R
R. Tanner Hagelstrom
Researcher at Illumina
Publications - 5
Citations - 118
R. Tanner Hagelstrom is an academic researcher from Illumina. The author has contributed to research in topics: Randomized controlled trial & 1p36 deletion syndrome. The author has an hindex of 3, co-authored 5 publications receiving 29 citations.
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Journal ArticleDOI
Effect of Whole-Genome Sequencing on the Clinical Management of Acutely Ill Infants With Suspected Genetic Disease: A Randomized Clinical Trial
Ian D. Krantz,Livija Medne,Jamila M Weatherly,K Taylor Wild,Sawona Biswas,Sawona Biswas,Batsal Devkota,Tiffiney R. Hartman,Luca Brunelli,Luca Brunelli,Kristen P. Fishler,Omar A. Abdul-Rahman,Joshua C. Euteneuer,Denise M. Hoover,David Dimmock,David Dimmock,John P. Cleary,Lauge Farnaes,Jason Knight,Adam Schwarz,Ofelia Vargas-Shiraishi,Kristin Wigby,Kristin Wigby,Neda Zadeh,Marwan Shinawi,Jennifer A. Wambach,Dustin Baldridge,F. Sessions Cole,Daniel J. Wegner,Nora Urraca,Nora Urraca,Shannon Holtrop,Roya Mostafavi,Roya Mostafavi,Henry Joel Mroczkowski,Henry Joel Mroczkowski,Eniko K. Pivnick,Eniko K. Pivnick,Jewell C. Ward,Jewell C. Ward,Ajay J. Talati,Ajay J. Talati,Chester W. Brown,Chester W. Brown,John W Belmont,Julia L Ortega,Keisha D Robinson,W Tyler Brocklehurst,Denise L. Perry,Subramanian S. Ajay,R. Tanner Hagelstrom,Maren Bennett,Vani Rajan,Ryan J. Taft +53 more
TL;DR: In this paper, the effect of whole-genome sequencing (WGS) on clinical management in a racially and ethnically diverse and geographically distributed population of acutely ill infants in the US was investigated.
Journal ArticleDOI
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females
Francesca Clementina Radio,Kaifang Pang,Andrea Ciolfi,Michael A. Levy,Andres Hernandez-Garcia,Lucia Pedace,Francesca Pantaleoni,Zhandong Liu,Elke de Boer,Adam Jackson,Adam Jackson,Alessandro Bruselles,Haley McConkey,Emilia Stellacci,Stefania Lo Cicero,Marialetizia Motta,Rosalba Carrozzo,Maria Lisa Dentici,Kirsty McWalter,Megha Desai,Kristin G. Monaghan,Aida Telegrafi,Christophe Philippe,Antonio Vitobello,Margaret Au,Katheryn Grand,Pedro A. Sanchez-Lara,Joanne Baez,Kristin Lindstrom,Peggy Kulch,Jessica Sebastian,Suneeta Madan-Khetarpal,Chelsea Roadhouse,Jennifer MacKenzie,Berrin Monteleone,Carol J Saunders,July K. Jean Cuevas,Laura A Cross,Dihong Zhou,Taila Hartley,Sarah L. Sawyer,Fabíola Paoli Monteiro,Tania Vertemati Secches,Fernando Kok,Laura Schultz-Rogers,Erica L. Macke,Eva Morava,Eric W. Klee,Jennifer L. Kemppainen,Maria Iascone,Angelo Selicorni,Romano Tenconi,David J. Amor,Lynn Pais,Lyndon Gallacher,Peter D. Turnpenny,Karen Stals,Sian Ellard,Sara Cabet,Gaetan Lesca,Joset Pascal,Katharina Steindl,Sarit Ravid,Karin Weiss,Alison M R Castle,Melissa T. Carter,Louisa Kalsner,Bert B.A. de Vries,Bregje W.M. van Bon,Marijke R. Wevers,Rolph Pfundt,Alexander P.A. Stegmann,Bronwyn Kerr,Helen Kingston,Kate Chandler,Willow Sheehan,Abdallah F. Elias,Deepali N. Shinde,Meghan C. Towne,Nathaniel H. Robin,Dana H. Goodloe,Adeline Vanderver,Adeline Vanderver,Omar Sherbini,Krista Bluske,R. Tanner Hagelstrom,Caterina Zanus,Flavio Faletra,Luciana Musante,Evangeline Kurtz-Nelson,Rachel K. Earl,Britt-Marie Anderlid,Gilles Morin,Marjon van Slegtenhorst,Karin E. M. Diderich,Alice S. Brooks,Joost Gribnau,Ruben Boers,Teresa Robert Finestra,Lauren Carter,Anita Rauch,Paolo Gasparini,Paolo Gasparini,Kym M. Boycott,Tahsin Stefan Barakat,John M. Graham,Laurence Faivre,Siddharth Banka,Siddharth Banka,Tianyun Wang,Evan E. Eichler,Manuela Priolo,Bruno Dallapiccola,Lisenka E.L.M. Vissers,Bekim Sadikovic,Daryl A. Scott,Jimmy Holder,Marco Tartaglia +117 more
TL;DR: In this article, the authors used clinical data from 34 individuals with truncating variants in SPEN to define a neurodevelopmental disorder presenting with features that overlap considerably with those of proximal del1p36 syndrome.
Journal ArticleDOI
Inactivation of AMMECR1 is associated with growth, bone, and heart alterations.
Mariana Moysés-Oliveira,Mariana Moysés-Oliveira,Giuliana Giannuzzi,Richard J. Fish,Jill A. Rosenfeld,Florence Petit,Maria de Fátima de Faria Soares,Leslie Domenici Kulikowski,Adriana Di-Battista,Malú Zamariolli,Fan Xia,Thomas Liehr,Nadezda Kosyakova,Gianna Carvalheira,Michael W. Parker,Eleanor G. Seaby,Sarah Ennis,Rodney D. Gilbert,R. Tanner Hagelstrom,Maria L. Cremona,Wenhui L Li,Alka Malhotra,Anjana Chandrasekhar,Denise L. Perry,Ryan J. Taft,Julie McCarrier,Donald Basel,Joris Andrieux,Taiza Stumpp,Fernanda Antunes,Gustavo J.S. Pereira,Marguerite Neerman-Arbez,Vera Ayres Meloni,Margaret Drummond-Borg,Maria Isabel Melaragno,Alexandre Reymond +35 more
TL;DR: The results suggest that AMMECR1 is potentially involved in cell cycle control and linked to a new syndrome with growth, bone, heart, and kidney alterations with or without elliptocytosis.
Journal ArticleDOI
Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemia.
Yassmine Akkari,Helene Bruyere,R. Tanner Hagelstrom,Rashmi Kanagal-Shamanna,Jie Liu,Minjie Luo,Fady M. Mikhail,Beth A. Pitel,Gordana Raca,Mary Shago,Lina Shao,Lisa R. Smith,Teresa A. Smolarek,Ashwini Yenamandra,Linda B. Baughn +14 more
TL;DR: A comprehensive, evidence-based review of the current B-ALL literature, focusing on known and published subtypes described to date, describes the role of various testing modalities in the diagnosis, prognosis, and therapeutic relevance and proposes a testing algorithm aimed at assisting laboratories in the most effective detection of the underlying genomic abnormalities.