Cynthia Curry

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Bio

She continues to be active in both clinical and academic genetics. Her research interests include syndrome delineation in the fetus and newborn, and causes of intellectual disability. She has held many national positions in both genetics and pediatrics and speaks nationally and internationally..

Research Interests

Papers共 143 篇Author StatisticsCo-AuthorSimilar Experts

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Ultra-rare Neurodevelopmental Disorder with Degenerative Course and Progressivemovement Disorders Associated with Biallelic ZBTB11 Variants

Juan Dario Ortigoza-Escobar,Mina Zamani,Dorison Nathalie,Saeid Sadeghian,Reza Azizimalamiri,Hamid Galehdari,Gholamreza Shariati,Alihossein Saberi,Seyed MohammadSaleh Zahraei, Niloofar Chamanrou,Andres Moreno-De-Luca,Lisette Leeuwen,Giovanni Zifarelli,Peter Bauer, Vincent d'Hardemare, Lydie Burglen,Diane Doummar,Cynthia Curry,Henry Houlden,Reza Maroofian

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 191-192

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Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders

MOVEMENT DISORDERS (2024)

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The Phenotype of MEGF8-related Carpenter Syndrome (CRPT2) is Refined Through the Identification of Eight New Patients

Laura M. Watts,Marta Bertoli,Tania Attie-Bitach, Natalie Roux,Antonio Rausell,Cate R. Paschal,Jessica L. Zambonin,Cynthia J. Curry, Blanche Martin,Rebecca S. Tooze,Lara Hawkes,Usha Kini,Stephen R. F. Twigg,Andrew O. M. Wilkie

EUROPEAN JOURNAL OF HUMAN GENETICSno. 7 (2024): 864-870

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Personal Journeys to and in Human Genetics and Dysmorphology

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 6 (2024)

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Diagnostic Yield of Pediatric and Prenatal Exome Sequencing in a Diverse Population

Anne Slavotinek,Shannon Rego,Nuriye Sahin-Hodoglugil,Mark Kvale,Billie Lianoglou,Tiffany Yip,Hannah Hoban,Simon Outram, Beatrice Anguiano,Flavia Chen,Jeremy Michelson,Roberta M. Cilio,Cynthia Curry,Renata C. Gallagher, Marisa Gardner,Rachel Kuperman,Bryce Mendelsohn,Elliott Sherr,Joseph Shieh,Jonathan Strober,Allison Tam,Jessica Tenney, William Weiss,Amy Whittle, Garrett Chin,Amanda Faubel,Hannah Prasad,Yusuph Mavura,Jessica Van Ziffle,W. Patrick Devine, Ugur Hodoglugil,Pierre-Marie Martin,Teresa N. Sparks,Barbara Koenig,Sara Ackerman, Neil Risch, Pui-Yan Kwok,Mary E. Norton

NPJ GENOMIC MEDICINE（2023）

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Deleterious, Protein-Altering Variants in the Transcriptional Coregulator ZMYM3 in 27 Individuals with a Neurodevelopmental Delay Phenotype

