Ruhma Syeda

ORCID

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 5

Top Venues

Nature communications

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

Publications

Nathalia G Amado, Elena D Nosyreva, David Thompson, Thomas J Egeland, Osita W Ogujiofor, Michelle Yang, Alexandria N Fusco, Niccolo Passoni, Jeremy Mathews, Brandi Cantarel, Linda A Baker, Ruhma Syeda
PIEZO1 loss-of-function compound heterozygous mutations in the rare congenital human disorder Prune Belly Syndrome. Nature communications 15 (1) (2024)
Nathalia G Amado, Elena D Nosyreva, David Thompson, Thomas J Egeland, Osita W Ogujiofor, Michelle Yang, Alexandria N Fusco, Niccolo Passoni, Jeremy Mathews, Brandi Cantarel, Linda A Baker, Ruhma Syeda
PIEZO1 loss-of-function compound heterozygous mutations in the rare congenital human disorder Prune Belly Syndrome. Nature communications 15 (1) (2024)
Nathalia G Amado, Elena D Nosyreva, David Thompson, Thomas J Egeland, Osita W Ogujiofor, Michelle Yang, Alexandria N Fusco, Niccolo Passoni, Jeremy Mathews, Brandi Cantarel, Linda A Baker, Ruhma Syeda
PIEZO1 loss-of-function compound heterozygous mutations in the rare congenital human disorder Prune Belly Syndrome. Nature communications 15 (1) (2024)
Nathalia G Amado, Elena D Nosyreva, David Thompson, Thomas J Egeland, Osita W Ogujiofor, Michelle Yang, Alexandria N Fusco, Niccolo Passoni, Jeremy Mathews, Brandi Cantarel, Linda A Baker, Ruhma Syeda
PIEZO1 loss-of-function compound heterozygous mutations in the rare congenital human disorder Prune Belly Syndrome. Nature communications 15 (1) (2024)
Nathalia G Amado, Elena D Nosyreva, David Thompson, Thomas J Egeland, Osita W Ogujiofor, Michelle Yang, Alexandria N Fusco, Niccolo Passoni, Jeremy Mathews, Brandi Cantarel, Linda A Baker, Ruhma Syeda
PIEZO1 loss-of-function compound heterozygous mutations in the rare congenital human disorder Prune Belly Syndrome. Nature communications 15 (1) (2024)

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Publication Activity (10 Years)

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Ruhma Syeda