Vaidehi Jobanputra

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 20

Top Venues

NPJ genomic medicine

Circulation. Genomic and precision medicine

JCO precision oncology

Cold Spring Harbor molecular case studies

All India Institute of Medical Sciences (PHD)

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

Education History

All India Institute of Medical Sciences

India

PHD :: Anatomy

Publications

Kristen M Wigby, Deanna Brockman, Gregory Costain, Caitlin Hale, Stacie L Taylor, John W Belmont, David Bick, David P Dimmock, Susan Fernbach, John Greally, Vaidehi Jobanputra, Shashikant Kulkarni, Elizabeth Spiteri, Ryan J Taft
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders. NPJ genomic medicine 9 (1) (2024)
Kristen M Wigby, Deanna Brockman, Gregory Costain, Caitlin Hale, Stacie L Taylor, John W Belmont, David Bick, David P Dimmock, Susan Fernbach, John Greally, Vaidehi Jobanputra, Shashikant Kulkarni, Elizabeth Spiteri, Ryan J Taft
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders. NPJ genomic medicine 9 (1) (2024)
Vaidehi Jobanputra, Brock E Schroeder, Michael J Bamshad, Wei Shen, Elizabeth Spiteri, Ghunwa Nakouzi, Stacie L Taylor, Christian R Marshall, Linyan Meng, Stephen F Kingsmore, Katarzyna A Ellsworth, Euan Ashley, Ryan J Taft, null null
Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action. NPJ genomic medicine 9 (1) (2024)
Kristen M Wigby, Deanna Brockman, Gregory Costain, Caitlin Hale, Stacie L Taylor, John W Belmont, David Bick, David P Dimmock, Susan Fernbach, John Greally, Vaidehi Jobanputra, Shashikant Kulkarni, Elizabeth Spiteri, Ryan J Taft
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders. NPJ genomic medicine 9 (1) (2024)
Vaidehi Jobanputra, Brock E Schroeder, Michael J Bamshad, Wei Shen, Elizabeth Spiteri, Ghunwa Nakouzi, Stacie L Taylor, Christian R Marshall, Linyan Meng, Stephen F Kingsmore, Katarzyna A Ellsworth, Euan Ashley, Ryan J Taft, null null
Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action. NPJ genomic medicine 9 (1) (2024)
Thomas Hays, Rebecca Hernan, Michele Disco, Emily L Griffin, Nimrod Goldshtrom, Diana Vargas Chaves, Ganga Krishnamurthy, Miles Bomback, Atteeq U Rehman, Amanda L Thomas, Saurav Guha, Shruti Phadke, Volkan Okur, Dino Robinson, Vanessa Felice, Avinash Abhyankar, Vaidehi Jobanputra, Wendy K Chung
Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease. Circulation. Genomic and precision medicine (2023)
Emily L Griffin, Shannon N Nees, Sarah U Morton, Julia Wynn, Nihir Patel, Vaidehi Jobanputra, Scott Robinson, Stephanie M Kochav, Alice Tao, Carli Andrews, Nancy Cross, Judith Geva, Kristen Lanzilotta, Alyssa L Ritter, Eileen Taillie, Alexandra Thompson, Chris Meyer, Rachel Akers, Eileen C King, James F Cnota, Richard W Kim, George A Porter, Martina Brueckner, Christine E Seidman, Yufeng Shen, Bruce D Gelb, Elizabeth Goldmuntz, Jane W Newburger, Amy E Roberts, Wendy K Chung
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circulation. Genomic and precision medicine (2023)
Emily L Griffin, Shannon N Nees, Sarah U Morton, Julia Wynn, Nihir Patel, Vaidehi Jobanputra, Scott Robinson, Stephanie M Kochav, Alice Tao, Carli Andrews, Nancy Cross, Judith Geva, Kristen Lanzilotta, Alyssa L Ritter, Eileen Taillie, Alexandra Thompson, Chris Meyer, Rachel Akers, Eileen C King, James F Cnota, Richard W Kim, George A Porter, Martina Brueckner, Christine E Seidman, Yufeng Shen, Bruce D Gelb, Elizabeth Goldmuntz, Jane W Newburger, Amy E Roberts, Wendy K Chung
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circulation. Genomic and precision medicine (2023)
Matthew J Lewis, Alexander Hsieh, Lu Qiao, Renjie Tan, Brigitte Kazzi, Alexandra Channing, Emily L Griffin, Vaidehi Jobanputra, Jennifer Su, Chowdhury Shahryar, Lazaros K Kochilas, William Gaynor, Teresa Lee, Elizabeth Goldmuntz, Mark W Russell, Seema Mital, Martin Tristani-Firouzi, Martina Brueckner, Jane W Newburger, Yufeng Shen, Wendy K Chung
Association of Predicted Damaging De Novo Variants on Ventricular Function in Individuals With Congenital Heart Disease. Circulation. Genomic and precision medicine (2023)
Emily L Griffin, Shannon N Nees, Sarah U Morton, Julia Wynn, Nihir Patel, Vaidehi Jobanputra, Scott Robinson, Stephanie M Kochav, Alice Tao, Carli Andrews, Nancy Cross, Judith Geva, Kristen Lanzilotta, Alyssa L Ritter, Eileen Taillie, Alexandra Thompson, Chris Meyer, Rachel Akers, Eileen C King, James F Cnota, Richard W Kim, George A Porter, Martina Brueckner, Christine E Seidman, Yufeng Shen, Bruce D Gelb, Elizabeth Goldmuntz, Jane W Newburger, Amy E Roberts, Wendy K Chung
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circulation. Genomic and precision medicine (2023)
