Kristen Rasmussen - Mayo Clinic - Rochester

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论文共 21 篇作者统计合作学者相似作者

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Impact of Integrated Translational Research on Clinical Exome Sequencing (vol 23, Pg 498, 2021)

Eric W. Klee,Margot A. Cousin, Filippo Pinto e Vairo, Joel A. Morales-Rosado,Erica L. Macke,W. Garrett Jenkinson,Alejandro Ferrer,Laura E. Schultz-Rogers,Rory J. Olson,Gavin R. Oliver,Ashley N. Sigafoos,Tanya L. Schwab, Michael T. Zimmermann,Raul A. Urrutia,Charu Kaiwar,Aditi Gupta, Patrick R. Blackburn,Nicole J. Boczek,Carri A. Prochnow, Rebecca J. Lowy,Lindsay A. Mulvihill,Tammy M. McAllister,Stacy L. Aoudia,Teresa M. Kruisselbrink,Lauren B. Gunderson,Jennifer L. Kemppainen, Laura J. Fisher,Jessica M. Tarnowski,Megan M. Hager,Sarah A. Kroc,Nicole L. Bertsch,Katherine E. Agre,Jessica L. Jackson, Sarah K. Macklin-Mantia, Marine I. Murphree,Laura M. Rust, Jolene M. Summer Bolster,Scott A. Beck,Paldeep S. Atwal,Marissa S. Ellingson,Sarah S. Barnett,Kristen J. Rasmussen,Carrie A. Lahner,Zhiyv Niu,Linda Hasadsri,Matthew J. Ferber,Cherisse A. Marcou, Karl J. Clark,Pavel N. Pichurin,David R. Deyle,Eva Morava-Kozicz, Ralitza H. Gavrilova, Radhika Dhamija,Klaas J. Wierenga,Brendan C. Lanpher, Dusica Babovic-Vuksanovic,Gianrico Farrugia, Lisa A. Schimmenti,A. Keith Stewart, Konstantinos N. Lazaridis

GENETICS IN MEDICINEno. 2 (2023)

引用0浏览0引用

The Landscape of Reported VUS in Multi-Gene Panel and Genomic Testing: Time for a Change

Heidi L. Rehm,Joseph T. Alaimo,Swaroop Aradhya,Pinar Bayrak-Toydemir,Hunter Best,Rhonda Brandon,Jillian G. Buchan,Elizabeth C. Chao,Elaine Chen,Jacob Clifford,Ana S. A. Cohen,Laura K. Conlin,Soma Das, Kyle W. Davis,Daniela del Gaudio,Florencia Del Viso,Christina Divincenzo,Marcia Eisenberg,Lucia Guidugli,Monia B. Hammer,Steven M. Harrison,Kathryn E. Hatchell, Lindsay Havens Dyer,Lily U. Hoang,James M. Holt,Vaidehi Jobanputra,Izabela D. Karbassi,Hutton M. Kearney,Melissa A. Kelly, Jacob M. Kelly,Michelle L. Kluge,Timothy Komala,Paul Kruszka,Lynette Lau,Matthew S. Lebo,Christian R. Marshall,Dianalee Mcknight,Kirsty Mcwalter, Yan Meng,Narasimhan Nagan, Christian S. Neckelmann,Nir Neerman,Zhiyv Niu,Vitoria K. Paolillo, Sarah A. Paolucci,Denise Perry,Tina Pesaran,Kelly Radtke,Kristen J. Rasmussen,Kyle Retterer,Carol J. Saunders,Elizabeth Spiteri,Christine Stanley,Anna Szuto,Ryan J. Taft,Isabelle Thiffault,Brittany C. Thomas,Amanda Thomas-Wilson,Erin Thorpe, Timothy J. Tidwell,Meghan C. Towne,Hana Zouk

Genetics in medicine official journal of the American College of Medical Geneticsno. 12 (2023): 100947-100947