Susan M. Hiatt,Slavica Trajkova,Matteo Rossi Sebastiano,E. Christopher Partridge,Fatima E. Abidi,Ashlyn Anderson,Muhammad Ansar,Stylianos E. Antonarakis,Azadeh Azadi,Ruxandra Bachmann-Gagescu,Andrea Bartuli,Caroline Benech,Jennifer L. Berkowitz,Michael J. Betti,Alfredo Brusco,Ashley Cannon,Giulia Caron,Yanmin Chen,Meagan E. Cochran,Tanner F. Coleman,Molly M. Crenshaw,Laurence Cuisset,Cynthia J. Curry,Hossein Darvish,Serwet Demirdas,Maria Descartes,Jessica Douglas,David A. Dyment,Houda Zghal Elloumi,Giuseppe Ermondi,Marie Faoucher,Emily G. Farrow,Stephanie A. Felker,Heather Fisher,Anna C. E. Hurst,Pascal Joset,Melissa A. Kelly,Stanislav Kmoch, Benjamin R. Leadem,Michael J. Lyons,Marina Macchiaiolo,Martin Magner,Giorgia Mandrile,Francesca Mattioli,Megan McEown,Sarah K. Meadows,Livija Medne,Naomi J. L. Meeks,Sarah Montgomery, Melanie P. Napier,Marvin Natowicz,Kimberly M. Newberry,Marcello Niceta,Lenka Noskova,Catherine B. Nowak,Amanda G. Noyes,Matthew Osmond,Eloise J. Prijoles,Jada Pugh,Verdiana Pullano,Chloe Quelin,Simin Rahimi-Aliabadi,Anita Rauch,Sylvia Redon,Alexandre Reymond,Caitlin R. Schwager,Elizabeth A. Sellars,Angela E. Scheuerle, Elena Shukarova-Angelovska,Cara Skraban,Elliot Stolerman,Bonnie R. Sullivan,Marco Tartaglia,Isabelle Thiffault,Kevin Uguen,Luis A. Umana,Yolande van Bever,Saskia N. van der Crabben,Marjon A. van Slegtenhorst,Quinten Waisfisz,Camerun Washington,Lance H. Rodan,Richard M. Myers,Gregory M. Cooper

American journal of human genetics（2023）

Cited4Views0WOSBibtex

Ear Anomalies and Hearing Loss in Patients with VACTERL Association and the Effect of Maternal Diabetes

Carolina I. Galarreta,Erin Hoyt, Laura Forero,Cynthia J. Curry,Lynne M. Bird

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2023)

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Deleterious, protein-altering variants in the X-linked transcriptional coregulator ZMYM3 in 22 individuals with a neurodevelopmental delay phenotype

Susan M. Hiatt,Slavica Trajkova,Matteo Rossi Sebastiano,E. Christopher Partridge,Fatima E. Abidi,Ashlyn Anderson,Muhammad Ansar,Stylianos E. Antonarakis,Azadeh Azadi,Ruxandra Bachmann-Gagescu,Andrea Bartuli,Caroline Benech,Jennifer L. Berkowitz,Michael J. Betti,Alfredo Brusco,Ashley Cannon,Giulia Caron,Yanmin Chen,Molly M. Crenshaw,Laurence Cuisset,Cynthia J. Curry,Hossein Darvish,Serwet Demirdas,Maria Descartes,Jessica Douglas,David A. Dyment,Houda Zghal Elloumi,Giuseppe Ermondi,Marie Faoucher,Emily G. Farrow,Stephanie A. Felker,Heather Fisher,Anna C. E. Hurst,Pascal Joset,Stanislav Kmoch, Benjamin R. Leadem,Marina Macchiaiolo,Martin Magner,Giorgia Mandrile,Francesca Mattioli,Megan McEown,Sarah K. Meadows,Livija Medne,Naomi J. L. Meeks,Sarah Montgomery,Melanie P. Napier,Marvin Natowicz,Kimberly M. Newberry,Marcello Niceta,Lenka Noskova,Catherine Nowak,Amanda G. Noyes,Matthew Osmond,Verdiana Pullano,Chloé Quélin,Simin Rahimi-Aliabadi,Anita Rauch,Sylvia Redon,Alexandre Reymond,Caitlin R. Schwager,Elizabeth A. Sellars,Angela Scheuerle, Elena Shukarova-Angelovska,Cara Skraban,Bonnie R. Sullivan,Marco Tartaglia,Isabelle Thiffault,Kevin Uguen,Luis A. Umaña,Yolande van Bever,Saskia N. van der Crabben,Marjon A. van Slegtenhorst,Quinten Waisfisz,Richard M. Myers,Gregory M. Cooper

medrxiv（2022）

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Professor Emerita

Papers共 143 篇Author StatisticsCo-AuthorSimilar Experts