日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Perceptual interventions ameliorate statistical discrimination in learning agents

感知干预可以改善学习代理中的统计判别能力。

Duéñez-Guzmán, Edgar A; Comanescu, Ramona; Mao, Yiran; McKee, Kevin R; Coppin, Ben; Sadedin, Suzanne; Chiappa, Silvia; Vezhnevets, Alexander S; Bakker, Michiel A; Bachrach, Yoram; Isaac, William; Tuyls, Karl; Leibo, Joel Z

Scalable automated reanalysis of genomic data in research and clinical rare disease cohorts

可扩展的基因组数据自动化再分析在研究和临床罕见病队列中的应用

Welland, Matthew J; Ahlquist, K D; De Fazio, Paul; Austin-Tse, Christina; Pais, Lynn; Wedd, Laura; Bryen, Samantha; Rius, Rocio; Franklin, Michael; Morrison, Caitlin; Hall, Giles; Gauthier, Laura; Bloemendal, Alex; Francis, David I; Mallett, Andrew J; Mallawaarachchi, Amali; Lockhart, Paul J; Leventer, Richard; Scheffer, Ingrid E; Howell, Katherine B; Kassahn, Karin S; Scott, Hamish S; McGaughran, Julie; Christodoulou, John; Thorburn, David R; Thompson, Bryony A; Patel, Chirag V; Smith, Greg; O'Donnell-Luria, Anne; Sadedin, Simon; Rehm, Heidi L; Lunke, Sebastian; Wander, Jeremiah; Samocha, Kaitlin E; Simons, Cas; MacArthur, Daniel G; Stark, Zornitza

Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study

BabyScreen+ 基因组新生儿筛查研究的可行性、可接受性和临床结果

Lunke, Sebastian; Downie, Lilian; Caruana, Jade; Kugenthiran, Nathasha; De Fazio, Paul; Hollizeck, Sebastian; Bouffler, Sophie E; Amor, David J; Archibald, Alison D; Bombard, Yvonne; Christodoulou, John; Clausen, Marc; Fagan, Wendy; Gaff, Clara; Greaves, Ronda F; Gyngell, Christopher; Kanga-Parabia, Anaita; Lang, Nitzan; Lee, Crystle; Lynch, Fiona; Marty, Anthony; Marty, Melanie; McGregor, Candice; Riseley, Jessica; Sadedin, Simon; Scarff, Katrina; da Cunha Torres, Michelle; Tutty, Erin; Vang, Ching; Wall, Meaghan; Wong, Ee Ming; Yeung, Alison; Goranitis, Ilias; Best, Stephanie; Vears, Danya F; Stark, Zornitza

Benchmarking pharmacogenomics genotyping tools: Performance analysis on short-read sequencing samples and depth-dependent evaluation

药物基因组学基因分型工具的基准测试:基于短读长测序样本的性能分析和深度依赖性评估

Halman, Andreas; Lunke, Sebastian; Sadedin, Simon; Moore, Claire; Conyers, Rachel

Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns

澳大利亚新生儿智力障碍和自闭症特征的表观基因组筛查

Alshawsh, Mohammed; Wake, Melissa; Gecz, Jozef; Corbett, Mark; Saffery, Richard; Pitt, James; Greaves, Ronda; Williams, Katrina; Field, Michael; Cheong, Jeanie; Bui, Minh; Arora, Sheena; Sadedin, Simon; Lunke, Sebastian; Wall, Meg; Amor, David J; Godler, David E

Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol

前瞻性队列研究:新生儿基因组筛查:BabyScreen+试点研究方案

Lunke, Sebastian; Bouffler, Sophie E; Downie, Lilian; Caruana, Jade; Amor, David J; Archibald, Alison; Bombard, Yvonne; Christodoulou, John; Clausen, Marc; De Fazio, Paul; Greaves, Ronda F; Hollizeck, Sebastian; Kanga-Parabia, Anaita; Lang, Nitzan; Lynch, Fiona; Peters, Riccarda; Sadedin, Simon; Tutty, Erin; Eggers, Stefanie; Lee, Crystle; Wall, Meaghan; Yeung, Alison; Gaff, Clara; Gyngell, Christopher; Vears, Danya F; Best, Stephanie; Goranitis, Ilias; Stark, Zornitza

Emotions and courtship help bonded pairs cooperate, but emotional agents are vulnerable to deceit

情感和求偶行为有助于建立亲密关系的伴侣合作,但情感主体容易受到欺骗。

Sadedin, Suzanne; Duéñez-Guzmán, Edgar A; Leibo, Joel Z

Elusive variants in autosomal recessive disease: how can we improve timely diagnosis?

常染色体隐性遗传病中难以捉摸的变异:我们如何才能提高及时诊断率?

Horton, Ari E; Lunke, Sebastian; Sadedin, Simon; Fennell, Andrew P; Stark, Zornitza

Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation

Shariant平台:促进澳大利亚临床基因检测实验室间的证据共享,以支持变异解读。

Tudini, Emma; Andrews, James; Lawrence, David M; King-Smith, Sarah L; Baker, Naomi; Baxter, Leanne; Beilby, John; Bennetts, Bruce; Beshay, Victoria; Black, Michael; Boughtwood, Tiffany F; Brion, Kristian; Cheong, Pak Leng; Christie, Michael; Christodoulou, John; Chong, Belinda; Cox, Kathy; Davis, Mark R; Dejong, Lucas; Dinger, Marcel E; Doig, Kenneth D; Douglas, Evelyn; Dubowsky, Andrew; Ellul, Melissa; Fellowes, Andrew; Fisk, Katrina; Fortuno, Cristina; Friend, Kathryn; Gallagher, Renee L; Gao, Song; Hackett, Emma; Hadler, Johanna; Hipwell, Michael; Ho, Gladys; Hollway, Georgina; Hooper, Amanda J; Kassahn, Karin S; Krishnaraj, Rahul; Lau, Chiyan; Le, Huong; San Leong, Huei; Lundie, Ben; Lunke, Sebastian; Marty, Anthony; McPhillips, Mary; Nguyen, Lan T; Nones, Katia; Palmer, Kristen; Pearson, John V; Quinn, Michael C J; Rawlings, Lesley H; Sadedin, Simon; Sanchez, Louisa; Schreiber, Andreas W; Sigalas, Emanouil; Simsek, Aygul; Soubrier, Julien; Stark, Zornitza; Thompson, Bryony A; U, James; Vakulin, Cassandra G; Wells, Amanda V; Wise, Cheryl A; Woods, Rick; Ziolkowski, Andrew; Brion, Marie-Jo; Scott, Hamish S; Thorne, Natalie P; Spurdle, Amanda B

Lessons learnt from multifaceted diagnostic approaches to the first 150 families in Victoria's Undiagnosed Diseases Program

从维多利亚州未确诊疾病计划前150个家庭的多方面诊断方法中汲取的经验教训

Cloney, Thomas; Gallacher, Lyndon; Pais, Lynn S; Tan, Natalie B; Yeung, Alison; Stark, Zornitza; Brown, Natasha J; McGillivray, George; Delatycki, Martin B; de Silva, Michelle G; Downie, Lilian; Stutterd, Chloe A; Elliott, Justine; Compton, Alison G; Lovgren, Alysia; Oertel, Ralph; Francis, David; Bell, Katrina M; Sadedin, Simon; Lim, Sze Chern; Helman, Guy; Simons, Cas; Macarthur, Daniel G; Thorburn, David R; O'Donnell-Luria, Anne H; Christodoulou, John; White, Susan M; Tan, Tiong Yang