Researcher
James Lawlor
HudsonAlpha Institute for Biotechnology
Statistics
33 papers found
All papers authored by James Lawlor
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Emily C. Gimpel,
Katelyn C. McNamara,
Carla A. Rich,
Candice R. Finnila,
Meagan E. Cochran,
James M. J. Lawlor ,
Kelly M. East,
Kevin M. Bowling,
Donald R. Latner,
Susan M. Hiatt,
Michelle D. Amaral,
Whitley V. Kelley,
Veronica Greve
and 26 other authors
Parents’ Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit
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Jared W. Taylor ,
Meagan Cochran,
James M. J. Lawlor ,
Belle A. Moyers,
Michelle D. Amaral,
Zachary T. Bonnstetter ,
Princess Carter,
Veronika Solomon,
Richard M. Myers ,
Marissa Natelson Love ,
David S. Geldmacher ,
Sara J. Cooper ,
Erik D. Roberson ,
J. Nicholas Cochran
Contributions of rare and common variation to early-onset and atypical dementia risk
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,
Susan M. Hiatt,
Michelle L. Thompson,
Donald R. Latner,
Candice R. Finnila,
Kevin M. Bowling,
Zachary T. Bonnstetter,
Katherine E. Bonini ,
Nicole R. Kelly,
Whitley V. Kelley,
Anna Ce E. Hurst,
Salman Rashid,
Melissa A. Kelly,
Ghunwa Nakouzi
and 5 other authors
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,
Thomas May,
Mariko Nakano-Okuno,
Tiffany Osborne
and 7 other authors
P392: Genomic medicine and primary care: The Alabama Genomic Health Initiative*
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Kelly M. East,
Meagan E. Cochran,
Veronica Greve,
Whitley V. Kelley,
David E. Gray,
Stephanie A. Felker,
Hannah Meddaugh,
Ashley Cannon
and 24 other authors
Genome sequencing as a first-line diagnostic test for hospitalized infants
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,
Lori Handley,
Zachary Bonnstetter,
Jerry Jenkins,
John Lovell,
James Holt,
Candice Finnila,
Michelle Thompson,
Donald Latner,
Christopher Partridge,
Christopher Plott,
Lori Beth Boston,
Melissa Williams,
Kevin Bowling
and 3 other authors
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,
Kelly East,
Meagan Cochran,
Veronica Greve,
Whitley V. Kelley,
David Gray,
Stephanie Felker,
Hannah Meddaugh,
Ashley Cannon
and 24 other authors
eP370: SouthSeq: Genome sequencing for a diverse population of hospitalized infants
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eP425: Parental impact of genome sequencing during the neonatal period
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and 9 other authors
eP494: Integration of genomics into primary care via the Alabama Genomic Health Initiative
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,
Gabriella “Ella” Balasa,
Miriam F. Figueira,
Francis “Tré” J LaRosa,
James M. J. Lawlor
Coming Full Circle: Reflections and Inspirations from a Cystic Fibrosis Patient Scientist Panel
Download from journals.sagepub.com
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Carla Rich,
Kelly M. East,
Whitley V. Kelley,
Shirley Simmons,
Candice R. Finnila,
Kevin Bowling,
Michelle Amaral,
Susan M. Hiatt,
Michelle Thompson,
David E. Gray,
James M. J. Lawlor ,
Richard M. Myers,
Gregory S. Barsh,
Edward J. Lose
and 3 other authors
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,
Lori H. Handley,
Ryne C. Ramaker,
Brianne B. Rogers,
E. Christopher Partridge,
E. Christopher Partridge,
Lori Beth Boston,
Melissa Williams,
Christopher B. Plott,
Jerry Jenkins,
David E. Gray,
James M. Holt,
Kevin M. Bowling,
E. Martina Bebin
and 4 other authors
Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders
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,
Kelly Williams,
Kelly M. East,
Whitley V. Kelley,
Irene P. Moss,
Devin M. Absher,
E. Christopher Partridge,
Anna C. E. Hurst,
Jeffrey C. Edberg,
Gregory S. Barsh,
Bruce R. Korf,
Gregory M. Cooper
Download from www.nature.com
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Xiaopeng Li,
John N. Schuen,
Susan L. Millard,
Xi Zhang,
Leah Buck,
Bethany Grysko,
Katie L. Uhl,
David Hinds,
Cynthia L. Stenger,
Michele Morris,
Neil Lamb,
Hara Levy,
Caleb Bupp
and 1 other authors
Genomic, transcriptomic, and protein landscape profile of CFTR and cystic fibrosis
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