引用3浏览0WOS引用

Impact of Integrated Translational Research on Clinical Exome Sequencing

Eric W. Klee,Margot A. Cousin,Filippo Pinto e Vairo,Joel A. Morales-Rosado,Erica L. Macke,W. Garrett Jenkinson,Alejandro Ferrer,Laura E. Schultz-Rogers,Rory J. Olson,Gavin R. Oliver,Ashley N. Sigafoos,Tanya L. Schwab,Michael T. Zimmermann,Raul A. Urrutia,Charu Kaiwar,Aditi Gupta,Patrick R. Blackburn,Nicole J. Boczek,Carri A. Prochnow, Rebecca J. Lowy,Lindsay A. Mulvihill,Tammy M. McAllister,Stacy L. Aoudia,Teresa M. Kruisselbrink,Lauren B. Gunderson,Jennifer L. Kemppainen, Laura J. Fisher,Jessica M. Tarnowski,Megan M. Hager,Sarah A. Kroc,Nicole L. Bertsch,Katherine E. Agre,Jessica L. Jackson,Sarah K. Macklin-Mantia,Marine Murphree,Laura M. Rust, Jolene M. Summer Bolster,Scott A. Beck,Paldeep S. Atwal,Marissa S. Ellingson,Sarah S. Barnett,Kristen J. Rasmussen,Carrie A. Lahner,Zhiyv Niu,Linda Hasadsri,Matthew J. Ferber,Cherisse A. Marcou,Karl J. Clark,Pavel N. Pichurin,David R. Deyle,Eva Morava-Kozicz,Ralitza H. Gavrilova,Radhika Dhamija,Klaas J. Wierenga,Brendan C. Lanpher,Dusica Babovic-Vuksanovic,Gianrico Farrugia,Lisa A. Schimmenti,A. Keith Stewart,Konstantinos N. Lazaridis

Genetics in medicine（2023）

引用22浏览0引用

Germline Variants in Tumor Suppressor FBXW7 Lead to Impaired Ubiquitination and a Neurodevelopmental Syndrome

Sarah E. M. Stephenson,Gregory Costain,Laura E. R. Blok,Michael A. Silk,Thanh Binh Nguyen,Xiaomin Dong, Dana E. Alhuzaimi,James J. Dowling,Susan Walker,Kimberly Amburgey, Robin Z. Hayeems, Lance H. Rodan, Marc A. Schwartz, Jonathan Picker, Sally A. Lynch, Aditi Gupta,Kristen J. Rasmussen,Lisa A. Schimmenti, Eric W. Klee,Zhiyv Niu,Katherine E. Agre, Ilana Chilton, Wendy K. Chung,Anya Revah-Politi, P. Y. Billie Au, Christopher Griffith, Melissa Racobaldo, Annick Raas-Rothschild, Bruria Ben Zeev, Ortal Barel,Sebastien Moutton, Fanny Morice-Picard, Virginie Carmignac, Jenny Cornaton,Nathalie Marle, Orrin Devinsky, Chandler Stimach,Stephanie Burns Wechsler, Bryan E. Hainline,Katie Sapp, Marjolaine Willems, Angeline Bruel, Kerith-Rae Dias, Carey-Anne Evans,Tony Roscioli,Rani Sachdev,Suzanna E. L. Temple, Ying Zhu, Joshua J. Baker,Ingrid E. Scheffer, Fiona J. Gardiner, Amy L. Schneider,Alison M. Muir, Heather C. Mefford,Amy Crunk, Elizabeth M. Heise,Francisca Millan, Kristin G. Monaghan,Richard Person,Lindsay Rhodes, Sarah Richards, Ingrid M. Wentzensen, Benjamin Cogne,Bertrand Isidor, Mathilde Nizon,Marie Vincent,Thomas Besnard, Amelie Piton, Carlo Marcelis, Kohji Kato, Norihisa Koyama, Tomoo Ogi, Elaine Suk-Ying Goh,Christopher Richmond, David J. Amor,Jessica O. Boyce,Angela T. Morgan,Michael S. Hildebrand, Antony Kaspi, Melanie Bahlo, Run Fridriksdottir,Hildigunnur Katrinardottir, Patrick Sulem, Kari Stefansson,Hans Tomas Bjornsson, Simone Mandelstam,Manuela Morleo, Milena Mariani,Marcello Scala, Andrea Accogli,Annalaura Torella, Valeria Capra, Mathew Wallis, Sandra Jansen, Quinten Waisfisz, Hugoline de Haan,Simon Sadedin,Sze Chern Lim, Susan M. White,David B. Ascher,Annette Schenck,Paul J. Lockhart,John Christodoulou,Tiong Yang Tan

