Andrea Seeley - Department of Pediatrics, Geisinger Medical Center

基本信息

浏览量：0

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 19 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

Trichorhinophalangeal Syndrome Orthopaedic Manifestations and Management: A Systematic Review

Emily Ellison, Steven J Grampp, Seth Ellison,Andrea Seeley,Mark Seeley

Journal of the American Academy of Orthopaedic Surgeons Global research & reviewsno. 8 (2024)

引用0浏览0WOS引用

PSMC3 Proteasome Subunit Variants Are Associated with Neurodevelopmental Delay and Type I Interferon Production

Frederic Ebstein,Sebastien Kuery,Victoria Most,Cory Rosenfelt,Marie-Pier Scott-Boyer,Geeske M. van Woerden,Thomas Besrard,Jonas Johannes Papendorf,Maja Studencka-Turski,Tianyun Wang,Tzung-Chien Hsieh,Richard Golnik,Dustin Baldridge,Cara Forster,Charlotte de Konink,Selina M. W. Teurlings,Virginie Vignard,Richard H. van Jaarsveld,Lesley Ades,Benjamin Cogne,Cyril Mignot,Wallid Deb,Marjolijn C. J. Jongmans,F. Sessions Cole,Marie-Jose H. van den Boogaard,Jennifer A. Wambach,Daniel J. Wegner,Sandra Yang,Vickie Hannig,Jennifer Ann Brault,Neda Zadeh,Bruce Bennetts,Boris Keren,Anne-Claire Gelineau,Zoee Powis,Meghan Towne,Kristine Bachman,Andrea Seeley,Anita E. Beck,Jennifer Morrison,Rachel Westman,Kelly Averill,Theresa Brunet,Judith Haasters,Melissa T. Carter,Matthew Osmond,Patricia G. Wheeler,Francesca Forzano,Shehla Mohammed,Yannis Trakadis,Andrea Accogli,Rachel Harrison,Yiran Guo,Hakon Hakonarson,Sophie Rondeau,Genevieve Baujat,Giulia Barcia,Rene Guenther Feichtinger,Johannes Adalbert Mayr,Martin Preisel,Frederic Laumonnier,Tilmann Kallinich,Alexej Knaus,Bertrand Isidor,Peter Krawitz,Uwe Voelker,Elke Hammer,Arnaud Droit,Evan E. Eichler,Ype Elgersma,Peter W. Hildebrand,Francois Bolduc,Elke Krueger,Stephane Bezieau

Science translational medicine（2023）

引用5浏览0WOSSCIENCE引用

Orthopaedic Management of Loeys-Dietz Syndrome: A Systematic Review

Conor P Lynch, Mira Patel,Andrea H Seeley,Mark A Seeley

Journal of the American Academy of Orthopaedic Surgeons Global research & reviews（2021）

引用3浏览0WOS引用

De novo variants in the PSMC3 proteasome AAA-ATPase subunit gene cause neurodevelopmental disorders associated with type I interferonopathies

Frédéric Ebstein,Sébastien Küry,Victoria Most,Cory Rosenfelt,Marie-Pier Scott- Boyer,Geeske M. van Woerden,Thomas Besnard,Jonas Johannes Papendorf,Maja Studencka-Turski,Tianyun Wang,Tzung-Chien Hsieh,Richard Golnik,Dustin Baldridge,Cara Forster,Charlotte de Konink,Selina M.W. Teurlings,Virginie Vignard,Richard H. van Jaarsveld,Lesley Ades,Benjamin Cogné,Cyril Mignot,Wallid Deb,Marjolijn C.J. Jongmans,F. Sessions Cole,Marie-José H. van den Boogaard,Jennifer A. Wambach,Daniel J. Wegner,Sandra Yang,Vickie Hannig,Jennifer Ann Brault,Neda Zadeh,Bruce Bennetts,Boris Keren,Anne-Claire Gélineau,Zöe Powis,Meghan Towne,Kristine Bachman,Andrea Seeley,Anita E. Beck,Jennifer Morrison,Rachel Westman,Kelly Averill,Theresa Brunet,Judith Haasters,Melissa T. Carter,Matthew Osmond,Patricia G. Wheeler,Francesca Forzano,Shehla Mohammed,Yannis Trakadis,Andrea Accogli,Rachel Harrison,Deciphering Developmental Disorders Study, CareRare Canada Consortium,Sophie Rondeau,Geneviève Baujat,Giulia Barcia,René Günther Feichtinger,Johannes Adalbert Mayr,Martin Preisel,Frédéric Laumonnier,Alexej Knaus,Bertrand Isidor,Peter Krawitz,Uwe Völker,Elke Hammer,Arnaud Droit,Evan E. Eichler,Ype Elgersma,Peter W. Hildebrand,François Bolduc,Elke Krüger,Stéphane Bézieau

medRxiv (Cold Spring Harbor Laboratory) (2021)

