Matthew Tedder - Clemson University | 人才画像

基本信息

浏览量：7

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 33 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Comprehensive EHMT1 Variants Analysis Broadens Genotype-Phenotype Associations and Molecular Mechanisms in Kleefstra Syndrome

Dmitrijs Rots,Arianne Bouman,Ayumi Yamada,Michael Levy,Alexander J. M. Dingemans,Bert B. A. de Vries,Martina Ruiterkamp-Versteeg,Nicole de Leeuw,Charlotte W. Ockeloen,Rolph Pfundt,Elke de Boer,Joost Kummeling,Bregje van Bon,Hans van Bokhoven,Nael Nadif Kasri,Hanka Venselaar,Marielle Alders,Jennifer Kerkhof,Haley McConkey,Alma Kuechler, Bart Elffers, Rixje van Beeck Calkoen, Susanna Hofman,Audrey Smith, Maria Irene Valenzuela,Siddharth Srivastava,Zoe Frazier,Isabelle Maystadt,Carmelo Piscopo,Giuseppe Merla,Meena Balasubramanian,Gijs W. E. Santen,Kay Metcalfe,Soo-Mi Park, Laurent Pasquier,Siddharth Banka,Dian Donnai,Daniel Weisberg,Gertrud Strobl-Wildemann,Annemieke Wagemans,Maaike Vreeburg, Diana Baralle,Nicola Foulds,Ingrid Scurr,Nicola Brunetti-Pierri,Johanna M. van Hagen,Emilia K. Bijlsma,Anna H. Hakonen,Carolina Courage,David Genevieve,Lucile Pinson, Francesca Forzano,Charu Deshpande, Maria L. Kluskens, Lindsey Welling,Astrid S. Plomp,Els K. Vanhoutte,Louisa Kalsner,Janna A. Hol,Audrey Putoux, Johanna Lazier,Pradeep Vasudevan,Elizabeth Ames, Jessica O'Shea,Damien Lederer,Julie Fleischer, Mary O'Connor, Melissa Pauly,Georgia Vasileiou,Andre Reis,Catherine Kiraly-Borri,Arjan Bouman, Chris Barnett,Marjan Nezarati, Lauren Borch,Gea Beunders, Kubra Ozcan, Stephanie Miot,Catharina M. L. Volker-Touw,Koen L. I. van Gassen,Gerarda Cappuccio,Katrien Janssens,Nofar Mor, Inna Shomer,Dan Dominissini,Matthew L. Tedder,Alison M. Muir,Bekim Sadikovic, Han G. Brunner,Lisenka E. L. M. Vissers, Yoichi Shinkai,Tjitske Kleefstra

AMERICAN JOURNAL OF HUMAN GENETICSno. 8 (2024): 1605-1625

引用3浏览0WOS引用

The Detection of a Strong Episignature for Chung–Jansen Syndrome, Partially Overlapping with Börjeson–Forssman–Lehmann and White–Kernohan Syndromes

Niels Vos,Sadegheh Haghshenas,Liselot van der Laan, Perle K. M. Russel,Kathleen Rooney,Michael A. Levy,Raissa Relator,Jennifer Kerkhof,Haley McConkey,Saskia M. Maas,Lisenka E. L. M. Vissers,Bert B. A. de Vries,Rolph Pfundt,Mariet W. Elting,Johanna M. van Hagen,Nienke E. Verbeek,Marjolijn C. J. Jongmans,Phillis Lakeman,Lynne Rumping,Danielle G. M. Bosch,Antonio Vitobello,Christel Thauvin-Robinet,Laurence Faivre,Sophie Nambot,Aurore Garde,Marjolaine Willems,David Genevieve,Gaël Nicolas,Tiffany Busa,Annick Toutain,Marion Gérard,Varoona Bizaoui,Bertrand Isidor,Giuseppe Merla,Maria Accadia,Charles E. Schwartz,Katrin Ounap,Mariëtte J. V. Hoffer,Marjan M. Nezarati,Marie-José H. van den Boogaard,Matthew L. Tedder,Curtis Rogers,Alfredo Brusco,Giovanni B. Ferrero,Marta Spodenkiewicz,Richard Sidlow,Alessandro Mussa,Slavica Trajkova,Emma McCann,Henry J. Mroczkowski,Sandra Jansen,Laura Donker-Kaat,Floor A. M. Duijkers,Kyra E. Stuurman,Marcel M. A. M. Mannens,Mariëlle Alders,Peter Henneman,Susan M. White,Bekim Sadikovic,Mieke M. van Haelst

Human Genetics（2024）

引用2浏览0WOS引用

Recurrent Carotid Paragangliomas in a Syndromic Patient with a Heterozygous Missense Variant in DNA Methyltransferase 3 Alpha

Ryan J. German,Blake Vuocolo,Liesbeth Vossaert,Lisa Saba,Robin Fletcher,Matthew L. Tedder,Bekim Sadikovic,Jennifer Kerkhof,Michael Wangler,Carlos A. Bacino

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2024)

引用0浏览0WOS引用

Diagnostic Utility of DNA Methylation Analysis in Genetically Unsolved Pediatric Epilepsies and CHD2 Episignature Refinement

Christy W. Laflamme,Cassandra Rastin,Soham Sengupta, Helen E. Pennington,Sophie J. Russ-Hall,Amy L. Schneider,Emily S. Bonkowski,Edith P. Almanza Fuerte, Talia J. Allan, Miranda Perez-Galey Zalusky,Joy Goffena,Sophia B. Gibson,Denis M. Nyaga,Nico Lieffering,Malavika Hebbar,Emily V. Walker,Daniel Darnell,Scott R. Olsen,Pandurang Kolekar,Mohamed Nadhir Djekidel,Wojciech Rosikiewicz,Haley Mcconkey,Jennifer Kerkhof,Michael A. Levy,Raissa Relator,Dorit Lev,Tally Lerman-Sagie,Kristen L. Park,Marielle Alders,Gerarda Cappuccio,Nicolas Chatron,Leigh Demain,David Genevieve,Gaetan Lesca,Tony Roscioli,Damien Sanlaville,Matthew L. Tedder,Sachin Gupta,Elizabeth A. Jones,Monika Weisz-Hubshman,Shamika Ketkar,Hongzheng Dai,Kim C. Worley,Jill A. Rosenfeld,Hsiao-Tuan Chao,Geoffrey Neale,Gemma L. Carvill,Zhaoming Wang,Samuel F. Berkovic,Lynette G. Sadleir,Danny E. Miller,Ingrid E. Scheffer,Bekim Sadikovic,Heather C. Mefford

NATURE COMMUNICATIONS（2024）

引用0浏览0WOSNATURE引用

P657: NSD2 Duplication Results in Distinct Phenotype and DNA Methylation Signature

Benjamin Hilton,Bekim Sadikovic,Alfredo Brusco,Giovanni Battista Ferrero,Barbara DuPont,Matthew Tedder,Raymond Louie,Nikhil Sahajpal,Erica Andersen,Zoe Lewis,Amanda Openshaw,Jennifer Kerkhof,Haley McConkey,Raissa Relator,Sadegheh Haghshenas,Jack Reilly,Kathleen Rooney

Genetics in Medicine Openno. 1 (2023): 100722-100722

引用0浏览0引用

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn