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Matthew T. Wheeler

Stanford Medicine

63H指数
455论文数
1.9W被引数
收录论文 135
发表时间
De Novo Variants Associated With Autosomal Recessive Conditions: Case Series and Implications for Genetic Testing and Counseling常染色体隐性条件相关的全新变异:病例系列及其对遗传检测和咨询的启示
err2026-09-01
err0
PREAI
errNiehaus, Annie D.; Bonner, Devon E.; Carter, Jennefer; Avello, Kayleigh; Jacob, Natalie; Neu, Matthew B.; Mendez, Rodrigo; Qiao, Wanqiong; Scott, Stuart A.; Levy, Rebecca J.; Mattas, Lauren; Schymick, Jennifer; Van Andel, Michael; Muntoni, Francesco; Mueller, Juliane; Sarkozy, Anna; DiTroia, Stephanie; O'Leary, Melanie; Neale, Ashana; O'Donnell-Luria, Anne; Toro, Camilo; Wolfe, Lynne A.; Martinez-Agosto, Julian A.; Montgomery, Stephen B.; Wheeler, Matthew T.; Bernstein, Jonathan A.; Tise, Christina G.
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Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes作者更正:非编码RNA基因RNU4-2中的biallelic变异导致一种具有独特白质变化的隐性神经发育综合征
err2026-05-18
err0
errOAAI
errRocio Rius; Alexander J. M. Blakes; Yuyang Chen; Joachim De Jonghe; François Lecoquierre; Ruebena Dawes; Benjamin Cogne; Hyung Chul Kim; Javeria R. Alvi; Florence Amblard; Morad Ansari; Annabelle Arlt; Christina Austin-Tse; Sarah Baer; Meena Balasubramanian; Elsa V. Balton; Giulia Barcia; Ana Beleza-Meireles; Jonathan A. Bernstein; Jasmin Beygo; Pierre Blanc; Nuria C. Bramswig; Frederik Braun; Daniel Buchzik; Daniel G. Calame; Jamie Campbell; Charles Coutton; Chloe A. Cunningham; Nitsuh Dargie; Christel Depienne; Katrina M. Dipple; Anne Dieux; Abhijit Dixit; Lauren Dreyer; Haowei Du; Salima El Chehadeh; Michael Field; Lisa J. Ewans; Vanessa Geiger; Richard A. Gibbs; Ian Glass; Olivier Grunewald; Paul Gueguen; Tobias B. Haack; Hamza Hadj Abdallah; Radu Harbuz; Ingo Helbig; Judit Horvath; Alexander Hustinx; Bertrand Isidor; Marie-Line Jacquemont; Fraser Jamie; Médéric Jeanne; Riley Kessler; Hannah Klinkhammer; G. Christoph Korenke; Urania Kotzaeridou; Peter Krawitz; Steven Laurie; Richard J. Leventer; Rebecca J. Levy; James R. Lupski; Pierre Marijon; Kaitlin E. McGinnis; Rodrigo Mendez; Olfa Messaoud; Caroline Nava; Mevyn Nizard; Anne O’Donnell-Luria; Melanie C. O’Leary; Simone Olivieri; Amitav Parida; Davut Pehlivan; Anna Jenne Prentice; Jennifer E. Posey; Chloe M. Reuter; Véronique Satre; Caroline Schluth-Bolard; Thomas Smol; Tipu Sultan; John Taylor; Christel Thauvin-Robinet; Julien Thevenon; Eloise Uebergang; Sandra Ueberberg; Catherine Vincent-Delorme; Evangeline Wassmer; Emma Westwood; Matthew T. Wheeler; Elif Yilmaz Gulec; Adeline Vanderver; Arastoo Vossough; Stephan J. Sanders; Siddharth Banka; Gregory M. Findlay; Daniel G. MacArthur; Cas Simons; Nicola Whiffin
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Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder出版商更正: RNU2-2中的双等位基因变体导致最普遍的隐性神经发育障碍
err2026-04-23
err0
errOAAI
errDaniel Greene; Rodrigo Mendez; Jon Lees; Mafalda Barbosa; Alessandro Bruselles; Luigi Chiriatti; Federico Ferraro; Cecilia Mancini; Rachel Schot; Frank Sleutels; Enrico Bertini; Devon E. Bonner; Arjan Bouman; Alice S. Brooks; T homas A. Cassini; Kimberly M. Ezell; Natalia Gomez-Ospina; Tjitske Kleefstra; Michael O’Donoghue; Lynette Rives; Vandana Shashi; Rebecca C. Spillmann; Mohamed Wafik; Kathleen Freson; Tahsin Stefan Barakat; Marco Tartaglia; Jonathan A. Bernstein; Andrew D. Mumford; Matthew T. Wheeler; Ernest Turro
