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Birth Defects Research
|
April 30, 2025
Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention Study
Tonia C Carter, Denise M Kay, Faith Pangilinan, et al.
American Journal of Human Genetics
|
September 3, 2025
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy
Kelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Scientific Reports
|
January 11, 2018
A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth
Nadav Rappoport, Jonathan Toung, Dexter Hadley, et al.
American Journal of Medical Genetics. Part A
|
March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants
Pagna Sok, Aniko Sabo, Lynn M Almli, et al.
Science Translational Medicine
|
May 6, 2021
Integrated trajectories of the maternal metabolome, proteome, and immunome predict labor onset
Ina A Stelzer, Mohammad S Ghaemi, Xiaoyuan Han, et al.
Bioinformatics (Oxford, England)
|
December 19, 2018
Multiomics modeling of the immunome, transcriptome, microbiome, proteome and metabolome adaptations during human pregnancy
Mohammad Sajjad Ghaemi, Daniel B DiGiulio, Kévin Contrepois, et al.
Nature Medicine
|
March 26, 2025
AI-guided precision parenteral nutrition for neonatal intensive care units
Thanaphong Phongpreecha, Marc Ghanem, Jonathan D Reiss, et al.
Science Advances
|
May 24, 2023
Multiomic signals associated with maternal epidemiological factors contributing to preterm birth in low- and middle-income countries
Camilo A Espinosa, Waqasuddin Khan, Rasheda Khanam, et al.
JAMA Network Open
|
December 18, 2020
Multiomics Characterization of Preterm Birth in Low- and Middle-Income Countries
Fyezah Jehan, Sunil Sazawal, Abdullah H Baqui, et al.
Genetics in Medicine Open
|
September 30, 2024
Regulatory elements in <i>SEM1-DLX5-DLX6</i> (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits
Paola Nicoletti, Samreen Zafer, Lital Matok, et al.
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Search research articles
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Showing results (521-530 of 530) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 530 results.
Birth Defects Research
|
April 30, 2025
Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention Study
Tonia C Carter, Denise M Kay, Faith Pangilinan, et al.
American Journal of Human Genetics
|
September 3, 2025
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy
Kelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Scientific Reports
|
January 11, 2018
A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth
Nadav Rappoport, Jonathan Toung, Dexter Hadley, et al.
American Journal of Medical Genetics. Part A
|
March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants
Pagna Sok, Aniko Sabo, Lynn M Almli, et al.
Science Translational Medicine
|
May 6, 2021
Integrated trajectories of the maternal metabolome, proteome, and immunome predict labor onset
Ina A Stelzer, Mohammad S Ghaemi, Xiaoyuan Han, et al.
Bioinformatics (Oxford, England)
|
December 19, 2018
Multiomics modeling of the immunome, transcriptome, microbiome, proteome and metabolome adaptations during human pregnancy
Mohammad Sajjad Ghaemi, Daniel B DiGiulio, Kévin Contrepois, et al.
Nature Medicine
|
March 26, 2025
AI-guided precision parenteral nutrition for neonatal intensive care units
Thanaphong Phongpreecha, Marc Ghanem, Jonathan D Reiss, et al.
Science Advances
|
May 24, 2023
Multiomic signals associated with maternal epidemiological factors contributing to preterm birth in low- and middle-income countries
Camilo A Espinosa, Waqasuddin Khan, Rasheda Khanam, et al.
JAMA Network Open
|
December 18, 2020
Multiomics Characterization of Preterm Birth in Low- and Middle-Income Countries
Fyezah Jehan, Sunil Sazawal, Abdullah H Baqui, et al.
Genetics in Medicine Open
|
September 30, 2024
Regulatory elements in <i>SEM1-DLX5-DLX6</i> (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits
Paola Nicoletti, Samreen Zafer, Lital Matok, et al.
Page
of 53