.  220 (2014)  3 - p. 1497-1509 , 2014
Link: https://doi.org/10.1007/..
 
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