Neeta L Vora (Neeta Vora, Kate LaRiviere)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 39

Top Topics

Clinical Practice

Histone Deacetylase

Gene Expression

Congenital Heart Disease

Top Venues

Prenatal diagnosis

American journal of perinatology

bioRxiv : the preprint server for biology

Science advances

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

Publications

Neeta L Vora, Sylvie Langlois, Lyn S Chitty
Response to Wynn and Hokovec Regarding "The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use". Prenatal diagnosis (2024)
Emily Zhao, Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David Solowiejczyk, Neeta L Vora, Kelly L Gilmore, Jessica L Giordano, Ronald J Wapner, Simone Sanna-Cherchi, Alex Lyford, Angie C Jelin, Ali G Gharavi, Thomas Hays
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease. Prenatal diagnosis 44 (3) (2024)
Emily Zhao, Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David Solowiejczyk, Neeta L Vora, Kelly L Gilmore, Jessica L Giordano, Ronald J Wapner, Simone Sanna-Cherchi, Alex Lyford, Angie C Jelin, Ali G Gharavi, Thomas Hays
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease. Prenatal diagnosis 44 (3) (2024)
Emily Zhao, Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David Solowiejczyk, Neeta L Vora, Kelly L Gilmore, Jessica L Giordano, Ronald J Wapner, Simone Sanna-Cherchi, Alex Lyford, Angie C Jelin, Ali G Gharavi, Thomas Hays
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease. Prenatal diagnosis 44 (3) (2024)
Emily Zhao, Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David Solowiejczyk, Neeta L Vora, Kelly L Gilmore, Jessica L Giordano, Ronald J Wapner, Simone Sanna-Cherchi, Alex Lyford, Angie C Jelin, Ali G Gharavi, Thomas Hays
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease. Prenatal diagnosis 44 (3) (2024)
Emily Zhao, Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David Solowiejczyk, Neeta L Vora, Kelly L Gilmore, Jessica L Giordano, Ronald J Wapner, Simone Sanna-Cherchi, Alex Lyford, Angie C Jelin, Ali G Gharavi, Thomas Hays
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease. Prenatal diagnosis (2024)
Emily Zhao, Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David Solowiejczyk, Neeta L Vora, Kelly L Gilmore, Jessica L Giordano, Ronald J Wapner, Simone Sanna-Cherchi, Alex Lyford, Angie C Jelin, Ali G Gharavi, Thomas Hays
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease. Prenatal diagnosis 44 (3) (2024)
Emily Zhao, Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David Solowiejczyk, Neeta L Vora, Kelly L Gilmore, Jessica L Giordano, Ronald J Wapner, Simone Sanna-Cherchi, Alex Lyford, Angie C Jelin, Ali G Gharavi, Thomas Hays
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease. Prenatal diagnosis 44 (3) (2024)
Emily Zhao, Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David Solowiejczyk, Neeta L Vora, Kelly L Gilmore, Jessica L Giordano, Ronald J Wapner, Simone Sanna-Cherchi, Alex Lyford, Angie C Jelin, Ali G Gharavi, Thomas Hays
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease. Prenatal diagnosis (2024)
Emily Zhao, Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David Solowiejczyk, Neeta L Vora, Kelly L Gilmore, Jessica L Giordano, Ronald J Wapner, Simone Sanna-Cherchi, Alex Lyford, Angie C Jelin, Ali G Gharavi, Thomas Hays
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease. Prenatal diagnosis 44 (3) (2024)
Asha N Talati, Kelly L Gilmore, Emily E Hardisty, Anne D Lyerly, Christine Rini, Neeta L Vora
Diagnostic yield and psychological outcomes among women pursuing trio-exome sequencing: Do women with recurrent anomalous fetal phenotypes experience more negative psychological outcomes? Prenatal diagnosis (2023)
Naomi O Riches, 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. Prenatal diagnosis (2023)
Matthew R Grace, Neeta L Vora, Lisa Smeester, Sarah Dotters-Katz, Rebecca Fry, Victoria Bae-Jump, Kim Boggess
Sex-dependent differences in mouse placental gene expression following a maternal high fat diet. American journal of perinatology (2023)
