Austin Larson

ORCID

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 10

Top Venues

American journal of medical genetics. Part A

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

Publications

Jian Zhao, Nicola Longo, Robert G Lewis, Thomas J Nicholas, Steven E Boyden, Ashley Andrews, Austin Larson, null null, Pinar Bayrak-Toydemir, Lorenzo D Botto, Rong Mao
Novel molecular mechanism in Malan syndrome uncovered through genome sequencing reanalysis, exon-level Array, and RNA sequencing. American journal of medical genetics. Part A 194 (5) (2024)
Jian Zhao, Nicola Longo, Robert G Lewis, Thomas J Nicholas, Steven E Boyden, Ashley Andrews, Austin Larson, null null, Pinar Bayrak-Toydemir, Lorenzo D Botto, Rong Mao
Novel molecular mechanism in Malan syndrome uncovered through genome sequencing reanalysis, exon-level Array, and RNA sequencing. American journal of medical genetics. Part A 194 (5) (2024)
Jian Zhao, Nicola Longo, Robert G Lewis, Thomas J Nicholas, Steven E Boyden, Ashley Andrews, Austin Larson, null null, Pinar Bayrak-Toydemir, Lorenzo D Botto, Rong Mao
Novel molecular mechanism in Malan syndrome uncovered through genome sequencing reanalysis, exon-level Array, and RNA sequencing. American journal of medical genetics. Part A 194 (5) (2024)
Jian Zhao, Nicola Longo, Robert G Lewis, Thomas J Nicholas, Steven E Boyden, Ashley Andrews, Austin Larson, null null, Pinar Bayrak-Toydemir, Lorenzo D Botto, Rong Mao
Novel molecular mechanism in Malan syndrome uncovered through genome sequencing reanalysis, exon-level Array, and RNA sequencing. American journal of medical genetics. Part A (2024)
Jian Zhao, Nicola Longo, Robert G Lewis, Thomas J Nicholas, Steven E Boyden, Ashley Andrews, Austin Larson, null null, Pinar Bayrak-Toydemir, Lorenzo D Botto, Rong Mao
Novel molecular mechanism in Malan syndrome uncovered through genome sequencing reanalysis, exon-level Array, and RNA sequencing. American journal of medical genetics. Part A 194 (5) (2024)
Kristen Wigby, Monia Hammer, Mari Tokita, Priyanka Patel, Marilyn C Jones, Austin Larson, Frances Velez Bartolomei, Natalie Dykzeul, Anne M Slavotinek, Tiffany Yip, Sara Bandres-Ciga, Brittany N Simpson, Kristen Suhrie, Suma Shankar, Regan Veith, Jennifer Bragg, Cynthia Powell, Stephen F Kingsmore, David Dimmock, Jill Maron, Jonathan Davis, Miguel Del Campo
Insights into the perinatal phenotype of Kabuki syndrome in infants identified by genome-wide sequencing. American journal of medical genetics. Part A 191 (4) (2023)
Kristen Wigby, Monia Hammer, Mari Tokita, Priyanka Patel, Marilyn C Jones, Austin Larson, Frances Velez Bartolomei, Natalie Dykzeul, Anne M Slavotinek, Tiffany Yip, Sara Bandres-Ciga, Brittany N Simpson, Kristen Suhrie, Suma Shankar, Regan Veith, Jennifer Bragg, Cynthia Powell, Stephen F Kingsmore, David Dimmock, Jill Maron, Jonathan Davis, Miguel Del Campo
Insights into the perinatal phenotype of Kabuki syndrome in infants identified by genome-wide sequencing. American journal of medical genetics. Part A 191 (4) (2023)
Kristen Wigby, Monia Hammer, Mari Tokita, Priyanka Patel, Marilyn C Jones, Austin Larson, Frances Velez Bartolomei, Natalie Dykzeul, Anne M Slavotinek, Tiffany Yip, Sara Bandres-Ciga, Brittany N Simpson, Kristen Suhrie, Suma Shankar, Regan Veith, Jennifer Bragg, Cynthia Powell, Stephen F Kingsmore, David Dimmock, Jill Maron, Jonathan Davis, Miguel Del Campo
Insights into the perinatal phenotype of Kabuki syndrome in infants identified by genome-wide sequencing. American journal of medical genetics. Part A (2023)
Kristen Wigby, Monia Hammer, Mari Tokita, Priyanka Patel, Marilyn C Jones, Austin Larson, Frances Velez Bartolomei, Natalie Dykzeul, Anne M Slavotinek, Tiffany Yip, Sara Bandres-Ciga, Brittany N Simpson, Kristen Suhrie, Suma Shankar, Regan Veith, Jennifer Bragg, Cynthia Powell, Stephen F Kingsmore, David Dimmock, Jill Maron, Jonathan Davis, Miguel Del Campo
Insights into the perinatal phenotype of Kabuki syndrome in infants identified by genome-wide sequencing. American journal of medical genetics. Part A 191 (4) (2023)
Sara Gracie, Nivedita Sengupta, Carlos Ferreira, Joshua Pemberton, Ilse Anderson, Xin Wang, Lindsay Rhodes, Kathleen Brown, Tamas Balla, Austin Larson
De novo loss-of-function variant in PTDSS1 is associated with developmental delay. American journal of medical genetics. Part A 188 (6) (2022)

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Publication Activity (10 Years)

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Austin Larson