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Barry A Chioza (Barry Chioza)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2015-2022
Publications (10 Years): 11

Top Venues

PLoS genetics

European journal of human genetics : EJHG

Genome research

Proceedings of the National Academy of Sciences of the United States of America

University of Exeter Medical School

Institute of Psychiatry at the Maudsley (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Exeter Medical School Jun 10o 2013

United Kingdom

Postdoctoral Research Fellow :: RILD Wellcome Wolfson Centre

Education History

Institute of Psychiatry at the Maudsley

United Kingdom

PHD :: Psychological Medicine

Publications

Gemma Shireby, Emma L Dempster, Stefania Policicchio, Rebecca G Smith, Ehsan Pishva, Barry A Chioza, Jonathan P Davies, Joe Burrage, Katie Lunnon, Dorothea Seiler Vellame, Seth Love, Alan Thomas, Keeley J Brookes, Kevin Morgan, Paul T Francis, Eilis J Hannon, Jonathan S Mill
DNA methylation signatures of Alzheimer's disease neuropathology in the cortex are primarily driven by variation in non-neuronal cell-types. Nature communications 13 (1) (2022)
Güney Bademci, María Lachgar, Mangesh Deokar, Mohammad Faraz Zafeer, Clemer Abad, Muzeyyen Yildirim Baylan, Neil J Ingham, Jing Chen, Claire J Sineni, Nirmal Vadgama, Ioannis Karakikes, Shengru Guo, Duygu Duman, Nitu Singh, Gaurav V Harlalka, Shirish P Jain, Barry A Chioza, Katherina Walz, Karen P Steel, Jamal Nasir, Mustafa Tekin
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice. Proceedings of the National Academy of Sciences of the United States of America 119 (26) (2022)
Zineb Ammous, Lettie E Rawlins, Hannah Jones, Joseph S Leslie, Olivia Wenger, Ethan M Scott, Jim Deline, Tom Herr, Rebecca Evans, Angela Scheid, Joanna Kennedy, Barry A Chioza, Ryan M Ames, Harold E Cross, Erik G Puffenberger, Lorna W Harries, Andrew H Crosby, Andrew H Crosby
A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorder. PLoS genetics 17 (9) (2021)
Kamal Khan, Sarmad Mehmood, Chunyu Liu, Maimoona Siddiqui, Arsalan Ahmad, Belqees Yawar Faiz, Barry A Chioza, Emma A Baple, Muhammad I Ullah, Zaineb Akram, Humayoon S Satti, Raees Khan, Gaurav V Harlalka, Muhammad Jameel, Talia Akram, Shahid M Baig, Andrew H Crosby, Muhammad J Hassan, Feng Zhang, Erica E Davis, Tahir N Khan
A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb-girdle muscular dystrophy-1 in three Pakistani pedigrees. American journal of medical genetics. Part A (2021)
Joseph S Leslie, Lettie E Rawlins, Barry A Chioza, Oluwaseun R Olubodun, Claire G Salter, James Fasham, Hannah F Jones, Harold E Cross, Simon Lam, Gaurav V Harlalka, Martina M A Muggenthaler, Andrew H Crosby, Andrew H Crosby
MNS1 variant associated with situs inversus and male infertility. European journal of human genetics : EJHG 28 (1) (2019)
Aaron R Jeffries, Reza Maroofian, Claire G Salter, Barry A Chioza, Harold E Cross, Michael A Patton, Emma L Dempster, I Karen Temple, Deborah J G Mackay, Faisal I Rezwan, Lise Aksglaede, Diana Baralle, Tabib Dabir, Matthew F Hunter, Arveen Kamath, Ajith Kumar, Ruth Newbury-Ecob, Angelo Selicorni, Amanda Springer, Lionel Van Maldergem, Vinod Varghese, Naomi Yachelevich, Katrina Tatton-Brown, Jonathan Mill, Andrew H Crosby, Andrew H Crosby
Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic aging. Genome research 29 (7) (2019)
Lettie E Rawlins, Hannah Jones, Olivia Wenger, Myat Aye, James Fasham, Gaurav V Harlalka, Barry A Chioza, Alexander Miron, Sian Ellard, Matthew N Wakeling, Andrew H Crosby, Andrew H Crosby
An Amish founder variant consolidates disruption of CEP55 as a cause of hydranencephaly and renal dysplasia. European journal of human genetics : EJHG 27 (4) (2019)
Lin Li, Xiaodong Jiao, Ilaria D'Atri, Fumihito Ono, Ralph F Nelson, Chi-Chao Chan, Naoki Nakaya, Zhiwei Ma, Yan Ma, Xiaoying Cai, Longhua Zhang, Siying Lin, Abdul Hameed, Barry A Chioza, Holly Hardy, Gavin Arno, Sarah Hull, Muhammad Imran Khan, James Fasham, Gaurav V Harlalka, Michel Michaelides, Anthony T Moore, Zeynep Hande Coban Akdemir, Shalini Jhangiani, James R Lupski, Frans P M Cremers, Raheel Qamar, Ahmed Salman, John Chilton, Jay E Self, Radha Ayyagari, Firoz Kabir, Muhammad Asif Naeem, Muhammad Ali, Javed Akram, Paul A Sieving, Sheikh Riazuddin, Emma L Baple, S Amer Riazuddin, Andrew H Crosby, J Fielding Hejtmancik
Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa. PLoS genetics 14 (8) (2018)
Muhammad Ikram Ullah, Abdul Nasir, Arsalan Ahmad, Gaurav Vijay Harlalka, Wasim Ahmad, Muhammad Jawad Hassan, Emma L Baple, Andrew H Crosby, Barry A Chioza
Identification of novel L2HGDH mutation in a large consanguineous Pakistani family- a case report. BMC medical genetics 19 (1) (2018)
Martina M A Muggenthaler, Biswajit Chowdhury, S Naimul Hasan, Harold E Cross, Brian Mark, Gaurav V Harlalka, Michael A Patton, Miho Ishida, Elijah R Behr, Sanjay Sharma, Kenneth Zahka, Eissa Faqeih, Brian Blakley, Mike Jackson, Melissa Lees, Vernon Dolinsky, Leroy Cross, Philip Stanier, Claire Salter, Emma L Baple, Fowzan Sami Alkuraya, Andrew H Crosby, Barbara Triggs-Raine, Barry A Chioza
Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice. PLoS genetics 13 (1) (2017)
Vafa Alakbarzade, Abdul Hameed, Debra Q Y Quek, Barry A Chioza, Emma L Baple, Amaury Cazenave-Gassiot, Long N Nguyen, Markus R Wenk, Arshia Q Ahmad, Ajith Sreekantan-Nair, Michael N Weedon, Phil Rich, Michael A Patton, Thomas T Warner, David L Silver, Andrew H Crosby
A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome. Nature genetics 47 (7) (2015)

Barry A Chioza.css-eqlu8i{font-size:small;padding-left:4px;} (Barry Chioza)

Publication Activity (10 Years)

Top Topics

Top Venues

Barry A Chioza (Barry Chioza)