1.
Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocation, Anterior-Segment Abnormalities, and Spontaneous Filtering Blebs, or Traboulsi Syndrome
by Patel, Nisha
American journal of human genetics, 2014-05-01, Vol.94 (5), p.755-759
2.
Decreased suicide rates in recent antidepressant clinical trials
by Khan, Arif
Psychopharmacology, 2018-02-26, Vol.235 (5), p.1455-1462
3.
Mutations in LRPAP1 Are Associated with Severe Myopia in Humans
by Aldahmesh, Mohammed A
American journal of human genetics, 2013-08-08, Vol.93 (2), p.313-320
4.
How a Psychopharmacology Clinical Trial Site in the Seattle Area Managed Clinical Trials and Patient Care During the COVID-19 Pandemic
by Schilling, Shirin
The American journal of geriatric psychiatry, 2020-09, Vol.28 (9), p.999-1003
5.
Long-Term Safety and Efficacy of Subcutaneous Methylnaltrexone in Patients with Opioid-Induced Constipation and Chronic Noncancer Pain: A Phase 3, Open-Label Trial
by Webster, Lynn R
Pain medicine (Malden, Mass.), 2017-08-01, Vol.18 (8), p.1496-1504
6.
C21orf2 is mutated in recessive early-onset retinal dystrophy with macular staphyloma and encodes a protein that localises to the photoreceptor primary cilium
by Khan, Arif O
British journal of ophthalmology, 2015-12, Vol.99 (12), p.1725-1731
7.
Magnitude of change with antidepressants and placebo in antidepressant clinical trials using structured, taped and appraised rater interviews (SIGMA-RAPS) compared to trials using...
by Khan, Arif
Psychopharmacology, 2014-04-26, Vol.231 (22), p.4301-4307
8.
Outcomes of Ahmed Glaucoma Valve Revision in Pediatric Glaucoma
by Al-Omairi, Ahmed Mansour
American journal of ophthalmology, 2017-11, Vol.183, p.141-146
9.
A TULP1 founder mutation, p.Gln301, underlies a recognisable congenital rod–cone dystrophy phenotype on the Arabian Peninsula
by Khan, Arif O
British journal of ophthalmology, 2015-04, Vol.99 (4), p.488-492
10.
Recessive Mutations in COL25A1 Are a Cause of Congenital Cranial Dysinnervation Disorder
by Shinwari, Jameela M.A
American journal of human genetics, 2015-01-08, Vol.96 (1), p.147-152
11.
GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome
by Patel, Nisha
American journal of human genetics, 2017-05-04, Vol.100 (5), p.831-836
12.
Resveratrol suppresses the proliferation of breast cancer cells by inhibiting fatty acid synthase signaling pathway
by Khan, Arif
Cancer epidemiology, 2014, Vol.38 (6), p.765-772
13.
Clinical characterisation of the CABP4-related retinal phenotype
by Khan, Arif O
British journal of ophthalmology, 2013-03, Vol.97 (3), p.262-265
14.
Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish
by Van De Weghe, Julie C
American journal of human genetics, 2017-07-06, Vol.101 (1), p.23-36
15.
Genetic analysis of strictly defined Leber congenital amaurosis with (and without) neurodevelopmental delay
by Khan, Arif O
British journal of ophthalmology, 2014-12, Vol.98 (12), p.1724-1728
16.
‘Cone dystrophy with supranormal rod response’ in children
by Khan, Arif O
British journal of ophthalmology, 2012-03, Vol.96 (3), p.422-426
17.
The distinct ophthalmic phenotype of Knobloch syndrome in children
by Khan, Arif O
British journal of ophthalmology, 2012-06, Vol.96 (6), p.890-895
18.
Ophthalmic features of PLA2G6-related paediatric neurodegeneration with brain iron accumulation
by Khan, Arif O
British journal of ophthalmology, 2014-07, Vol.98 (7), p.889-893
19.
Biometric and Molecular Characterization of Clinically Diagnosed Posterior Microphthalmos
by Nowilaty, Sawsan R
American journal of ophthalmology, 2013, Vol.155 (2), p.361-372.e7
20.
Identification of ADAMTS18 as a gene mutated in Knobloch syndrome
by Aldahmesh, Mohammed A
Journal of medical genetics, 2011-09, Vol.48 (9), p.597-601
