Browse by People


Up a level
Export as [feed] RSS [feed] RSS 2.0 Short Author List
Number of items: 4.


Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H, Nowak, Catherine B, Douglas, Jessica, Swoboda, Kathryn J
et al (show 368 more authors) (2019) CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018). NATURE COMMUNICATIONS, 10 (1). 883-.


Billingsley, Kimberley, Barbosa, Ines, Bandrés-Ciga, Sara, Quinn, John ORCID: 0000-0003-3551-7803, Bubb, Vivien, Deshpande, Charu, Botia, Juan, Reynolds, Regina, Zhang, David, Simpson, Michael ORCID: 0000-0002-8539-8753
et al (show 8 more authors) (2018) Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk. BioRxiv.


Billingsley, Kimberley J, Barbosa, Ines A, Bandres-Ciga, Sara, Quinn, John P ORCID: 0000-0003-3551-7803, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Deshpande, Charu, Botia, Juan A, Reynolds, Regina H, Zhang, David, Simpson, Michael A
et al (show 136 more authors) (2019) Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset. NPJ PARKINSONS DISEASE, 5 (1). 8-.


Farmery, James HR, Smith, Mike L, Lynch, Andy G, Huissoon, Aarnoud, Furnell, Abigail, Mead, Adam, Levine, Adam P, Manzur, Adnan, Thrasher, Adrian, Greenhalgh, Alan
et al (show 341 more authors) (2018) Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (vol 8, 1300, 2018). SCIENTIFIC REPORTS, 8 (1). 13376-.

This list was generated on Sat Mar 2 13:31:38 2024 GMT.