Papers authored by Neeta Vora
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Taylor N. Takla,
John Clayton Walker,
Jinghui Luo,
Roksolana Sudyk,
Joy Huang,
J. Clayton Walker,
Neeta L. Vora 
,
Jonathan Z. Sexton,
Jack M. Parent,
Andrew M. Tidball
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,
Jonathan Z. Sexton,
Jack M. Parent,
Andrew M. Tidball
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Lisa Hui ,
Katie Ellis,
Dora Mayen,
Mark D. Pertile ,
Rebecca Reimers ,
Luming Sun ,
Joris Vermeesch ,
Neeta L. Vora ,
Lyn S. Chitty
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,
Katie Ellis,
Dora Mayen,
Mark D. Pertile ,
Rebecca Reimers ,
Luming Sun ,
Joris Vermeesch ,
Neeta L. Vora ,
Lyn S. Chitty
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Victoria Patterson ,
Farid Ullah ,
Laura Bryant ,
Dong Li,
John N. Griffin,
Alpa Sidhu ,
Sheila Saliganan,
Mackenzie Blaile,
Margarita S. Saenz ,
Rosemarie Smith,
Sara Ellingwood,
Dorothy K. Grange ,
Xuyun Hu ,
Maimaiti Mireguli,
Yanfei Luo
and 37 other authors
,
Farid Ullah ,
Laura Bryant ,
Dong Li,
John N. Griffin,
Alpa Sidhu ,
Sheila Saliganan,
Mackenzie Blaile,
Margarita S. Saenz ,
Rosemarie Smith,
Sara Ellingwood,
Dorothy K. Grange ,
Xuyun Hu ,
Maimaiti Mireguli,
Yanfei Luo
and 37 other authors
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish
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Asha N. Talati ,
Kelly L. Gilmore,
Emily E. Hardisty,
Anne D. Lyerly,
Christine Rini,
Neeta L. Vora
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,
Kelly L. Gilmore,
Emily E. Hardisty,
Anne D. Lyerly,
Christine Rini,
Neeta L. Vora
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Naomi O. Riches ,
Erin P. Johnson,
Akila Subramaniam,
Neeta L. Vora ,
Emily Hardisty,
Kate LaRiviere,
Erin Rothwell
,
Erin P. Johnson,
Akila Subramaniam,
Neeta L. Vora ,
Emily Hardisty,
Kate LaRiviere,
Erin Rothwell
Understanding the experiences and perspectives of prenatal screening among a diverse cohort
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2022
Bobby K. Brar,
Marisa Gilstrop Thompson,
Neeta L. Vora ,
Kelly Gilmore,
Karin Blakemore,
Kristen A. Miller,
Jessica Giordano,
Andreas Dufke,
Beatrix Wong,
Samantha Stover,
Billie Lianoglou,
Ignatia Van den Veyver,
Esther Dempsey,
Mara Rosner,
Karen Chong
and 6 other authors
,
Kelly Gilmore,
Karin Blakemore,
Kristen A. Miller,
Jessica Giordano,
Andreas Dufke,
Beatrix Wong,
Samantha Stover,
Billie Lianoglou,
Ignatia Van den Veyver,
Esther Dempsey,
Mara Rosner,
Karen Chong
and 6 other authors
Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series
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Asha N. Talati ,
Kelly L. Gilmore,
Emily E. Hardisty,
Anne D. Lyerly,
Christine Rini,
Neeta L. Vora
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,
Kelly L. Gilmore,
Emily E. Hardisty,
Anne D. Lyerly,
Christine Rini,
Neeta L. Vora
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2021
Kate Swanson ,
Juliet C. Bishop,
Huda B. Al‐Kouatly ,
Mona Makhamreh,
Thomas Felton,
Neeta L. Vora ,
Teresa N. Sparks ,
Angie C. Jelin
,
Juliet C. Bishop,
Huda B. Al‐Kouatly ,
Mona Makhamreh,
Thomas Felton,
Neeta L. Vora ,
Teresa N. Sparks ,
Angie C. Jelin
Prenatal phenotype of 47, XXY (Klinefelter syndrome)
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Dayne L. Filer ,
Piotr A. Mieczkowski,
Alicia Brandt,
Kelly L. Gilmore,
Bradford C. Powell,
Jonathan S. Berg,
Kirk C. Wilhelmsen,
Neeta L. Vora
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,
Piotr A. Mieczkowski,
Alicia Brandt,
Kelly L. Gilmore,
Bradford C. Powell,
Jonathan S. Berg,
Kirk C. Wilhelmsen,
Neeta L. Vora
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Neeta L. Vora ,
Kelly Gilmore,
Alicia Brandt,
Chelsea Gustafson,
Natasha Strande,
Lori Ramkissoon,
Emily Hardisty,
Ann Katherine M. Foreman,
Kirk Wilhelmsen,
Phillips Owen,
Karen E. Weck,
Jonathan S. Berg,
Cynthia M. Powell,
Bradford C. Powell
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Kelly Gilmore,
Alicia Brandt,
Chelsea Gustafson,
Natasha Strande,
Lori Ramkissoon,
Emily Hardisty,
Ann Katherine M. Foreman,
Kirk Wilhelmsen,
Phillips Owen,
Karen E. Weck,
Jonathan S. Berg,
Cynthia M. Powell,
Bradford C. Powell
An approach to integrating exome sequencing for fetal structural anomalies into clinical practice
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2019
Kathryn J. Gray ,
Louise E. Wilkins‐Haug ,
Nancy J. Herrig,
Neeta L. Vora
,
Louise E. Wilkins‐Haug ,
Nancy J. Herrig,
Neeta L. Vora
Fetal phenotypes emerge as genetic technologies become robust
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2017
Sunayna Best,
Karen Wou,
Neeta Vora ,
Ignatia B. Van der Veyver,
Ronald Wapner,
Lyn S. Chitty
,
Ignatia B. Van der Veyver,
Ronald Wapner,
Lyn S. Chitty
Promises, pitfalls and practicalities of prenatal whole exome sequencing
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