Morel Dayna - Miller School of Medicine, University of Miami

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论文共 13 篇作者统计合作学者相似作者

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Two Novel Heterozygous Exonic Deletions Lead to Chanarin-Dorfman Syndrome in a Patient with Congenital Ichthyosis, Sensorineural Hearing Loss, and Liver Dysfunction

Sofia Zoullas,Dayna Morel,Faraz Zafeer,Paulo Borjas-Mendoza,Simon Angeli, Yi Zhou,Guney Bademci,Mustafa Tekin

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 4 (2024)

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P254: Exome Sequencing As a First-Tier Approach for Rare Forms of Syndromic Hearing Loss

Carson Smith,Dayna Morel,LéShon Peart,Memoona Ramzan,Mustafa Tekin

Genetics in Medicine Open (2024): 101150

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Expanding the Phenotype of ASXL3-related Syndrome: a Comprehensive Description of 45 Unpublished Individuals with Inherited and De Novo Pathogenic Variants in ASXL3 (vol 185A, Pg 3446, 2021)

Schaida Schirwani,Albaba J. Shadi,Deanna Alexis Carere,Maria J. Guillen Sacoto,Francisca Milan Zamora,Yue Si,Rachel Rabin,John Pappas,Deborah L. Renaud,Natalie Hauser,Evan Reid,Patricia Blanchet,Nichola Foulds,Abhijit Dixit,Richard Fisher,Ruth Armstrong,Bertrand Isidor,Benjamin Cogne,Samantha Schrier Vergano,Serwet Demirdas,Natalie Dykzeul,Julie S. Cohen,Katheryn Grand,Dayna Morel,Anne Slavotinek,Hessa F. Albassam,Swati Naik,John Dean,Nicola Ragge,Cinzia Costa,Maria Giovanna Tedesco,Rachel E. Harrison,Arjan Bouman,Emily Palen,Thomas D. Challman,Marjolein H. Willemsen,Julie Vogt,Christopher Cunniff,Katherine Bergstrom,Jagdeep S. Walia,Ange-Line Bruel,Usha Kini,Fowzan S. Alkuraya,Valerie Slegesky,Naomi Meeks,Paula Girotto,Diana Johnson,Ruth Newbury-Ecob,Charlotte W. Ockeloen,Paolo Prontera,Sally Ann Lynch,Dong Li,John M. Graham,Tyler Mark Pierson,Meena Balasubramanian

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 1 (2023): 310-310

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Deletion of First Noncoding Exon in ANKRD11 Leads to KBG Syndrome

Nicholas Borja,Mohammad Faraz Zafeer,Jeimy Alfonso Rodriguez,Dayna Morel Swols,Willa Thorson,Guney Bademci,Mustafa Tekin

American journal of medical genetics Part Ano. 4 (2023): 1044-1049

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Dispersed DNA Variants Underlie Hearing Loss in South Florida’s Minority Population

LéShon Peart,Joanna Gonzalez,Dayna Morel Swols,Duygu Duman, Turcin Saridogan,Memoona Ramzan,Mohammad Faraz Zafeer,Xue Zhong Liu,Adrien A. Eshraghi,Michael E. Hoffer,Simon I. Angeli,Guney Bademci,Susan Blanton,Carson Smith,Fred F. Telischi,Mustafa Tekin

Human genomicsno. 1 (2023): 103-103

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Expanding the Phenotype of ASXL3-related Syndrome: A Comprehensive Description of 45 Unpublished Individuals with Inherited and De Novo Pathogenic Variants in ASXL3

Schaida Schirwani,Shadi Albaba,Deanna Alexis Carere,Maria J. Guillen Sacoto,Francisca Milan Zamora,Yue Si,Rachel Rabin,John Pappas,Deborah L. Renaud,Natalie Hauser,Evan Reid,Patricia Blanchet,Nichola Foulds,Abhijit Dixit,Richard Fisher,Ruth Armstrong,Bertrand Isidor,Benjamin Cogne,Samantha Schrier Vergano,Serwet Demirdas,Natalie Dykzeul,Julie S. Cohen,Katheryn Grand,Dayna Morel,Anne Slavotinek,Hessa F. Albassam,Swati Naik,John Dean,Nicola Ragge,Costa Cinzia,Maria Giovanna Tedesco,Rachel E. Harrison,Arjan Bouman,Emily Palen,Thomas D. Challman,Marjolein H. Willemsen,Julie Vogt,Christopher Cunniff,Katherine Bergstrom,Jagdeep S. Walia,Ange-Line Bruel,Usha Kini,Fowzan S. Alkuraya,Valerie Slegesky,Naomi Meeks,Paula Girotto,Diana Johnson,Ruth Newbury-Ecob,Charlotte W. Ockeloen,Paolo Prontera,Sally Ann Lynch,Dong Li,John M. Graham,Meena Balasubramanian