Taylor N Takla, Jinghui Luo, Roksolana Sudyk, Joy Huang, J Clayton Walker, Neeta L Vora, Jonathan Z Sexton, Jack M Parent, Andrew M Tidball
A Shared Pathogenic Mechanism for Valproic Acid and SHROOM3 Knockout in a Brain Organoid Model of Neural Tube Defects. bioRxiv : the preprint server for biology (2023)
Lisa Hui, Katie Ellis, Dora Mayen, Mark Domenic Pertile, Rebecca Riemers, Lu-Ming Sun, Joris Robert Vermeesch, Neeta L Vora, Lyn S Chitty
Position statement from the International Society for Prenatal Diagnosis (ISPD) on the use of non-invasive prenatal testing (NIPT) for the detection of fetal chromosomal conditions in singleton pregnancies. Prenatal diagnosis (2023)
Taylor N Takla, Jinghui Luo, Roksolana Sudyk, Joy Huang, J Clayton Walker, Neeta L Vora, Jonathan Z Sexton, Jack M Parent, Andrew M Tidball
A Shared Pathogenic Mechanism for Valproic Acid and SHROOM3 Knockout in a Brain Organoid Model of Neural Tube Defects. bioRxiv : the preprint server for biology (2023)
Victoria Patterson, Farid Ullah, Laura Bryant, John N Griffin, Alpa Sidhu, Sheila Saliganan, Mackenzie Blaile, Margarita Sifuentes Saenz, Rosemarie Smith, Sara Ellingwood, Dorothy K Grange, Xuyun Hu, Maimaiti Mireguli, Yanfei Luo, Yiping Shen, Maureen S Mulhern, Elaine Zackai, Alyssa L Ritter, Kosaki Izumi, Julia Hoefele, Matias Wagner, Korbinian Maria Riedhammer, Barbara Seitz, Nathaniel H Robin, Dana Goodloe, Cyril Mignot, Boris Keren, Helen Cox, Joanna Jarvis, Maja Hempel, Cynthia Forster Gibson, Frédéric Tran Mau Them, Antonio Vitobello, Ange-Line Bruel, Arthur Sorlin, Sarju G Mehta, F Lucy Raymond, Kelly Gilmore, Bradford C Powell, Karen E Weck, Chumei Li, Anneke T Vulto-van Silfhout, Thea Giacomini, Maria Margherita Mancardi, Andrea Accogli, Vincenzo Salpietro, Federico Zara, Neeta L Vora, Erica E Davis, Rebecca D Burdine, Elizabeth Joyce Bhoj
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish. Science advances 9 (17) (2023)
Naomi O Riches, Erin P Johnson, Akila Subramaniam, Neeta L Vora, Emily Hardisty, Neeta L Vora, Erin Rothwell
Understanding the experiences and perspectives of prenatal screening among a diverse cohort. Prenatal diagnosis (2023)
Asha N Talati, Kelly L Gilmore, Emily E Hardisty, Anne D Lyerly, Christine Rini, Neeta L Vora
Diagnostic yield and psychological outcomes among women pursuing trio-exome sequencing: Do women with recurrent anomalous fetal phenotypes experience more negative psychological outcomes? Prenatal diagnosis (2023)
Sarah Harris, Manesha Putra, Kelly L Gilmore, Neeta L Vora
Two unrelated fetuses with ITPR1 missense variants and fetal hydrops. Prenatal diagnosis (2023)
Matthew R Grace, Neeta L Vora, Lisa Smeester, Sarah Dotters-Katz, Rebecca Fry, Victoria Bae-Jump, Kim Boggess
Sex-dependent differences in mouse placental gene expression following a maternal high fat diet. American journal of perinatology (2023)
Victoria Patterson, Farid Ullah, Laura Bryant, John N Griffin, Alpa Sidhu, Sheila Saliganan, Mackenzie Blaile, Margarita Sifuentes Saenz, Rosemarie Smith, Sara Ellingwood, Dorothy K Grange, Xuyun Hu, Maimaiti Mireguli, Yanfei Luo, Yiping Shen, Maureen S Mulhern, Elaine Zackai, Alyssa L Ritter, Kosaki Izumi, Julia Hoefele, Matias Wagner, Korbinian Maria Riedhammer, Barbara Seitz, Nathaniel H Robin, Dana Goodloe, Cyril Mignot, Boris Keren, Helen Cox, Joanna Jarvis, Maja Hempel, Cynthia Forster Gibson, Frédéric Tran Mau Them, Antonio Vitobello, Ange-Line Bruel, Arthur Sorlin, Sarju G Mehta, F Lucy Raymond, Kelly Gilmore, Bradford C Powell, Karen E Weck, Chumei Li, Anneke T Vulto-van Silfhout, Thea Giacomini, Maria Margherita Mancardi, Andrea Accogli, Vincenzo Salpietro, Federico Zara, Neeta L Vora, Erica E Davis, Rebecca D Burdine, Elizabeth Joyce Bhoj
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish. Science advances 9 (17) (2023)
Matthew R Grace, Neeta L Vora, Lisa Smeester, Sarah K Dotters-Katz, Rebecca C Fry, Victoria Bae-Jump, Kim Boggess
Sex-Dependent Differences in Mouse Placental Gene Expression following a Maternal High-Fat Diet. American journal of perinatology (2023)
