Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes von Dunn, Paul, Albury, Cassie L, Maksemous, Neven, Benton, Miles C, Sutherland, Heidi G, Smith, Robert A, Haupt, Larisa M, Griffiths, Lyn R

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Discriminating head trauma outcomes using machine learning and genomics von Ibrahim, Omar, Sutherland, Heidi G., Lea, Rodney A., Nasrallah, Fatima, Maksemous, Neven, Smith, Robert A., Haupt, Larisa M., Griffiths, Lyn R.

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Eye movement disorders are an early manifestation of CACNA1A mutations in children von Tantsis, Esther M, Gill, Deepak, Griffiths, Lyn, Gupta, Sachin, Lawson, John, Maksemous, Neven, Ouvrier, Robert, Riant, Florence, Smith, Robert, Troedson, Christopher, Webster, Richard, Menezes, Manoj P

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Tiered analysis of whole-exome sequencing for epilepsy diagnosis von Dunn, Paul J., Maher, Bridget H., Albury, Cassie L., Stuart, Shani, Sutherland, Heidi G., Maksemous, Neven, Benton, Miles C., Smith, Robert A., Haupt, Larisa M., Griffiths, Lyn R.

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P609: Improving genome diagnostics of hemiplegic migraine von Al-Fayyadh, Mohammed, Maksemous, Neven, Sutherland, Heidi, Lea, Rod, Griffiths, Lyn

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Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity von Maksemous, Neven, Smith, Robert A, Sutherland, Heidi G, Sampaio, Hugo, Griffiths, Lyn R

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Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine von Maksemous, Neven, Blayney, Claire D, Sutherland, Heidi G, Smith, Robert A, Lea, Rod A, Tran, Kim Ngan, Ibrahim, Omar, McArthur, Jeffrey R, Haupt, Larisa M, Cader, M Zameel, Finol-Urdaneta, Rocio K, Adams, David J, Griffiths, Lyn R

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Exome Sequencing Diagnoses X-Linked Moesin-Associated Immunodeficiency in a Primary Immunodeficiency Case von Bradshaw, Gabrielle, Lualhati, Robbie R, Albury, Cassie L, Maksemous, Neven, Roos-Araujo, Deidre, Smith, Robert A, Benton, Miles C, Eccles, David A, Lea, Rod A, Sutherland, Heidi G, Haupt, Larisa M, Griffiths, Lyn R

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Novel compound heterozygous missense mutations in GDAP1 cause Charcot–Marie–Tooth type 4A von XUE, HUIQIN, MAKSEMOUS, NEVEN, SIDHOM, DAVID, MA, LAN, CHEN, SHAOHUI, WU, JIANRUI, FENG, YU, HAUPT, LARISA M., GRIFFITHS, LYN R.

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Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants von Sutherland, Heidi G., Maksemous, Neven, Albury, Cassie L., Ibrahim, Omar, Smith, Robert A., Lea, Rod A., Haupt, Larisa M., Jenkins, Bronwyn, Tsang, Benjamin, Griffiths, Lyn R.

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Comprehensive Exonic Sequencing of Known Ataxia Genes in Episodic Ataxia von Maksemous, Neven, Sutherland, Heidi G., Smith, Robert A., Haupt, Larisa M., Griffiths, Lyn R.

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Next‐generation sequencing identifies novel CACNA1A gene mutations in episodic ataxia type 2 von Maksemous, Neven, Roy, Bishakha, Smith, Robert A., Griffiths, Lyn R.

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Targeted next generation sequencing identifies a genetic spectrum of DNA variants in patients with hemiplegic migraine von Maksemous, Neven, Smith, Robert A, Sutherland, Heidi G, Maher, Bridget H, Ibrahim, Omar, Nicholson, Garth A, Carpenter, Elisabeth P, Lea, Rod A, Cader, M Zameel, Griffiths, Lyn R

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Genome Sequencing in Esophageal Squamous Cell Carcinoma von Pillai, Suja, Maksemous, Neven, Lam, Alfred K.

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PathVar: A Customisable NGS Variant Calling Algorithm Implicates Novel Candidate Genes and Pathways in Hemiplegic Migraine von Alfayyadh, Mohammed M, Maksemous, Neven, Sutherland, Heidi G, Lea, Rodney A, Griffiths, Lyn R

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Exploring Neuronal Vulnerability to Head Trauma Using a Whole Exome Approach von Ibrahim, Omar, Sutherland, Heidi G., Maksemous, Neven, Smith, Robert, Haupt, Larisa M., Griffiths, Lyn R.

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Investigating a Genetic Link Between Alzheimer’s Disease and CADASIL-Related Cerebral Small Vessel Disease von Dunn, Paul J., Lea, Rodney A., Maksemous, Neven, Smith, Robert A., Sutherland, Heidi G., Haupt, Larisa M., Griffiths, Lyn R.

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Exonic mutations in cell–cell adhesion may contribute to CADASIL-related CSVD pathology von Dunn, Paul J., Lea, Rodney A., Maksemous, Neven, Smith, Robert A., Sutherland, Heidi G., Haupt, Larisa M., Griffiths, Lyn R.

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Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging Approaches von Alfayyadh, Mohammed M, Maksemous, Neven, Sutherland, Heidi G, Lea, Rod A, Griffiths, Lyn R

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Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes von Maksemous, Neven, Harder, Aster V. E., Ibrahim, Omar, Vijfhuizen, Lisanne S., Sutherland, Heidi, Pelzer, Nadine, de Boer, Irene, Terwindt, Gisela M., Lea, Rodney A., van den Maagdenberg, Arn M. J. M., Griffiths, Lyn R.

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