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Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changesRNU4-2非编码RNA基因的双等位基因变异导致一种具有独特白质变化的隐性神经发育综合征。
err2026-04-08
err0
errOAAI
errRocio Rius; Alexander J. M. Blakes; Yuyang Chen; Joachim De Jonghe; François Lecoquierre; Ruebena Dawes; Benjamin Cogne; Hyung Chul Kim; Javeria R. Alvi; Florence Amblard; Morad Ansari; Annabelle Arlt; Christina Austin-Tse; Sarah Baer; Meena Balasubramanian; Elsa V. Balton; Giulia Barcia; Ana Beleza-Meireles; Jonathan A. Bernstein; Jasmin Beygo; Pierre Blanc; Nuria C. Bramswig; Frederik Braun; Daniel Buchzik; Daniel G. Calame; Jamie Campbell; Charles Coutton; Chloe A. Cunningham; Nitsuh Dargie; Christel Depienne; Katrina M. Dipple; Anne Dieux; Abhijit Dixit; Lauren Dreyer; Haowei Du; Salima El Chehadeh; Michael Field; Lisa J. Ewans; Vanessa Geiger; Richard A. Gibbs; Ian Glass; Olivier Grunewald; Paul Gueguen; Tobias B. Haack; Hamza Hadj Abdallah; Radu Harbuz; Ingo Helbig; Judit Horvath; Alexander Hustinx; Bertrand Isidor; Marie-Line Jacquemont; Fraser Jamie; Médéric Jeanne; Riley Kessler; Hannah Klinkhammer; G. Christoph Korenke; Urania Kotzaeridou; Peter Krawitz; Steven Laurie; Richard J. Leventer; Rebecca J. Levy; James R. Lupski; Pierre Marijon; Kaitlin E. McGinnis; Rodrigo Mendez; Olfa Messaoud; Caroline Nava; Mevyn Nizard; Anne O’Donnell-Luria; Melanie C. O’Leary; Simone Olivieri; Amitav Parida; Davut Pehlivan; Anna Jenne Prentice; Jennifer E. Posey; Chloe M. Reuter; Véronique Satre; Caroline Schluth-Bolard; Thomas Smol; Tipu Sultan; John Taylor; Christel Thauvin-Robinetvin; Julien Thevenon; Eloise Uebergang; Sandra Ueberberg; Catherine Vincent-Delorme; Evangeline Wassmer; Emma Westwood; Matthew T. Wheeler; Elif Yilmaz Gulec; Adeline Vanderver; Arastoo Vossough; Stephan J. Sanders; Siddharth Banka; Gregory M. Findlay; Daniel G. MacArthur; Cas Simons; Nicola Whiffin
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Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorderRNU2-2中的双等位基因变体导致最普遍的隐性神经发育障碍
err2026-03-30
err0
errOAAI
errDaniel Greene; Rodrigo Mendez; Jon Lees; Mafalda Barbosa; Alessandro Bruselles; Luigi Chiriatti; Federico Ferraro; Cecilia Mancini; Rachel Schot; Frank Sleutels; Enrico Bertini; Devon E. Bonner; Arjan Bouman; Alice S. Brooks; Thomas A. Cassini; Kimberly M. Ezell; Natalia Gomez-Ospina; Tjitske Kleefstra; Michael O’Donoghue; Lynette Rives; Vandana Shashi; Rebecca C. Spillmann; Mohamed Wafik; Kathleen Freson; Tahsin Stefan Barakat; Marco Tartaglia; Jonathan A. Bernstein; Andrew D. Mumford; Matthew T. Wheeler; Ernest Turro
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Consensus guidelines for antibacterial prophylaxis in patients with neutropenia中性粒细胞减少症患者抗菌预防的共识指南
err2025-12-01
err3
PREAI
errLindsay, Julian; Yeoh, Daniel; Teh, Benjamin W.; Reynolds, Gemma K.; Henden, Andrea; McQuilten, Zoe; Wheeler, Matthew; Hamilton, Anne; Nelson, Adam; Nakagaki, Midori; Sandhu, Shahneen; Slavin, Monica A.