Naomi O Riches, 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. Prenatal diagnosis (2023)
Matthew R Grace, Neeta L Vora, Lisa Smeester, Sarah K Dotters-Katz, Rebecca C Fry, Victoria Bae-Jump, Kim Boggess
Sex-Dependent Differences in Mouse Placental Gene Expression following a Maternal High-Fat Diet. American journal of perinatology (2023)
Taylor N Takla, Jinghui Luo, Roksolana Sudyk, Joy Huang, J Clayton Walker, Neeta L Vora, Jonathan Z Sexton, Jack M Parent, Andrew M Tidball
A Shared Pathogenic Mechanism for Valproic Acid and SHROOM3 Knockout in a Brain Organoid Model of Neural Tube Defects. bioRxiv : the preprint server for biology (2023)
Taylor N Takla, Jinghui Luo, Roksolana Sudyk, Joy Huang, John Clayton Walker, Neeta L Vora, Jonathan Z Sexton, Jack M Parent, Andrew M Tidball
A Shared Pathogenic Mechanism for Valproic Acid and SHROOM3 Knockout in a Brain Organoid Model of Neural Tube Defects. Cells 12 (13) (2023)
Taylor N Takla, Jinghui Luo, Roksolana Sudyk, Joy Huang, J Clayton Walker, Neeta L Vora, Jonathan Z Sexton, Jack M Parent, Andrew M Tidball
A Shared Pathogenic Mechanism for Valproic Acid and SHROOM3 Knockout in a Brain Organoid Model of Neural Tube Defects. bioRxiv : the preprint server for biology (2023)
Gillian V Blayney, Eoghan Laffan, Preethi A Jacob, Caitlin D Baptiste, Heinz Gabriel, Teresa N Sparks, Yuval Yaron, Mary E Norton, Karin E M Diderich, Yiming Wang, Karen Chong, David Chitayat, Neelam Saini, Shagun Aggarwal, Montse Pauta, Antoni Borrell, Kelly Gilmore, Natalie Jane Chandler, Stephanie K Allen, Neeta L Vora, Abdul Noor, Caitriona Monaghan, Mark David Kilby, Ronald J Wapner, Lyn S Chitty, Fionnuala Mone
Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis. Prenatal diagnosis (2023)
Neeta L Vora, Sylvie Langlois, Lyn S Chitty
Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use. Prenatal diagnosis (2023)
Asha N Talati, Kelly L Gilmore, Emily E Hardisty, Anne D Lyerly, Christine Rini, Neeta L Vora
Parental motivations for and adaptation to trio-exome sequencing in a prospective prenatal testing cohort: Beyond the diagnosis. Prenatal diagnosis 42 (6) (2022)
Bobby K Brar, Marisa Gilstrop Thompson, Neeta L Vora, Kelly Gilmore, Karin Blakemore, Kristen A Miller, Jessica L Giordano, Andreas Dufke, Beatrix Wong, Samantha Stover, Billie Lianoglou, Ignatia B Van den Veyver, Esther Dempsey, Mara Rosner, Karen Chong, David Chitayat, Teresa N Sparks, Mary E Norton, Ronald Wapner, Kristin Baranano, Angie C Jelin, null null
Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series. Prenatal diagnosis (2022)
Catherine G Kernie, Julia Wynn, Allison Rosenbaum, Jessica de Voest, Stephanie Galloway, Jessica L Giordano, Samantha Stover, Lauren Westerfield, Kelly Gilmore, Ronald J Wapner, Ignatia B Van den Veyver, Neeta L Vora, Rebecca G Clifton, Aaron B Caughey, Wendy K Chung
Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies. Prenatal diagnosis 42 (7) (2022)
Dayne L Filer, Piotr A Mieczkowski, Alicia Brandt, Kelly L Gilmore, Bradford C Powell, Jonathan S Berg, Kirk C Wilhelmsen, Neeta L Vora
Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fraction. Prenatal diagnosis (2021)
Kate Swanson, 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). Prenatal diagnosis (2021)
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
An approach to integrating exome sequencing for fetal structural anomalies into clinical practice. Genetics in medicine : official journal of the American College of Medical Genetics 22 (5) (2020)
Neeta L Vora, Emily Hardisty, Elizabeth Coviello, Alison Stuebe
Telehealth to provide prenatal genetics services: Feasibility and importance revealed during global pandemic. Prenatal diagnosis 40 (8) (2020)
Kathryn J Gray Guseh, Louise E Wilkins-Haug, Nancy J Herrig, Neeta L Vora
Fetal phenotypes emerge as genetic technologies become robust. Prenatal diagnosis 39 (9) (2019)
Sarah Harris, Kelly Gilmore, Emily Hardisty, Anne Drapkin Lyerly, Neeta L Vora
Ethical and counseling challenges in prenatal exome sequencing. Prenatal diagnosis 38 (12) (2018)