American journal of medical genetics Part A（2021）

引用10浏览0WOS引用

Chimerism Involving a RB1 Pathogenic Variant in Monochorionic Dizygotic Twins with Twin–twin Transfusion Syndrome

Anna M. Armitage, Monica A. Kundra,Neda Ghiam,Paldeep S. Atwal,Dayna Morel,Kathleen S. Hruska,Rebecca Torene,Irman Forghani

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2021）

引用2浏览0WOS引用

Phenotypic Spectrum and Transcriptomic Profile Associated with Germline Variants in TRAF7

Laura Castilla-Vallmanya,Kaja K. Selmer,Clemantine Dimartino,Raquel Rabionet,Bernardo Blanco-Sanchez,Sandra Yang,Margot R. F. Reijnders, Antonie J. van Essen,Myriam Oufadem,Magnus D. Vigeland,Barbro Stadheim,Gunnar Houge,Helen Cox,Helen Kingston,Jill Clayton-Smith,Jeffrey W. Innis,Maria Iascone,Anna Cereda,Sara Gabbiadini,Wendy K. Chung,Victoria Sanders,Joel Charrow,Emily Bryant,John Millichap,Antonio Vitobello,Christel Thauvin,Frederic Tran Mau-Them,Laurence Faivre,Gaetan Lesca,Audrey Labalme,Christelle Rougeot,Nicolas Chatron,Damien Sanlaville,Katherine M. Christensen,Amelia Kirby,Raymond Lewandowski, Rachel Gannaway, Maha Aly,Anna Lehman,Lorne Clarke,Luitgard Graul-Neumann,Christiane Zweier,Davor Lessel,Bernarda Lozic,Ingvild Aukrust,Ryan Peretz,Robert Stratton,Thomas Smol,Anne Dieux-Coeslier,Joanna Meira,Elizabeth Wohler,Nara Sobreira,Erin M. Beaver,Jennifer Heeley,Lauren C. Briere,Frances A. High,David A. Sweetser,Melissa A. Walker,Catherine E. Keegan,Parul Jayakar,Marwan Shinawi,Wilhelmina S. Kerstjens-Frederikse,Dawn L. Earl,Victoria M. Siu,Emma Reesor,Tony Yao,Robert A. Hegele,Olena M. Vaske,Shannon Rego,Kevin A. Shapiro, Brian Wong,Michael J. Gambello,Marie McDonald,Danielle Karlowicz,Roberto Colombo,Alessandro Serretti,Lynn Pais,Anne O'Donnell-Luria, Alison Wray,Simon Sadedin,Belinda Chong,Tiong Y. Tan,John Christodoulou,Susan M. White,Anne Slavotinek,Deborah Barbouth,Dayna Morel Swols,Melanie Parisot,Christine Bole-Feysot,Patrick Nitschke,Veronique Pingault,Arnold Munnich,Megan T. Cho,Valerie Cormier-Daire,Susanna Balcells,Stanislas Lyonnet,Daniel Grinberg,Jeanne Amiel,Roser Urreizti,Christopher T. Gordon

Genetics in medicine（2020）

引用16浏览0WOS引用

Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida

Saradadevi Thanikachalam,Elizabeth Hodapp,Ta C. Chang,Dayna Morel Swols,Filiz B. Cengiz,Shengru Guo,Mohammad F. Zafeer,Serhat Seyhan,Guney Bademci,William K. Scott,Alana Grajewski,Mustafa Tekin

Genes（2020）

引用15浏览0WOS引用

Autosomal Dominant Inheritance in a Recently Described ZMIZ1-related Neurodevelopmental Disorder: Case Report of Siblings and an Affected Parent

Kumarie Latchman, Madison Calder,Dayna Morel,Lindsay Rhodes,Jane Juusola,Mustafa Tekin

American journal of medical genetics Part A（2019）

引用6浏览0WOS引用

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