CaSpER identifies and visualizes CNV events by integrative analysis of single-cell or bulk RNA-sequencing data von Serin Harmanci, Akdes, Harmanci, Arif O., Zhou, Xiaobo

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Phenotypes and genotypes underlying paradoxical pupillary reaction in children von Khan, Arif O.

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Paradoxical keratitis and dermatitis following adalimumab treatment von Ghali, Noor, Khan, Arif O.

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Juvenile progressive optic atrophy as the presenting feature of biotinidase deficiency, a treatable metabolic disorder von Khan, Arif O

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TurboFold: iterative probabilistic estimation of secondary structures for multiple RNA sequences von Harmanci, Arif O, Sharma, Gaurav, Mathews, David H

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HDAC inhibitors elicit metabolic reprogramming by targeting super-enhancers in glioblastoma models von Nguyen, Trang Thi Thu, Zhang, Yiru, Shang, Enyuan, Shu, Chang, Torrini, Consuelo, Zhao, Junfei, Bianchetti, Elena, Mela, Angeliki, Humala, Nelson, Mahajan, Aayushi, Harmanci, Arif O, Lei, Zhengdeng, Maienschein-Cline, Mark, Quinzii, Catarina M, Westhoff, Mike-Andrew, Karpel-Massler, Georg, Bruce, Jeffrey N, Canoll, Peter, Siegelin, Markus D

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Nanophthalmos in children: morphometric and clinical characterization von Khan, Arif O.

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Outcomes of strabismus surgery in genetically confirmed congenital fibrosis of the extraocular muscles von Khan, Arif O.

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Genetics of primary glaucoma von Khan, Arif O

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Presumed uremic optic neuropathy in a patient with Senior-Loken syndrome von Khan, Arif O

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Full-field electroretinography - when do we need it? von Khan, Arif O

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ADAMTS18 -related anterior segment dysgenesis mistaken as Axenfeld-Rieger syndrome von Khan, Arif O

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Inherited retinal diseases and gene therapy update von Khan, Arif O

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COL4A1 MUTATIONS IN TWO INFANTS WITH CONGENITAL CATARACTS AND PORENCEPHALY: AN OPHTHALMOLOGIC PERSPECTIVE von Khan, Arif O.

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Considerations in multi-gene panel testing in pediatric ophthalmology von Khan, Arif O.

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Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocation, Anterior-Segment Abnormalities, and Spontaneous Filtering Blebs, or Traboulsi Syndrome von Patel, Nisha, Khan, Arif O., Mansour, Ahmad, Mohamed, Jawahir Y., Al-Assiri, Abdullah, Haddad, Randa, Jia, Xiaofei, Xiong, Yong, Mégarbané, André, Traboulsi, Elias I., Alkuraya, Fowzan S.

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Fundus autofluorescence imaging in hereditary retinal diseases von Pichi, Francesco, Abboud, Emad B., Ghazi, Nicola G., Khan, Arif O.

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PMEL is mutated in oculocutaneous albinism von AlAbdi, Lama, Alshammari, Muneera, Helaby, Rana, Khan, Arif O., Alkuraya, Fowzan S.

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Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes von Abu-Safieh, Leen, Alrashed, May, Anazi, Shamsa, Alkuraya, Hisham, Khan, Arif O, Al-Owain, Mohammed, Al-Zahrani, Jawahir, Al-Abdi, Lama, Hashem, Mais, Al-Tarimi, Salwa, Sebai, Mohammed-Adeeb, Shamia, Ahmed, Ray-Zack, Mohamed D, Nassan, Malik, Al-Hassnan, Zuhair N, Rahbeeni, Zuhair, Waheeb, Saad, Alkharashi, Abdullah, Abboud, Emad, Al-Hazzaa, Selwa A F, Alkuraya, Fowzan S

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Anterior segment dysgenesis: Insights into the genetics and pathogenesis von Kaushik, Sushmita, Dubey, Suneeta, Choudhary, Sandeep, Ratna, Ria, Pandav, Surinder, Khan, Arif

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