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Aldahmesh, Mohammed A.
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1

Congenital glaucoma and CYP1B1: an old story revisited:

Alsaif, Hessa S. ; Khan, Arif O. ; Patel, Nisha...
Human Genetics.  138 (2018)  8-9 - p. 1043-1049 , 2018
Link: https://doi.org/10.1007/..
 
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2

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/..
 
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3

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...
 
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4

Congenital hereditary endothelial dystrophy, not glaucoma, ..:

Khan, Arif O. ; Aldahmesh, Mohammed A. ; Alkuraya, Fowzan
Journal of American Association for Pediatric Ophthalmology and Strabismus.  20 (2016)  4 - p. 370-372 , 2016
Link: https://doi.org/10.1016/..
 
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5

Expanding the clinical, allelic, and locus heterogeneity of..:

Patel, Nisha ; Aldahmesh, Mohammed A. ; Alkuraya, Hisham...
Genetics in Medicine.  18 (2016)  6 - p. 554-562 , 2016
Link: https://doi.org/10.1038/..
 
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6

Novel phenotypes and loci identified through clinical genom..:

Patel, Nisha ; Anand, Deepti ; Monies, Dorota...
Human Genetics.  136 (2016)  2 - p. 205-225 , 2016
Link: https://doi.org/10.1007/..
 
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7

Characterizing the morbid genome of ciliopathies:

Ciliopathy WorkingGroup ; Shaheen, Ranad ; Szymanska, Katarzyna...
Genome Biology.  17 (2016)  1 - p. , 2016
Link: https://doi.org/10.1186/..
 
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8

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...
 
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9

Characterizing the morbid genome of ciliopathies:

Shaheen, Ranad ; Szymanska, Katarzyna ; Basu, Basudha...
http://genomebiology.com/2016/17/1/242.  , 2016
Link: http://genomebiology.com..
 
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10

Exome-based case–control association study using extreme ph..:

Shtir, Corina ; Aldahmesh, Mohammed A. ; Al-Dahmash, Saad...
Human Genetics.  135 (2015)  2 - p. 193-200 , 2015
Link: https://doi.org/10.1007/..
 
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11

Accelerating Novel Candidate Gene Discovery in Neurogenetic..:

Alazami, Anas M. ; Patel, Nisha ; Shamseldin, Hanan E....
Cell Reports.  10 (2015)  2 - p. 148-161 , 2015
Link: https://doi.org/10.1016/..
 
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12

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...
 
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13

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...
 
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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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15

Biometric and Molecular Characterization of Clinically Diag..:

Nowilaty, Sawsan R. ; Khan, Arif O. ; Aldahmesh, Mohammed A....
American Journal of Ophthalmology.  155 (2013)  2 - p. 361-372.e7 , 2013
Link: https://doi.org/10.1016/..
 
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