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J

Jac Charlesworth

Menzies Institute for Medical Research
H指数:31
被引数:3,250

个人简介

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教育背景

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工作经历

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荣誉奖项

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Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype

神经疾病基因中的罕见变异及其在多发性硬化症模拟和表型中的作用

Genome Medicine
IF11.2
2025-12-100
OAAI
Nicholas B. Blackburn; Bennet J. McComish; Allan Motyer; James C. Slimmer; Stephen J. Leslie; Simon A. Broadley; Vilija G. Jokubaitis; Anneke Van Der Walt; Allan G. Kermode; Jeannette Lechner-Scott; Grant P. Parnell; Marzena J. Fabis-Pedrini; Rodney J. Scott; Stacey Jackson; Vicki E. Maltby; Jac C. Charlesworth; Kathryn P. Burdon; Bruce V. Taylor; Trevor J. Kilpatrick; Justin P. Rubio
The association between disability progression, relapses, and treatment in early relapse onset MS: an observational, multi-centre, longitudinal cohort study

早期复发MS的残疾进展，复发和治疗之间的关联: 一项观察性，多中心，纵向队列研究

SCIENTIFIC REPORTS
IF3.9
2023-07-185
OAAI
Fuh-Ngwa, Valery; Charlesworth, Jac C.; Zhou, Yuan; van der Mei, Ingrid; Melton, Phillip E.; Broadley, Simon A.; Ponsonby, Anne-Louise; Simpson-Yap, Steve; Lechner-Scott, Jeannette; Taylor, Bruce V.
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus

一项多种族全基因组关联研究表明，圆锥角膜中胶原蛋白基质的完整性和细胞分化途径

COMMUNICATIONS BIOLOGY
IF5.1
2021-03-0155
OAAI
Hardcastle, Alison J.; Liskova, Petra; Bykhovskaya, Yelena; McComish, Bennet J.; Davidson, Alice E.; Inglehearn, Chris F.; Li, Xiaohui; Choquet, Helene; Habeeb, Mahmoud; Lucas, Sionne E. M.; Sahebjada, Srujana; Pontikos, Nikolas; Lopez, Karla E. Rojas; Khawaja, Anthony P.; Ali, Manir; Dudakova, Lubica; Skalicka, Pavlina; Van Dooren, Bart T. H.; Geerards, Annette J. M.; Haudum, Christoph W.; Lo Faro, Valeria; Tenen, Abi; Simcoe, Mark J.; Patasova, Karina; Yarrand, Darioush; Yin, Jie; Siddiqui, Salina; Rice, Aine; Farraj, Layal Abi; Chen, Yii-Der Ida; Rahi, Jugnoo S.; Krauss, Ronald M.; Theusch, Elisabeth; Charlesworth, Jac C.; Szczotka-Flynn, Loretta; Toomes, Carmel; Meester-Smoor, Magda A.; Richardson, Andrea J.; Mitchell, Paul A.; Taylor, Kent D.; Melles, Ronald B.; Aldave, Anthony J.; Mills, Richard A.; Cao, Ke; Chan, Elsie; Daniell, Mark D.; Wang, Jie Jin; Rotter, Jerome I.; Hewitt, Alex W.; MacGregor, Stuart; Klaver, Caroline C. W.; Ramdas, Wishal D.; Craig, Jamie E.; Iyengar, Sudha K.; O'Brart, David; Jorgenson, Eric; Baird, Paul N.; Rabinowitz, Yaron S.; Burdon, Kathryn P.; Hammond, Chris J.; Tuft, Stephen J.; Hysi, Pirro G.
Lipid-related genetic polymorphisms significantly modulate the association between lipids and disability progression in multiple sclerosis
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
IF7.5
2019-02-1916
OAAI
Zhang, Yan; Zhou, Yuan; van der Mei, Ingrid A. F.; Simpson, Steve; Ponsonby, Anne-Louise; Lucas, Robyn M.; Tettey, Prudence; Charlesworth, Jac; Kostner, Karam; Taylor, Bruce V.; Dear, Keith; Dwyer, Terry; Blizzard, Leigh; Broadley, Simon; Kilpatrick, Trevor; Lechner-Scott, David Williamsand Jeanette; Chapman, Cameron Shawand Caron; Coulthard, Alan; Pender, Michael P.; Valery, Patricia
Rediscovering the value of families for psychiatric genetics research
MOLECULAR PSYCHIATRY
IF10.1
2018-06-2840
OA
Glahn, David C.; Nimgaonkar, Vishwajit L.; Raventos, Henriette; Contreras, Javier; McIntosh, Andrew M.; Thomson, Pippa A.; Jablensky, Assen; McCarthy, Nina S.; Charlesworth, Jac C.; Blackburn, Nicholas B.; Peralta, Juan Manuel; Knowles, Emma E. M.; Mathias, Samuel R.; Ament, Seth A.; McMahon, Francis J.; Gur, Ruben C.; Bucan, Maja; Curran, Joanne E.; Almasy, Laura; Gur, Raquel E.; Blangero, John
Rare, Potentially Pathogenic Variants in ZNF469 Are Not Enriched in Keratoconus in a Large Australian Cohort of European Descent

在欧洲血统的大型澳大利亚队列中，ZNF469中罕见的，潜在的致病性变体未在圆锥角膜中富集。

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
2017-12-1214
OAAI
Lucas, Sionne E. M.; Zhou, Tiger; Blackburn, Nicholas B.; Mills, Richard A.; Ellis, Jonathan; Leo, Paul; Souzeau, Emmanuelle; Ridge, Bronwyn; Charlesworth, Jac C.; Brown, Matthew A.; Lindsay, Richard; Craig, Jamie E.; Burdon, Kathryn P.
Key challenges in bringing CRISPR-ediated somatic cell therapy into the clinic

将CRISPR编辑的体细胞疗法引入临床的关键挑战

GENOME MEDICINE
IF11.2
2017-09-2513
OAAI
Nicol, Dianne; Eckstein, Lisa; Morrison, Michael; Sherkow, Jacob S.; Otlowski, Margaret; Whitton, Tess; Bubela, Tania; Burdon, Kathryn P.; Chalmers, Don; Chan, Sarah; Charlesworth, Jac; Critchley, Christine; Crossley, Merlin; de Lacey, Sheryl; Dickinson, Joanne L.; Hewitt, Alex W.; Kamens, Joanne; Kato, Kazuto; Kleiderman, Erika; Kodama, Satoshi; Liddicoat, John; Mackey, David A.; Newson, Ainsley J.; Nielsen, Jane; Wagner, Jennifer K.; McWhirter, Rebekah E.

研究方向

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B
Bruce Taylor
H 指数:81论文数:884被引数:3.0万
J
John Blangero
H 指数:120论文数:1,182被引数:7.4万
S
Steve Simpson
H 指数:45论文数:367被引数:1.2万
K
Kathryn P. Burdon
H 指数:63论文数:339被引数:1.4万
周
周圆
H 指数:35论文数:182被引数:4,119
A
Anne‐Louise Ponsonby
H 指数:82论文数:622被引数:2.3万
I
Ingrid van der Mei
H 指数:51论文数:332被引数:1.2万
J
Joanne E. Curran
H 指数:68论文数:490被引数:2.5万
T
Thomas D. Dyer
H 指数:56论文数:266被引数:1.3万
M
Matthew P. Johnson
H 指数:35论文数:112被引数:6,803