Items for Gilks, William

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Number of items: 15.

Article

Gilks, William P (2016) Sex differences in disease genetics. eLS. ISSN 1618-0240

Gilks, William P, Pennell, Tanya M, Flis, Ilona, Webster, Matthew T and Morrow, Edward H (2016) Whole genome resequencing of a laboratory-adapted Drosophila melanogaster population sample. F1000Research, 5. a2644. ISSN 2046-1402

Gilks, William P, Abbott, Jessica K and Morrow, Edward H (2014) Sex differences in disease genetics: evidence, evolution, and detection. Trends in Genetics, 30 (10). pp. 453-463. ISSN 0168-9525

Gilks, William P, Abbott, Jessica K and Morrow, Edward H (2014) Sex differences in disease genetics: evidence, evolution, and detection. Trends in Genetics, 30 (10). pp. 453-463. ISSN 0168-9525

Gilks, William P, Hill, Matthew, Gill, Michael, Donohoe, Gary, Corvin, Aiden P and Morris, Derek W (2012) Functional investigation of a schizophrenia GWAS signal at the CDC42 gene. The World Journal of Biological Psychiatry, 13 (7). pp. 550-554. ISSN 1562-2975

Kenny, Elaine M, Cormican, Paul, Gilks, William P, Gates, Amy S, O'Dushlaine, Colm T, Pinto, Carlos, Corvin, Aiden P, Gill, Michael and Morris, Derek W (2011) Multiplex target enrichment using DNA indexing for ultra-high throughput SNP detection. DNA Research, 18 (1). pp. 31-38. ISSN 1756-1663

Gilks, William P, Allott, Emma H, Donohoe, Gary, Cummings, Elizabeth, International Schizophrenia Consortium, , Gill, Michael, Corvin, Aiden P and Morris, Derek W (2010) Replicated genetic evidence supports a role for HOMER2 in schizophrenia. Neuroscience letters, 468 (3). pp. 229-233. ISSN 1872-7972

Gilks, William P, Abou-Sleiman, Patrick M, Gandhi, Sonia, Jain, Shushant, Singleton, Andrew, Lees, Andrew J, Shaw, Karen, Bhatia, Kailash P, Bonifati, Vincenzo, Quinn, Niall P, Lynch, John, Healy, Daniel G, Holton, Janice L, Revesz, Tamas and Wood, Nicholas W (2005) A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet, 365 (9457). pp. 415-416. ISSN 1474-547X

Valente, Enza Maria, Abou-Sleiman, Patrick M, Caputo, Viviana, Muqit, Miratul M K, Harvey, Kirsten, Gispert, Suzana, Ali, Zeeshan, Del Turco, Domenico, Bentivoglio, Anna Rita, Healy, Daniel G, Albanese, Alberto, Nussbaum, Robert, González-Maldonado, Rafael, Deller, Thomas, Salvi, Sergio, Cortelli, Pietro, Gilks, William P, Latchman, David S, Harvey, Robert J, Dallapiccola, Bruno, Auburger, Georg and Wood, Nicholas W (2004) Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science, 304 (5674). pp. 1158-60. ISSN 1095-9203

Dataset

Gilks, William P, Pennell, Tanya M, Flis, Ilona and Webster, Matthew T (2016) Genotype reproducibility testing in next-generation sequencing data. [Dataset]

Gilks, William (2016) Graphing and tabulating next-generation sequencing and genotyping data. [Dataset]

Gilks, William (2016) Read-mapping for next-generation sequencing data (Wolbachia). [Dataset]

Gilks, William (2016) Structural variant discovery and genotyping in next-generation sequencing data. [Dataset]

Gilks, William (2016) Read-mapping for next-generation sequencing data (Drosophila melanogaster). [Dataset]

Gilks, William (2016) SNP and indel discovery and genotyping in next-generation sequencing data. [Dataset]

This list was generated on Thu Apr 27 14:35:00 2017 BST.