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

Empowering Parents of Adolescents at Elevated Risk of Suicide: Co-Designing an Adaptation to a Coach-Assisted, Digital Parenting Intervention

赋能有自杀高风险青少年的父母:共同设计一种适应教练辅助的数字化育儿干预方案

Cao, Alice; Wu, Ling; Melvin, Glenn; Cardamone-Breen, Mairead; Broomfield, Grace; Seguin, Joshua; Salvaris, Chloe; Xie, Jue; Basur, Dhruv; Bartindale, Tom; McNaney, Roisin; Olivier, Patrick; Yap, Marie Bee Hui

Designing a Cross-Cultural Bridging Intervention to Increase Under-Served Immigrant Parents' Engagement in Evidence-Based Online Parenting Programs: A Co-Design Study with Indian-Origin Parents in Australia

设计一项跨文化桥梁干预措施,以提高服务不足的移民父母参与循证在线育儿项目的积极性:一项与澳大利亚印度裔父母共同设计的研究

Bapuji, Sunita Bayyavarapu; Wu, Ling; Seguin, Joshua; Olivier, Patrick; Yap, Marie Bee Hui

Embedding Technology-Assisted Parenting Interventions in Real-World Settings to Empower Parents of Children With Adverse Childhood Experiences: Co-Design Study

将技术辅助育儿干预措施融入真实情境,以增强经历过童年逆境儿童的父母的能力:共同设计研究

Aldridge, Grace; Wu, Ling; Seguin, Joshua Paolo; Robinson, Jennifer; Battaglia, Elizabeth; Olivier, Patrick; Yap, Marie B H

Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies

DOT1L 中罕见的新生获得功能错义变异与发育迟缓和先天性异常有关

Zelha Nil, Ashish R Deshwar, Yan Huang, Scott Barish, Xi Zhang, Sanaa Choufani, Polona Le Quesne Stabej, Ian Hayes, Patrick Yap, Chad Haldeman-Englert, Carolyn Wilson, Trine Prescott, Kristian Tveten, Arve Vøllo, Devon Haynes, Patricia G Wheeler, Jessica Zon, Cheryl Cytrynbaum, Rebekah Jobling, Moir

De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder

TLK2基因的新生突变和遗传性功能丧失变异:一种独特神经发育障碍的临床和基因型-表型评估

Reijnders, Margot R F; Miller, Kerry A; Alvi, Mohsan; Goos, Jacqueline A C; Lees, Melissa M; de Burca, Anna; Henderson, Alex; Kraus, Alison; Mikat, Barbara; de Vries, Bert B A; Isidor, Bertrand; Kerr, Bronwyn; Marcelis, Carlo; Schluth-Bolard, Caroline; Deshpande, Charu; Ruivenkamp, Claudia A L; Wieczorek, Dagmar; Baralle, Diana; Blair, Edward M; Engels, Hartmut; Lüdecke, Hermann-Josef; Eason, Jacqueline; Santen, Gijs W E; Clayton-Smith, Jill; Chandler, Kate; Tatton-Brown, Katrina; Payne, Katelyn; Helbig, Katherine; Radtke, Kelly; Nugent, Kimberly M; Cremer, Kirsten; Strom, Tim M; Bird, Lynne M; Sinnema, Margje; Bitner-Glindzicz, Maria; van Dooren, Marieke F; Alders, Marielle; Koopmans, Marije; Brick, Lauren; Kozenko, Mariya; Harline, Megan L; Klaassens, Merel; Steinraths, Michelle; Cooper, Nicola S; Edery, Patrick; Yap, Patrick; Terhal, Paulien A; van der Spek, Peter J; Lakeman, Phillis; Taylor, Rachel L; Littlejohn, Rebecca O; Pfundt, Rolph; Mercimek-Andrews, Saadet; Stegmann, Alexander P A; Kant, Sarina G; McLean, Scott; Joss, Shelagh; Swagemakers, Sigrid M A; Douzgou, Sofia; Wall, Steven A; Küry, Sébastien; Calpena, Eduardo; Koelling, Nils; McGowan, Simon J; Twigg, Stephen R F; Mathijssen, Irene M J; Nellaker, Christoffer; Brunner, Han G; Wilkie, Andrew O M

Recurrent loss of heterozygosity correlates with clinical outcome in pancreatic neuroendocrine cancer

复发性杂合性缺失与胰腺神经内分泌癌的临床结果相关

Ben Lawrence #, Cherie Blenkiron #, Kate Parker #, Peter Tsai, Sandra Fitzgerald, Paula Shields, Tamsin Robb, Mee Ling Yeong, Nicole Kramer, Sarah James, Mik Black, Vicky Fan, Nooriyah Poonawala, Patrick Yap, Esther Coats, Braden Woodhouse, Reena Ramsaroop, Masato Yozu, Bridget Robinson, Kimiora Hen

Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures"

纤连蛋白基因突变导致一种伴有“角状骨折”的脊椎干骺端发育不良亚型

Chae Syng Lee ,He Fu ,Nissan Baratang ,Justine Rousseau ,Heena Kumra ,V Reid Sutton ,Marcello Niceta ,Andrea Ciolfi ,Guilherme Yamamoto ,Débora Bertola ,Carlo L Marcelis ,Dorien Lugtenberg ,Andrea Bartuli ,Choel Kim ,Julie Hoover-Fong ,Nara Sobreira ,Richard Pauli ,Carlos Bacino ,Deborah Krakow ,Jillian Parboosingh ,Patrick Yap ,Ariana Kariminejad ,Marie T McDonald ,Mariana I Aracena ,Ekkehart Lausch ,Sheila Unger ,Andrea Superti-Furga ,James T Lu ,Marco Tartaglia ,Brendan H Lee ,Dieter P Reinhardt ,Philippe M Campeau