1. Cellular α-synuclein pathology is associated with bioenergetic dysfunction in Parkinson's iPSC-derived dopamine neurons. (11th February 2019) Authors: Zambon, Federico; Cherubini, Marta; Fernandes, Hugo J R; Lang, Charmaine; Ryan, Brent J; Volpato, Viola; Bengoa-Vergniory, Nora; Vingill, Siv; Attar, Moustafa; Booth, Heather D E; Haenseler, Walther; Vowles, Jane; Bowden, Rory; Webber, Caleb; Cowley, Sally A; Wade-Martins, Richard Journal: Human molecular genetics Issue: Volume 28:Number 12(2019) Page Start: 2001 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical Significance of De Novo and Inherited Copy‐Number Variation. Issue 12 (10th October 2013) Authors: Vulto‐van Silfhout, Anneke T.; Hehir‐Kwa, Jayne Y.; van, Bregje W.M.; Schuurs‐Hoeijmakers, Janneke H.M.; Meader, Stephen; Hellebrekers, Claudia J.M.; Thoonen, Ilse J.M.; de, Arjan P.M.; Brunner, Han G.; Webber, Caleb; Pfundt, Rolph; de, Nicole; de, Bert B.A. Journal: Human mutation Issue: Volume 34:Issue 12(2013:Dec.) Page Start: 1679 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Deep phenotyping of peripheral tissue facilitates mechanistic disease stratification in sporadic Parkinson's disease. (April 2020) Authors: Carling, Phillippa J; Mortiboys, Heather; Green, Claire; Mihaylov, Simeon; Sandor, Cynthia; Schwartzentruber, Aurelie; Taylor, Rosie; Wei, Wenbin; Hastings, Chris; Wong, Siew; Lo, Christine; Evetts, Samuel; Clemmens, Hannah; Wyles, Matthew; Willcox, Sam; Payne, Thomas; Hughes, Rachel; Ferraiuolo,... Journal: Progress in neurobiology Issue: Volume 187(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Duplications in ADHD patients harbour neurobehavioural genes that are co‐expressed with genes associated with hyperactivity in the mouse. Issue 2 (5th February 2015) Authors: Taylor, Avigail; Steinberg, Julia; Webber, Caleb Journal: American journal of medical genetics Issue: Volume 168:Issue 2(2015) Page Start: 97 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Epistasis in Neuropsychiatric Disorders. Issue 4 (April 2017) Authors: Webber, Caleb Journal: Trends in genetics Issue: Volume 33:Issue 4(2017) Page Start: 256 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genome‐Wide Association Study of Pain in Parkinson's Disease Implicates TRPM8 as a Risk Factor. Issue 4 (20th February 2020) Authors: Williams, Nigel M.; Hubbard, Leon; Sandor, Cynthia; Webber, Caleb; Hendry, Hannah; Lawton, Michael; Carroll, Camille; Chaudhuri, K. Ray; Morris, Huw; Hu, Michele T.; Grosset, Donald G.; Kobylecki, Christopher; Silverdale, Monty Journal: Movement disorders Issue: Volume 35:Issue 4(2020) Page Start: 705 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Human‐Specific Transcriptome of Ventral and Dorsal Midbrain Dopamine Neurons. Issue 6 (30th March 2020) Authors: Monzón‐Sandoval, Jimena; Poggiolini, Ilaria; Ilmer, Tobias; Wade‐Martins, Richard; Webber, Caleb; Parkkinen, Laura Journal: Annals of neurology Issue: Volume 87:Issue 6(2020) Page Start: 853 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The Parkinson's Disease Genome‐Wide Association Study Locus Browser. Issue 11 (31st August 2020) Authors: Grenn, Francis P.; Kim, Jonggeol J.; Makarious, Mary B.; Iwaki, Hirotaka; Illarionova, Anastasia; Brolin, Kajsa; Kluss, Jillian H.; Schumacher‐Schuh, Artur F.; Leonard, Hampton; Faghri, Faraz; Billingsley, Kimberley; Krohn, Lynne; Hall, Ashley; Diez‐Fairen, Monica; Periñán, Maria Teresa; Foo, Jia... Journal: Movement disorders Issue: Volume 35:Issue 11(2020) Page Start: 2056 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. TREM2 Alzheimer's variant R47H causes similar transcriptional dysregulation to TREM2 knockout in human IPSC‐derived macrophages: Developing topics. (7th December 2020) Authors: Roberts, Hazel Hall; Agarwal, Devika; Daniel, Elena Di; Webber, Caleb; James, William S; Mead, Emma; Davis, John B; Cowley, Sally A Journal: Alzheimer's & dementia Issue: Volume 16(2020)Supplement 3 Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