引用1浏览0引用

CSNK2B: A Broad Spectrum of Neurodevelopmental Disability and Epilepsy Severity

Michelle E. Ernst,Evan H. Baugh,Amanda Thomas,Louise Bier,Natalie Lippa,Nicholas Stong,Maureen S. Mulhern,Sulagna Kushary,Cigdem I. Akman,Erin L. Heinzen,Raymond Yeh,Weimin Bi,Neil A. Hanchard,Lindsay C. Burrage,Magalie S. Leduc,Josephine S. C. Chong,Renee Bend,Michael J. Lyons,Jennifer A. Lee,Pim Suwannarat,Eva Brilstra,Marleen Simon,Marije Koopmans,Ellen van Binsbergen,Daniel Groepper,Julie Fleischer,Caroline Nava,Boris Keren,Cyril Mignot,Sophie Mathieu,Grazia M. S. Mancini,Suneeta Madan-Khetarpal,Elena M. Infante,Judith Bluvstein,Andrea Seeley,Kristine Bachman,Eric W. Klee,Laura E. Schultz-Rogers,Linda Hasadsri,Sarah Barnett,Marissa S. Ellingson,Matthew J. Ferber,Vinodh Narayanan, Keri Ramsey,Anita Rauch,Pascal Joset,Katharina Steindl,Theodore Sheehan,Annapurna Poduri,Alejandra Vasquez,Claudia Ruivenkamp,Susan M. White,Lynn Pais,Kristin G. Monaghan,David B. Goldstein,Tristan T. Sands,Vimla Aggarwal

Epilepsia（2021）

引用12浏览0WOS引用

GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder

Christine Shieh,Natasha Jones,Brigitte Vanle,Margaret Au,Alden Y. Huang,Ana P. G. Silva,Hane Lee,Emilie D. Douine,Maria G. Otero, Andrew Choi,Katheryn Grand,Ingrid P. Taff,Mauricio R. Delgado,M. J. Hajianpour,Andrea Seeley,Luis Rohena,Hilary Vernon,Karen W. Gripp,Samantha A. Vergano,Sonal Mahida,Sakkubai Naidu,Ana Berta Sousa,Karen E. Wain,Thomas D. Challman,Geoffrey Beek,Donald Basel,Judith Ranells,Rosemarie Smith,Roman Yusupov,Mary-Louise Freckmann,Lisa Ohden,Laura Davis-Keppen,David Chitayat,James J. Dowling,Richard Finkel,Andrew Dauber,Rebecca Spillmann,Loren D. M. Pena,Kay Metcalfe,Miranda Splitt,Katherine Lachlan,Shane A. McKee,Jane Hurst,David R. Fitzpatrick,Jenny E. V. Morton,Helen Cox,Sunita Venkateswaran,Juan I. Young,Eric D. Marsh,Stanley F. Nelson,Julian A. Martinez,John M. Graham,Usha Kini,Joel P. Mackay,Tyler Mark Pierson

GENETICS IN MEDICINE (2020)

引用0浏览0引用

Pediatric Reporting of Genomic Results Study (PROGRESS): a Mixed-Methods, Longitudinal, Observational Cohort Study Protocol to Explore Disclosure of Actionable Adult- and Pediatric-Onset Genomic Variants to Minors and Their Parents

Juliann M. Savatt,Jennifer K. Wagner,Steven Joffe,Alanna Kulchak Rahm,Marc S. Williams,Angela R. Bradbury,F. Daniel Davis, Julie Hergenrather,Yirui Hu,Melissa A. Kelly,H. Lester Kirchner, Michelle N. Meyer,Jessica Mozersky,Sean M. O'Dell, Josie Pervola,Andrea Seeley,Amy C. Sturm,Adam H. Buchanan

BMC pediatricsno. 1 (2020)

引用10浏览0WOS引用

Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder

Christine Shieh,Natasha Jones,Brigitte Vanle,Margaret Au,Alden Y Huang,Ana P G Silva,Hane Lee,Emilie D Douine,Maria G Otero,Andrew Choi,Katheryn Grand,Ingrid P Taff,Mauricio R Delgado,M J Hajianpour,Andrea Seeley,Luis Rohena,Hilary Vernon,Karen W Gripp,Samantha A Vergano,Sonal Mahida,Sakkubai Naidu,Ana Berta Sousa,Karen E Wain,Thomas D Challman,Geoffrey Beek,Donald Basel,Judith Ranells,Rosemarie Smith,Roman Yusupov,Mary-Louise Freckmann,Lisa Ohden,Laura Davis-Keppen,David Chitayat,James J Dowling,Richard Finkel,Andrew Dauber,Rebecca Spillmann,Loren D M Pena,Undiagnosed Diseases Network,Kay Metcalfe,Miranda Splitt,Katherine Lachlan,Shane A McKee,Jane Hurst,David R Fitzpatrick,Jenny E V Morton,Helen Cox,Sunita Venkateswaran,Juan I Young,Eric D Marsh,Stanley F Nelson,Julian A Martinez,John M Graham,Usha Kini,Joel P Mackay,Tyler Mark Pierson

Genetics in medicine : official journal of the American College of Medical Geneticsno. 4 (2020): 822-822

引用11浏览0WOS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