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Gary M Shaw

Showing results (501-510 of 530) with videos related to

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Birth Defects Research|July 11, 2024
Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention StudyElizabeth E Blue, Kristin J Moore, Kari E North, et al.
Nature|April 8, 2026
Single-cell spatiotemporal dissection of the human maternal-fetal interfaceCheng Wang, Yan Zhou, Yuejun Wang, et al.
AJOG Global Reports|July 17, 2023
Comparative predictive power of serum vs plasma proteomic signatures in feto-maternal medicineCamilo Espinosa, Said Mohammed Ali, Waqasuddin Khan, et al.
Birth Defects Research|March 11, 2022
Exome sequencing identifies variants in infants with sacral agenesisGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
Science Translational Medicine|January 21, 2026
Quantitative assessment of neonatal health using dried blood spot metabolite profiles and deep learningAlan L Chang, Jonathan D Reiss, Anthony Culos, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Single-cell-level digital twins for preterm birth prevention strategiesJakob Einhaus, Peter Neidlinger, Olivier Fondeur, et al.
Science Immunology|September 3, 2017
An immune clock of human pregnancyNima Aghaeepour, Edward A Ganio, David Mcilwain, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Rare variants in <i>PRKCI</i> cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Human Molecular Genetics|January 29, 2019
The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulationYoussef A Kousa, Huiping Zhu, Walid D Fakhouri, et al.
HGG Advances|September 4, 2023
Rare variants in <i>CAPN2</i> increase risk for isolated hypoplastic left heart syndromeElizabeth E Blue, Janson J White, Michael K Dush, et al.
Pageof 53

Showing results (501-510 of 530) with videos related to

Sort By:
Pageof 53
Birth Defects Research|July 11, 2024
Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention StudyElizabeth E Blue, Kristin J Moore, Kari E North, et al.
Nature|April 8, 2026
Single-cell spatiotemporal dissection of the human maternal-fetal interfaceCheng Wang, Yan Zhou, Yuejun Wang, et al.
AJOG Global Reports|July 17, 2023
Comparative predictive power of serum vs plasma proteomic signatures in feto-maternal medicineCamilo Espinosa, Said Mohammed Ali, Waqasuddin Khan, et al.
Birth Defects Research|March 11, 2022
Exome sequencing identifies variants in infants with sacral agenesisGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
Science Translational Medicine|January 21, 2026
Quantitative assessment of neonatal health using dried blood spot metabolite profiles and deep learningAlan L Chang, Jonathan D Reiss, Anthony Culos, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Single-cell-level digital twins for preterm birth prevention strategiesJakob Einhaus, Peter Neidlinger, Olivier Fondeur, et al.
Science Immunology|September 3, 2017
An immune clock of human pregnancyNima Aghaeepour, Edward A Ganio, David Mcilwain, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Rare variants in <i>PRKCI</i> cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Human Molecular Genetics|January 29, 2019
The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulationYoussef A Kousa, Huiping Zhu, Walid D Fakhouri, et al.
HGG Advances|September 4, 2023
Rare variants in <i>CAPN2</i> increase risk for isolated hypoplastic left heart syndromeElizabeth E Blue, Janson J White, Michael K Dush, et al.
Pageof 53