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Consensus guidelines for patient and carer education on neutropenic fever中性粒细胞减少性发热患者及照护者教育共识指南
err2025-12-01
err1
PREAI
errJessop, Sophie; Harding, Emily; Beaumont, Sophie; Hickman, Joanne; Joyce, Trish; Chee, Lynette; Fernando, Shevon; Vasilunas, Nan; Luen, Stephen; Boan, Peter; Westthorp, Sheree; James, Karlie; Wheeler, Matthew; Casey, Andrea; Smibert, Olivia C.
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“Nobody listened to us for years”: Parents' experiences of provider communication in the diagnostic odyssey“多年来没有人听我们的话”:父母在诊断漫漫长路上对提供者沟通的体验
err2025-11-03
err0
PREAI
errMichelle M. Nguyen; Sevil Mahfoozi; Devon Bonner; Daphne O. Martschenko; Alisha Giri; Charis Tang; Jonathan A. Bernstein; Matthew T. Wheeler; Meghan C. Halley
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Transcriptome-wide outlier approach identifies individuals with minor spliceopathies转录组范围离群值方法识别具有微小剪接病变的个体
err2025-09-19
err0
errOAAI
errTaylor M. Arriaga; Rodrigo Mendez; Rachel A. Ungar; Devon E. Bonner; Dena R. Matalon; Gabrielle Lemire; Pagé C. Goddard; Evin M. Padhi; Alexander M. Miller; Jonathan V. Nguyen; Jialan Ma; Kevin S. Smith; Stuart A. Scott; Linda Liao; Zena Ng; Shruti Marwaha; Guney Bademci; Stephanie A. Bivona; Mustafa Tekin; Jonathan A. Bernstein; Stephen B. Montgomery; Anne O’Donnell-Luria; Matthew T. Wheeler; Vijay S. Ganesh
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Cardiac CT fractal analysis of LV noncompaction and common cardiomyopathies左心室非-compaction与常见心肌病的心脏CT分形分析
err2025-08-21
err0
PREAI
errAshish Manohar; Ashley Wong; Edgard Castillo; Allison Gunderson; Gabriel Mistelbauer; Shadi Peighambari Bagherzadeh; Francois Haddad; Kadir Caliskan; Ricardo P.J. Budde; Alexander Hirsch; Seung-Pyo Lee; Whal Lee; Anjali Owens; Harold Litt; Matthew Wheeler; Deborah H. Kwon; W.H. Wilson Tang; Koen Nieman
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Identification of candidate cardiomyopathy modifier genes through genome sequencing and RNA profiling通过基因组测序和RNA谱分析鉴定候选心肌病修饰基因
err2025-08-10
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errOAAI
errMalene E. Lindholm; Sarah Abramowitz; Daryl M. Waggott; Megan E. Grove; Frederick E. Dewey; Cuiping Pan; Aleksandra Pavlovic; Ching Shang; Yong Huang; Leore Bensabath; Rachel L. Goldfeder; Pablo Cordero; Ayca Erbilgin; James R. Priest; Hassan Chaib; Megan J. Puckelwartz; Sharlene M. Day; Elizabeth M. McNally; Thomas Cappola; Gerald W. Dorn; Euan A. Ashley; Matthew T. Wheeler
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Single Ascending-Dose Study of Selective ErbB4 Agonist JK07 in Heart Failure With Reduced Ejection Fraction选择性ErbB4激动剂JK07的单次递增剂量研究,用于射血分数降低的心力衰竭
err2025-07-29
err0
PREAI
errW.H. Wilson Tang; Johannes Steiner; Mahwash Kassi; Matthew T. Wheeler; Aferdita Spahillari; Nancy K. Sweitzer; Justin L. Grodin; Neal Solomon; Shalabh Singhal; Amanda M.G. McEwen; Samuel L. Murphy
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Valsartan and Cardiac Remodeling in Early-Stage Hypertrophic Cardiomyopathy The VANISH Randomized Clinical Trial Cardiac Magnetic Resonance SubstudyValsartan及早期肥厚型心肌病中的心脏重塑——VANISH随机临床试验的心脏磁共振亚研究
err2025-06-01
err0
PREAI
errOstrominski, John W.; Claggett, Brian L.; Jerosch-Herold, Michael; Raja, Anna Axelsson; Day, Sharlene M.; Russell, Mark W.; Zahka, Kenneth; Pereira, Alexandre C.; Colan, Steven D.; Murphy, Anne M.; Canter, Charles; Bach, Richard G.; Wheeler, Matthew T.; Rossano, Joseph W.; Owens, Anjali T.; Mestroni, Luisa; Taylor, Matthew R. G.; Patel, Amit R.; Wilmot, Ivan; Soslow, Jonathan H.; Becker, Jason R.; Lakdawala, Neal K.; Bundgaard, Henning; Vargas, Jose D.
