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1

Infantile Nephropathic Cystinosis: A Novel CTNS Mutation:

Aldahmesh, Mohammed ; Döneray, Hakan ; Orbak, Zerrin..
cd558bbd-5471-478c-bfd3-da72e461041c. , 2017

Link: https://doi.org/10.5152/..

2

Infantile Nephropathic Cystinosis: A Novel CTNS Mutation:

Doneray, Hakan ; Aldahmesh, Mohammed ; Yilmaz, Gulsah..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469843/. , 2017

Link: http://www.ncbi.nlm.nih...

3

Characterizing the morbid genome of ciliopathies:

Shaheen, Ranad ; Szymanska, Katarzyna ; Basu, Basudha...
http://genomebiology.com/2016/17/1/242. , 2016

Link: http://genomebiology.com..

4

Novel phenotypes and loci identified through clinical genom..:

Patel, Nisha ; Anand, Deepti ; Monies, Dorota...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783298/. , 2016

Link: http://www.ncbi.nlm.nih...

5

Phenotypes of Recessive Pediatric Cataract in a Cohort of C..:

Khan, Arif O ; Aldahmesh, Mohammed A ; Alkuraya, Fowzan S
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634221/. , 2015

Link: http://www.ncbi.nlm.nih...

6

An siRNA-based functional genomics screen for the identific..:

Wheway, Gabrielle ; Schmidts, Miriam ; Mans, Dorus A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536769/. , 2015

Link: http://www.ncbi.nlm.nih...

7

Mutations in LRPAP1 Are Associated with Severe Myopia in Hu..:

Aldahmesh, Mohammed A ; Khan, Arif O ; Alkuraya, Hisham...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738831. , 2013

Link: http://www.ncbi.nlm.nih...

8

Mutations in C12orf57 Cause a Syndromic Form of Colobomatou..:

Zahrani, Fatema ; Aldahmesh, Mohammed A ; Alshammari, Muneera J..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591839. , 2013

Link: http://www.ncbi.nlm.nih...

9

Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectua..:

Aldahmesh, Mohammed A ; Mohamed, Jawahir Y ; Alkuraya, Hisham S...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234380. , 2011

Link: http://www.ncbi.nlm.nih...

10

Novel mutations in MERTK associated with childhood onset ro..:

Mackay, Donna S ; Henderson, Robert H ; Sergouniotis, Panagiotis I...
qt0037f4t1. , 2010

Link: https://escholarship.org..

11

MeltMADGE for mutation scanning of specific genes in popula..:

Alharbi, Khalid K ; Aldahmesh, Mohammed A ; Gaunt, Tom R...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575632. , 2010

Link: http://www.ncbi.nlm.nih...

12

The enhanced S‐cone syndrome in children:

Khan, Arif O ; Aldahmesh, Mohammed ; Meyer, Brian
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1857689. , 2007

Link: http://www.ncbi.nlm.nih...

13

Mutation scanning by meltMADGE: Validations using BRCA1 and..:

Alharbi, Khalid K ; Aldahmesh, Mohammed A ; Spanakis, Emmanuel...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1172041. , 2005

Link: http://www.ncbi.nlm.nih...

14

Accelerating Novel Candidate Gene Discovery in Neurogenetic..:

Anas M. Alazami ; Nisha Patel ; Hanan E. Shamseldin...
http://www.sciencedirect.com/science/article/pii/S2211124714010444. , 2015

Link: https://doi.org/10.1016/..

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