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M

Martina C. Cornel

vrije universiteit

55H指数
489论文数
1.1W被引数
收录论文 128
发表时间
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Patient views on receiving a pharmacogenetic passport – a mixed methods study exploring experiences and use after an opportunistic offer患者对接受药代遗传护照的看法——一项探索机会性提供后的经验和使用情况混合方法研究
errEuropean Journal of Human Genetics
IF4.6
err2026-09-15
err0
errOAAI
errEva Meier; Danny Bruins; Marieke A. R. Bak; Pierre M. Bet; Mariette A. van den Hoven; Martina Cornel; Tessel Rigter
err分享
err收藏
From evidence to implementation: key priorities for pharmacogenomics-guided treatment and prevention from a European expert workshop从证据到实施：欧洲专家研讨会提出的药物基因组学指导治疗和预防的关键优先事项
errEuropean Journal of Human Genetics
IF4.6
err2026-05-28
err0
errOAAI
errLoes Lindiwe Kreeftenberg; Lidewij Henneman; Tessel Rigter; Angelica Valz Gris; Adrián LLerena; John H. McDermott; Maureen Rutten-van Mölken; Astrid Moura Vicente; Ron H. N. van Schaik; Videha Sharma; Jesse J. Swen; Martina C. Cornel; Carla G. van El
err分享
err收藏
Towards responsible genome-wide screening: normative and stakeholder considerations迈向负责任的基因组范围筛选：规范性和利益相关者考量
errEuropean Journal of Human Genetics
IF4.6
err2026-05-22
err0
errOAAI
errCorrette Ploem; Guido de Wert; Sara Soriano Longarón; Jacobien Niebuur; Imke Christiaans; Erwin Birnie; Lidewij Henneman; Tessel Rigter; Martina Cornel; Daphne Stemkens; Helger Yntema; Sanne Van der Hout; Mirjam Plantinga
err分享
err收藏
From targeted to genome-wide DNA testing in public health screening programs—an introduction to the special issue of the European Journal of Human Genetics从靶向到全基因组DNA检测在公共卫生筛查项目中的应用——欧洲人类遗传学杂志特刊的引言
errEuropean Journal of Human Genetics
IF4.6
err2026-03-03
err0
errOAAI
errMartina C. Cornel; Saskia Smits; Belinda Dawson-McClaren
err分享
err收藏
Navigating direct-to-consumer genetic testing: experiences, decisions and perspectives of Dutch users导航直接面向消费者的基因检测：荷兰用户的经历、决策和观点
errEuropean Journal of Human Genetics
IF4.6
err2026-02-04
err0
errOAAI
errDanny Bruins; Esther A. M. Bührman; Martina C. Cornel; Marc H. W. van Mil; Margreet G. E. M. Ausems; Olga C. Damman; Tessel Rigter
err分享
err收藏
Incidental genomic findings in large scale research: using the “3-I framework” to reveal policy considerations
errFrontiers in Genetics
IF2.8
err2026-01-26
err0
errOAAI
errSuzanne Maria Onstwedder; Carla Van El; Wendy Rodenburg; Adrian Thorogood; Martina Cornelia Cornel; Tessel Rigter
err分享
err收藏
A qualitative study among guideline developers revealed challenges and strategies for rare disease guideline development一项针对指南开发者的定性研究揭示了罕见病指南开发中的挑战与策略。
errJournal of Clinical Epidemiology
IF5.2
err2025-11-07
err0
errOAAI
errMirthe J. Klein Haneveld; Willemijn F.E. Irvine; Martina C. Cornel; Federico Germini; Miranda W. Langendam; Holger J. Schünemann; Johanna H. Van der Lee; Agnies M. Van Eeghen; Charlotte M.W. Gaasterland
err分享
err收藏
Potential benefits of l-serine in children with GRIN2B loss-of-function variants: Randomized n-of-1 trialsL-丝氨酸在具有GRIN2B功能丧失性变异的儿童中的潜在益处：随机n-of-1试验
errMolecular Genetics and Metabolism
IF3.5
err2025-10-30
err0
PREAI
errBibiche den Hollander; Marieke Rothuizen-Lindenschot; Hoang Lan Le; Jennifer R. Ramautar; Annelieke R. Müller; Lisa Geertjens; Frédéric M. Vaz; Agnies M. van Eeghen; Martina C. Cornel; Bart A.W. Jacobs; Hilgo Bruining; Peter M. van de Ven; Marion M. Brands; Clara D. van Karnebeek
err分享
err收藏
DNA based screening in prevention: current practise and future promise基于DNA的筛查在预防中的作用：当前实践与未来前景
errEUROPEAN JOURNAL OF PUBLIC HEALTH
IF3.9
err2025-10-01
err0
PREAI
errCornel, M.
err分享
err收藏
Overcoming treatment implementation barriers for individuals with rare diseases using single-case experimental designs使用单案例实验设计克服罕见病患者治疗实施障碍
errGenetics in Medicine
IF6.2
err2025-09-29
err0
PREAI
errAnnelieke R. Müller; Bibiche den Hollander; Agnies M. van Eeghen; Peter M. van de Ven; Martina Cornel; Mieke van Haelst; Jan J. Sprengers; Hilgo Bruining; Marion M. Brands; Clara D. van Karnebeek
err分享
err收藏
Emerging and evolving values in the changing landscape of genomics基因组学发展变化背景下新兴与演变的价值观
errFRONTIERS IN GENETICS
IF2.8
err2025-04-25
err0
errOAAI