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Proposed enhanced recommendations for interpretation of electrocardiographic screening of athletes对运动员心电图筛查结果解读的改进建议
err2025-03-11
err0
PREAI
errVictor Froelicher; Mustafa Husaini; Jason V. Tso; Samuel Montalvo; Jeffrey Christle; Marco V. Perez; David Hadley; Matthew Wheeler; Ricardo Stein; Victoria Vetter; Jeffrey J. Hsu; Irfan M. Asif; Kristofer Hedman; Anna Carlén; Kegan Moneghetti; Euan Ashley
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Researcher views on returning results from multi-omics data to research participants: insights from The Molecular Transducers of Physical Activity Consortium (MoTrPAC) Study
err2025-02-07
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errOAAI
errOrmond, Kelly E.; Stanclift, Caroline; Reuter, Chloe M.; Carter, Jennefer N.; Murphy, Kathleen E.; Lindholm, Malene E.; Wheeler, Matthew T.
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Sequentially Constrained Randomization in Preclinical Animal Studies序贯约束随机化在非临床动物研究中的应用
err2025-01-01
err0
errOAAI
errRigdon, Joseph; Walkup, Michael; Amar, David; Wheeler, Matthew T.; Goodyear, Laurie J.; Bodine, Sue; Esser, Karyn; Esserman, Denise; Miller, Michael E.
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Unlocking insights: Clinical associations from the largest 6-minute walk test collection via the my Heart Counts Cardiovascular Health Study, a fully digital smartphone platform解锁见解:通过 my Heart Counts Cardiovascular Health Study(一项完全数字化的智能手机平台),从最大规模的6分钟步行试验数据集中获取临床关联性研究
err2025-01-01
err0
PREAI
errDaniel Seung Kim; Narayan Schuetz; Anders Johnson; Alexander Tolas; Sriya Mantena; Jack W. O'Sullivan; Steven G. Hershman; Jonathan N. Myers; Jeffrey W. Christle; Marily Oppezzo; Eleni Linos; Fatima Rodriguez; C. Mikael Mattsson; Matthew T. Wheeler; Abby C. King; Herman A. Taylor; Euan A. Ashley
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The Impact of Genotype in Dilated and Arrhythmogenic Cardiomyopathy: Insights from the SHaRE Registry扩张型与心律失常性心肌病中的基因型影响:SHaRE注册研究的见解
err2024-11-12
err0
PREAI
errPadalia, Kishan; Slaven, Sarah; Medo, Kristen; Graw, Sharon; Claggett, Brian; Bundgaard, Henning; Helms, Adam; Heymans, Stephane; Ho, Carolyn; Khan, Sadiya; Lakdawala, Neal; Olivotto, Iacopo; Owens, Anjali; Prasad, Sanjay; Axelsson, Anna; Reza, Nosheen; Shore, Supriya; Sinagra, Gianfranco; Tayal, Upasana; Verdonschot, Job; Wheeler, Matthew; Taylor, Matthew; Merlo, Marco; Fornaro, Alessandra; Parikh, Victoria; Wilsbacher, Lisa; Mestroni, Luisa
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Real-world Long-term Effectiveness of Mavacamten in Patients with Symptomatic Obstructive Hypertrophic Cardiomyopathy: a Multicenter Observational Study (MARVEL-HCM)Mavacamten在症状性梗阻性肥厚型心肌病患者中的真实世界长期有效性:一项多中心观察性研究(MARVEL-HCM)
err2024-11-12
err0
PREAI
errAbraham, Theodore; Alsidawi, Said; Martinez, Matthew; Wheeler, Matthew; Roehl, Kaitlin; Patel, Ruchi; Soutar, Marybeth; Herry, Morgane; Wang, Manchen Annie; Kim, Mi-Ok; Schuler, Patricia; Dubey, Anand
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