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You searched for: Author/Creator Hicks, Andrew A.

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1. Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly. (March 2019)

2. Deregulation of miRNAs 103a, 30b and 29a in peripheral blood of L-dopa treated Parkinson's patients. (January 2016)

3. Genomewide meta‐analysis identifies loci associated with IGF‐I and IGFBP‐3 levels with impact on age‐related traits. Issue 5 (21st June 2016)

4. Importance of Different Types of Prior Knowledge in Selecting Genome‐Wide Findings for Follow‐Up. Issue 2 (10th January 2013)

7. Large-scale assessment of polyglutamine repeat expansions in Parkinson disease. (13th October 2015)

8. Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Issue 3 (September 2017)

9. PLA2G6 mutations and Parkinsonism: Long‐term follow‐up of clinical features and neuropathology. Issue 12 (6th October 2016)

10. Primary familial brain calcification in the 'IBGC2' kindred: All linkage roads lead to SLC20A2. Issue 12 (27th September 2016)