The American Journal of Human Genetics（2022）

引用10浏览0WOS引用

A Second Cohort of CHD3 Patients Expands the Molecular Mechanisms Known to Cause Snijders Blok-Campeau Syndrome

Theodore G. Drivas, Dong Li,Divya Nair,Joseph T. Alaimo,Mariëlle Alders,Janine Altmüller,Tahsin Stefan Barakat,E. Martina Bebin,Nicole L. Bertsch,Patrick R. Blackburn,Alyssa Blesson,Arjan M. Bouman,Knut Brockmann,Perrine Brunelle,Margit Burmeister,Gregory M. Cooper,Jonas Denecke,Anne Dieux-Coëslier,Holly Dubbs,Alejandro Ferrer, Danna Gal,Lauren E. Bartik,Lauren B. Gunderson,Linda Hasadsri,Mahim Jain,Catherine Karimov,Beth Keena,Eric W. Klee,Katja Kloth,Baiba Lace,Marina Macchiaiolo,Julien L. Marcadier,Jeff M. Milunsky,Melanie P. Napier,Xilma R. Ortiz-Gonzalez,Pavel N. Pichurin,Jason Pinner,Zoe Powis,Chitra Prasad,Francesca Clementina Radio,Kristen J. Rasmussen,Deborah L. Renaud,Eric T. Rush,Carol Saunders,Duygu Selcen,Ann R. Seman,Deepali N. Shinde,Erica D. Smith,Thomas Smol,Lot Snijders Blok,Joan M. Stoler,Sha Tang,Marco Tartaglia,Michelle L. Thompson,Jiddeke M. van de Kamp,Jingmin Wang,Dagmar Weise,Karin Weiss,Rixa Woitschach,Bernd Wollnik,Huifang Yan,Elaine H. Zackai,Giuseppe Zampino,Philippe Campeau,Elizabeth Bhoj

European Journal of Human Genetics（2020）

引用19浏览0WOSNATURE引用

De Novo DDX3X Missense Variants in Males Appear Viable and Contribute to Syndromic Intellectual Disability

Pantelis Nicola,Patrick R. Blackburn,Kristen J. Rasmussen,Nicole L. Bertsch,Eric W. Klee,Linda Hasadsri,Pavel N. Pichurin,Julia Rankin,F. Lucy Raymond,Jill Clayton-Smith

American journal of medical genetics Part A（2019）

引用28浏览0WOS引用

Yield of Additional Genetic Testing after Chromosomal Microarray for Diagnosis of Neurodevelopmental Disability and Congenital Anomalies: a Clinical Practice Resource of the American College of Medical Genetics and Genomics (ACMG)

Darrel Waggoner,Karen E. Wain, Adrian M. Dubuc,Laura Conlin,Scott E. Hickey,Allen N. Lamb,Christa Lese Martin,Cynthia C. Morton,Kristen Rasmussen,Jane L. Schuette,Stuart Schwartz,David T. Miller

Genetics in medicineno. 10 (2018): 1105-1113

引用45浏览0WOS引用

Genetics of Familial Hypercholesterolemia

Ariel Brautbar,Emili Leary,Kristen Rasmussen,Don P. Wilson,Robert D. Steiner,Salim Virani

Current atherosclerosis reports（2015）

引用67浏览0WOS引用

Germline Activating Mtor Mutation Arising Through Gonadal Mosaicism in Two Brothers with Megalencephaly and Neurodevelopmental Abnormalities

Cameron Mroske,Kristen Rasmussen,Deepali N. Shinde,Robert Huether,Zoe Powis,Hsiao-Mei Lu,Ruth M. Baxter,Elizabeth McPherson,Sha Tang

BMC medical genetics（2015）

引用23浏览0WOS引用

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