Alanna Strong

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 19

Top Venues

American journal of medical genetics. Part A

Nature medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Alanna Strong, Soumya Rao, Sandra von Hardenberg, Dong Li, Liza L Cox, Paul C Lee, Li Q Zhang, Waheed Awotoye, Tamir Diamond, Jessica Gold, Catherine Gooch, Lord Jephthah Joojo Gowans, Hakon Hakonarson, Anne Hing, Kathleen Loomes, Nicole Martin, Mary L Marazita, Tarja Mononen, David Piccoli, Rolph Pfundt, Salmo Raskin, Stephen W Scherer, Nara Lygia de Macena Sobreira, Courtney Vaccaro, Xiang Wang, Deborah Watson, Rosanna Weksberg, Elizabeth Bhoj, Jeffrey C Murray, Andrew C Lidral, Azeez Butali, Michael F Buckley, Tony Roscioli, David A Koolen, Laurie H Seaver, Cynthia A Prows, Rolf W Stottmann, Timothy C Cox
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature. American journal of medical genetics. Part A (2023)
Helen M Stanley, Brian R White, Christopher J LaRosa, Mark W Cocalis, J William Gaynor, Alanna Strong, Balram Gangaram
Patent ductus arteriosus and coarctation of the aorta in association with PRDM6 variants. American journal of medical genetics. Part A (2023)
Alanna Strong
CRISPR gene-editing therapies for hypertrophic cardiomyopathy. Nature medicine (2023)
Alanna Strong
CRISPR gene-editing therapies for hypertrophic cardiomyopathy. Nature medicine 29 (2) (2023)
Alanna Strong
CRISPR gene-editing therapies for hypertrophic cardiomyopathy. Nature medicine 29 (2) (2023)
Alanna Strong
CRISPR gene-editing therapies for hypertrophic cardiomyopathy. Nature medicine 29 (2) (2023)
Alanna Strong, Hui-Qi Qu, Sinéad Cullina, Morgan L McManus, Elaine H Zackai, Joseph Glessner, Eimear E Kenny, Hakon H Hakonarson
TOPORS as a novel causal gene for Joubert syndrome. American journal of medical genetics. Part A (2023)
Alanna Strong
CRISPR gene-editing therapies for hypertrophic cardiomyopathy. Nature medicine 29 (2) (2023)
Alanna Strong
CRISPR gene-editing therapies for hypertrophic cardiomyopathy. Nature medicine 29 (2) (2023)
Alanna Strong, Soumya Rao, Sandra von Hardenberg, Dong Li, Liza L Cox, Paul C Lee, Li Q Zhang, Waheed Awotoye, Tamir Diamond, Jessica Gold, Catherine Gooch, Lord Jephthah Joojo Gowans, Hakon Hakonarson, Anne Hing, Kathleen Loomes, Nicole Martin, Mary L Marazita, Tarja Mononen, David Piccoli, Rolph Pfundt, Salmo Raskin, Stephen W Scherer, Nara Lygia de Macena Sobreira, Courtney Vaccaro, Xiang Wang, Deborah Watson, Rosanna Weksberg, Elizabeth Bhoj, Jeffrey C Murray, Andrew C Lidral, Azeez Butali, Michael F Buckley, Tony Roscioli, David A Koolen, Laurie H Seaver, Cynthia A Prows, Rolf W Stottmann, Timothy C Cox
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature. American journal of medical genetics. Part A (2023)
Guozhuang Li, Alanna Strong, Haojun Wang, Ji-Sun Kim, Deborah Watson, Sen Zhao, Courtney Vaccaro, Erum Hartung, Hakon H Hakonarson, Terry Jianguo Zhang, Philip F Giampietro, Nan Wu
TBX6 as a cause of a combined skeletal-kidney dysplasia syndrome. American journal of medical genetics. Part A 188 (12) (2022)
Jacklyn Omorodion, Leah Dowsett, Robin D Clark, Jamie Fraser, Aya Abu-El-Haija, Alanna Strong, Monica H Wojcik, Allison S Bryant, Nina B Gold
Delayed diagnosis and racial bias in children with genetic conditions. American journal of medical genetics. Part A 188 (4) (2022)
Alanna Strong, Laurie Simone, Anthony Krentz, Courtney Vaccaro, Deborah Watson, Hayley Ron, Jennifer M Kalish, Helio F Pedro, Elaine H Zackai, Hakon H Hakonarson
Expanding the genetic landscape of oral-facial-digital syndrome with two novel genes. American journal of medical genetics. Part A 185 (8) (2021)
Alanna Strong, Cara M Skraban, Kevin Meyers, Sandra Amaral, Susan Furth, Stacey Drant, Wendy Hsiao, Lauren Galea, Jessica Gold, Nina B Gold, Jacqueline Leonard, Sonya Lopez, Elaine H Zackai, Reed E Pyeritz
Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypes. American journal of medical genetics. Part A 185 (12) (2021)
Alanna Strong, Dong Li, Frank Mentch, Hakon H Hakonarson
A novel heterotaxy gene: Expansion of the phenotype of TTC21B-spectrum disease. American journal of medical genetics. Part A 185 (4) (2021)
Alanna Strong, Gina O'Grady, Evelyn Shih, Jonathan R Bishop, Kathleen Loomes, Tamir Diamond, Erum A Hartung, William Wong, Sanmati Cuddapah, Anne Marie Cahill, Cuiping Hou, Diana Slater, Courtney Vaccaro, Deborah Watson, Dong Li, Hakon H Hakonarson
A new syndrome of moyamoya disease, kidney dysplasia, aminotransferase elevation, and skin disease associated with de novo variants in RNF213. American journal of medical genetics. Part A 185 (7) (2021)
Alanna Strong, Michael E March, Christopher J Cardinale, Sophia E Kim, Jamie Merves, Hilary Whitworth, Leslie Raffini, Christopher Larosa, Lawrence Copelovitch, Cuiping Hou, Diana Slater, Courtney Vaccaro, Deborah Watson, Elaine H Zackai, Jeffrey Billheimer, Hakon H Hakonarson
A novel MBTPS2 variant associated with BRESHECK syndrome impairs sterol-regulated transcription and the endoplasmic reticulum stress response. American journal of medical genetics. Part A (2021)
Alanna Strong, Dong Li, Frank Mentch, Emma C Bedoukian, Erum A Hartung, Kevin Meyers, Cara M Skraban, Jessica Wen, Livija Medne, Joseph Glessner, Deborah Watson, Ian Krantz, Hakon H Hakonarson
Ciliopathies: Coloring outside of the lines. American journal of medical genetics. Part A 185 (3) (2020)
Alanna Strong, Samina Muneeruddin, Richard Parrish, Daniel Lui, Susan B Conley
Isosorbide dinitrate in nephronophthisis treatment. American journal of medical genetics. Part A 176 (4) (2019)

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Publication Activity (10 Years)

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Alanna Strong