Angela M Bard

Years Active: 2023-2024
Publications (10 Years): 3

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

Publications

Angela M Bard, Lindsay V Clark, Erdal Cosgun, Kimberly A Aldinger, Andrew Timms, Lely A Quina, Juan M Lavista Ferres, David Jardine, Elisabeth A Haas, Tatiana M Becker, Chelsea M Pagan, Avni Santani, Diego Martinez, Soumitra Barua, Zakkary McNutt, Addie Nesbitt, Edwin A Mitchell, Jan-Marino Ramirez
Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing. American journal of medical genetics. Part A (2024)
Angela M Bard, Lindsay V Clark, Erdal Cosgun, Kimberly A Aldinger, Andrew Timms, Lely A Quina, Juan M Lavista Ferres, David Jardine, Elisabeth A Haas, Tatiana M Becker, Chelsea M Pagan, Avni Santani, Diego Martinez, Soumitra Barua, Zakkary McNutt, Addie Nesbitt, Edwin A Mitchell, Jan-Marino Ramirez
Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing. American journal of medical genetics. Part A (2024)
Angela M Bard, Lindsay V Clark, Erdal Cosgun, Kimberly A Aldinger, Andrew Timms, Lely A Quina, Juan M Lavista Ferres, David Jardine, Elisabeth A Haas, Tatiana M Becker, Chelsea M Pagan, Avni Santani, Diego Martinez, Soumitra Barua, Zakkary McNutt, Addie Nesbitt, Jan-Marino Ramirez
Known pathogenic gene variants and new candidates detected in Sudden Unexpected Infant Death (SUID) using Whole Genome Sequencing (WGS). medRxiv : the preprint server for health sciences (2023)

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