McKnight Dianalee A - NIDCR, NIH | 人才画像

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论文共 91 篇作者统计合作学者相似作者

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Early Genetic Testing in Pediatric Epilepsy: Diagnostic and Cost Implications

Shanna M. Swartwood,Ana Morales,Kathryn E. Hatchell,Chad Moretz,Dianalee McKnight,Laurie Demmer, Sarah Chagnon,Swaroop Aradhya,Edward D. Esplin,Joshua L. Bonkowsky

EPILEPSIA OPENno. 1 (2024): 439-444

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P537: Reliability of clinician entries for patient self-identified race, ethnicity, and ancestry in clinical genetic testing

Alice Popejoy,Ana Morales,Dianalee McKnight

Genetics in Medicine Openno. 1 (2023): 100584-100584

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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

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Genetic testing outcomes in a cohort of 21,159 children with heart disease

Robert Nussbaum,Flavia Facio,Ana Morales,Asia Mitchell,John Garcia,Dianalee McKnight,Tom Callis,Chad Moretz,Matteo Vatta,Swaroop Aradhya

Heart, Lung and Circulation (2023): 410-411

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THE IMPACT OF MACHINE LEARNING MODELS IN REDUCING VARIANTS OF UNCERTAIN SIGNIFICANCE (VUS) FOR INDIVIDUALS FROM UNDERREPRESENTED POPULATIONS WHO ARE UNDERGOING TESTING FOR INHERITED METABOLIC DISORDERS

Britt Johnson,Flavia Facio,Ana Morales,Laure Fresard,Dianalee McKnight,Yuya Kobayashi,Jason Reuter,Swaroop Aradhya,Keith Nykamp,Alexandre Colavin

MOLECULAR GENETICS AND METABOLISM（2023）

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Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing

Elaine Chen,Flavia M. Facio,Kerry W. Aradhya,Susan Rojahn,Kathryn E. Hatchell,Sienna Aguilar,Karen Ouyang,Sulagna Saitta, Andrea K. Hanson-Kwan, Nicole Nakousi Capurro,Eriko Takamine,Saumya Shekhar Jamuar,Dianalee McKnight,Britt Johnson,Swaroop Aradhya

JAMA NETWORK OPENno. 10 (2023)

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Racial and Ethnic Differences in the Diagnostic Yield of Cardiomyopathy, Aortopathy, and Arrhythmia Genetic Testing and Frequency of Family Variant Screening

Spencer V. Carter, Justin L. Grodin,Vicente Morales Oyarvide, Eric D. Peterson,Sadiya S. Khan,Dianalee McKnight,Ana Morales,Emily Russell,Yi-Lee Ting,Ann Marie M. Navar

CIRCULATION (2023)

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Abstract 13352: the Impact of Machine Learning Models in Reducing Variants of Uncertain Significance in Individuals from Underrepresented Populations Who Are Undergoing Genetic Testing for Heritable Heart Conditions

Ana Morales,Britt Johnson,Flavia Facio,Yi-Lee Ting,Matteo Vatta,Laure Fresard,Dianalee McKnight,Yuya Kobayashi,Jason Reuter,Swaroop Aradhya,Keith Nykamp,Alexandre Colavin

CIRCULATION（2023）

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Computation of longitudinal phenotypes in 466 individuals with a developmental and epileptic encephalopathy enables clinical trial readiness

Elise Brimble,Joseph Kim,Richard L. Martin,Dianalee McKnight,Alix M. B. Lacoste

medRxiv (Cold Spring Harbor Laboratory) (2023)

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P276: Long-chain Fatty Acid Oxidation Disorder Genotypes, Clinical Signs and Symptoms, and Newborn Screening History from a Gene Panel Sponsored Program

Vanessa Rangel Miller,Omid Japalaghi,Nicola Longo,Deborah Marsden,Dianalee McKnight,Nicole Miller

Molecular genetics and metabolism（2023）

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