Emily L Griffin, Shannon N Nees, Sarah U Morton, Julia Wynn, Nihir Patel, Vaidehi Jobanputra, Scott Robinson, Stephanie M Kochav, Alice Tao, Carli Andrews, Nancy Cross, Judith Geva, Kristen Lanzilotta, Alyssa L Ritter, Eileen Taillie, Alexandra Thompson, Chris Meyer, Rachel Akers, Eileen C King, James F Cnota, Richard W Kim, George A Porter, Martina Brueckner, Christine E Seidman, Yufeng Shen, Bruce D Gelb, Elizabeth Goldmuntz, Jane W Newburger, Amy E Roberts, Wendy K Chung
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circulation. Genomic and precision medicine (2023)
Edwin Cuppen, Olivier Elemento, Richard Rosenquist, Svetlana Nikic, Maarten IJzerman, Isabelle Durand Zaleski, Geert Frederix, Lars-Åke Levin, Charles G Mullighan, Reinhard Buttner, Trevor J Pugh, Sean M Grimmond, Carlos Caldas, Fabrice Andre, Ilse Custers, Elias Campo, Hans van Snellenberg, Anna Schuh, Hidewaki Nakagawa, Christof von Kalle, Torsten Haferlach, Stefan Fröhling, Vaidehi Jobanputra
Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care. JCO precision oncology 6 (2022)
Edwin Cuppen, Olivier Elemento, Richard Rosenquist, Svetlana Nikic, Maarten IJzerman, Isabelle Durand Zaleski, Geert Frederix, Lars-Åke Levin, Charles G Mullighan, Reinhard Buttner, Trevor J Pugh, Sean M Grimmond, Carlos Caldas, Fabrice Andre, Ilse Custers, Elias Campo, Hans van Snellenberg, Anna Schuh, Hidewaki Nakagawa, Christof von Kalle, Torsten Haferlach, Stefan Fröhling, Vaidehi Jobanputra
Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care. JCO precision oncology 6 (2022)
Edwin Cuppen, Olivier Elemento, Richard Rosenquist, Svetlana Nikic, Maarten IJzerman, Isabelle Durand Zaleski, Geert Frederix, Lars-Åke Levin, Charles G Mullighan, Reinhard Buttner, Trevor J Pugh, Sean M Grimmond, Carlos Caldas, Fabrice Andre, Ilse Custers, Elias Campo, Hans van Snellenberg, Anna Schuh, Hidewaki Nakagawa, Christof von Kalle, Torsten Haferlach, Stefan Fröhling, Vaidehi Jobanputra
Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care. JCO precision oncology 6 (2022)
Mythily Ganapathi, Christie M Buchovecky, Fernando Cristo, Priyanka Ahimaz, Carrie Ruzal-Shapiro, Karen Wou, José M Inácio, Alejandro Iglesias, José A Belo, Vaidehi Jobanputra
A Novel Biallelic Loss-of-Function Variant in DAND5 Causes Heterotaxy Syndrome. Cold Spring Harbor molecular case studies (2022)
Christina A Austin-Tse, Vaidehi Jobanputra, Denise L Perry, David Bick, Ryan J Taft, Eric Venner, Richard A Gibbs, Edwin J Young, Sarah Barnett, John W Belmont, Nicole Boczek, Shimul Chowdhury, Katarzyna A Ellsworth, Saurav Guha, Shashikant Kulkarni, Cherisse Marcou, Linyan Meng, David R Murdock, Atteeq U Rehman, Elizabeth Spiteri, Amanda Thomas-Wilson, Hutton M Kearney, Heidi L Rehm, null null
Best practices for the interpretation and reporting of clinical whole genome sequencing. NPJ genomic medicine 7 (1) (2022)
Edwin Cuppen, Olivier Elemento, Richard Rosenquist, Svetlana Nikic, Maarten IJzerman, Isabelle Durand Zaleski, Geert Frederix, Lars-Åke Levin, Charles G Mullighan, Reinhard Buttner, Trevor J Pugh, Sean M Grimmond, Carlos Caldas, Fabrice Andre, Ilse Custers, Elias Campo, Hans van Snellenberg, Anna Schuh, Hidewaki Nakagawa, Christof von Kalle, Torsten Haferlach, Stefan Fröhling, Vaidehi Jobanputra
Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care. JCO precision oncology 6 (2022)
Edwin Cuppen, Olivier Elemento, Richard Rosenquist, Svetlana Nikic, Maarten IJzerman, Isabelle Durand Zaleski, Geert Frederix, Lars-Åke Levin, Charles G Mullighan, Reinhard Buttner, Trevor J Pugh, Sean M Grimmond, Carlos Caldas, Fabrice Andre, Ilse Custers, Elias Campo, Hans van Snellenberg, Anna Schuh, Hidewaki Nakagawa, Christof von Kalle, Torsten Haferlach, Stefan Fröhling, Vaidehi Jobanputra
Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care. JCO precision oncology 6 (2022)
Christian R Marshall, Shimul Chowdhury, Ryan J Taft, Matthew S Lebo, Jillian G Buchan, Steven M Harrison, Ross Rowsey, Eric W Klee, Pengfei Liu, Elizabeth A Worthey, Vaidehi Jobanputra, David P Dimmock, Hutton M Kearney, David Bick, Shashikant Kulkarni, Stacie L Taylor, John W Belmont, Dimitri J Stavropoulos, Niall J Lennon, null null
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease. NPJ genomic medicine 5 (2020)
Robin Z Hayeems, David P Dimmock, David Bick, John W Belmont, Robert C Green, Brendan Lanpher, Vaidehi Jobanputra, Roberto Mendoza-Londono, Shashi Kulkarni, Megan E Grove, Stacie L Taylor, Euan Ashley, null null
Clinical utility of genomic sequencing: a measurement toolkit. NPJ genomic medicine 5 (1) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Vaidehi Jobanputra