errSiermann, Maria; Mohan, Riya; Bunnik, Eline M.; Cambon-Thomsen, Anne; Chadwick, Ruth; Cornel, Martina C.; van Delden, Johannes J. M.; Joly, Yann; Molnar-Gabor, Fruzsina; Jimenez, Maria Pilar Nicolas; Pinxten, Wim; Rial-Sebbag, Emmanuelle; Shabani, Mahsa; Van Steijvoort, Eva; Wallace, Susan E.; Zawati, Ma'n H.; Knoppers, Bartha Maria; Borry, Pascal
err分享
err收藏
'We are the engine': a focus group study on clinical practice guideline development with European patient advocates for rare congenital malformations and/or intellectual disability
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2025-04-10
err0
errOAAI
errHaneveld, Mirthe Jasmijn Klein; de Mortier, Chloe Aymee; Hugon, Anne; Cornel, Martina Cornelia; Gaasterland, Charlotte Maria Wilhelmina; van Eeghen, Agnies Marguerite
err分享
err收藏
SIMPATHIC: Accelerating drug repurposing for rare diseases by exploiting SIMilarities in clinical and molecular PATHologySIMPATHIC: 通过利用临床和分子病理学的相似性来加速罕见疾病的药物再利用
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2025-03-01
err0
PREAI
errvan Karnebeek, Clara D. M.; Muller, Annelieke R.; Benkemoun, Laura; Boussaad, Ibrahim; Cornel, Martina C.; Inthout, Joanna; de Kort, Martin; Martins, Sofia de Oliveira; Prigione, Alessandro; Rigter, Tessel; Roes, Kit C. B.; Sanchez, Anna; Schipper, Raymond; Wilkinson, Mark D.; 't Hoen, Peter A. C.
err分享
err收藏
A decade of public engagement regarding human germline gene editing: a systematic scoping review
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2024-11-28
err1
errOAAI
errGeuverink, Wendy P.; Houtman, Diewertje; Retel Helmrich, Isabel R. A.; Kist, Joosje D.; Henneman, Lidewij; Cornel, Martina C.; Riedijk, Sam R.
err分享
err收藏
Do we care? Reporting of genetic diagnoses in multidisciplinary intellectual disability care: a retrospective chart review我们在乎吗？多学科智力残疾护理中遗传诊断的报告: 回顾性图表回顾
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2024-09-16
err0
errOAAI
errMuller, Annelieke R.; Boot, Erik; Notermans, Stijn B.; Schuengel, Carlo; Henneman, Lidewij; Cornel, Martina C.; van Haelst, Mieke M.; Alders, Marielle; van Karnebeek, Clara D. M.; Bijl, Bas; Wijburg, Frits A.; van Eeghen, Agnies M.
err分享
err收藏
Engagement of patients and the public in personalised prevention in Europe using genomic information: a scoping review
errFRONTIERS IN PUBLIC HEALTH
IF3.4
err2024-09-12
err0
errOAAI
errKreeftenberg, Loes Lindiwe; Henneman, Lidewij; Ket, Johannes C. F.; Cornel, Martina C.; van El, Carla G.
err分享
err收藏
The impact of counselors' values and religious beliefs on their role identity and perspectives on heritable genome editing: a qualitative interview study
errHUMANITIES & SOCIAL SCIENCES COMMUNICATIONS
IF3.6
err2024-08-22
err0
errOAAI
errGeuverink, Wendy P.; Gitsels, Janneke T.; Cornel, Martina C.; Peerbolte, Bert Jan Lietaert; Prinds, Christina; van El, Carla G.; Martin, Linda
err分享
err收藏
Policy Guidance for Direct-to-Consumer Genetic Testing Services:Framework Development Study直接面向消费者的基因检测服务的政策指导: 框架发展研究
errJOURNAL OF MEDICAL INTERNET RESEARCH
IF6
err2024-07-17
err0
PREAI
errOnstwedder, Suzanne Maria; Jansen, Marleen Elizabeth; Cornel, Martina Cornelia; Rigter, Tessel
err分享
err收藏
Perceptions of reproductive healthcare providers regarding their involvement in offering expanded carrier screening in fertility clinics: a qualitative study
errREPRODUCTIVE BIOMEDICINE ONLINE
IF3.5
err2024-07-01
err3
errOAAI
errKlein, David; van Dijke, Ivy; van Langen, Irene M.; Dondorp, Wybo; Lakeman, Phillis; Henneman, Lidewij; Cornel, Martina C.
err分享
err收藏
Improving care for rare genetic neurodevelopmental disorders: A systematic review and critical appraisal of clinical practice guidelines using AGREE II
errGENETICS IN MEDICINE
IF6.2
err2024-04-01
err1
errOAAI
errHaneveld, Mirthe J. Klein; Hieltjes, Imeze J.; Langendam, Miranda W.; Cornel, Martina C.; Gaasterland, Charlotte M. W.; Van Eeghen, Agnies M.
err分享
err收藏

研究方向

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合作学者
合作期刊
C
Cornelia M. van Duijn
H 指数: 238 · 论文数: 1.9K
H
Holger J. Schünemann
H 指数: 174 · 论文数: 1.2K
P
Paolo Boffetta
H 指数: 167 · 论文数: 2.1K
S
Stefan M. Pfister
H 指数: 159 · 论文数: 2.1K
M
Michael J. Ackerman
H 指数: 154 · 论文数: 1.4K
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