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W Curtis

Showing results (201-210 of 218) with videos related to

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Environmental Health : a Global Access Science Source|August 25, 2019
Thyroid hormone levels associate with exposure to polychlorinated biphenyls and polybrominated biphenyls in adults exposed as childrenSarah W Curtis, Metrecia L Terrell, Melanie H Jacobson, et al.
HGG Advances|April 5, 2021
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lipSarah W Curtis, Daniel Chang, Myoung Keun Lee, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2025
Identification of functional non-coding variants associated with orofacial cleftPriyanka Kumari, Ryan Z Friedman, Lira Pi, et al.
Nature Communications|July 16, 2025
Identification of functional non-coding variants associated with orofacial cleftPriyanka Kumari, Ryan Z Friedman, Sarah W Curtis, et al.
Biorxiv : the Preprint Server for Biology|July 15, 2024
Functional analysis of <i>ESRP1/2</i> gene variants and <i>CTNND1</i> isoforms in orofacial cleft pathogenesisCaroline Caetano da Silva, Claudio Macias Trevino, Jason Mitchell, et al.
Communications Biology|August 23, 2024
Functional analysis of ESRP1/2 gene variants and CTNND1 isoforms in orofacial cleft pathogenesisCaroline Caetano da Silva, Claudio Macias Trevino, Jason Mitchell, et al.
Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Human Molecular Genetics|October 31, 2025
Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.
American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Pageof 22

Showing results (201-210 of 218) with videos related to

Sort By:
Pageof 22
Environmental Health : a Global Access Science Source|August 25, 2019
Thyroid hormone levels associate with exposure to polychlorinated biphenyls and polybrominated biphenyls in adults exposed as childrenSarah W Curtis, Metrecia L Terrell, Melanie H Jacobson, et al.
HGG Advances|April 5, 2021
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lipSarah W Curtis, Daniel Chang, Myoung Keun Lee, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2025
Identification of functional non-coding variants associated with orofacial cleftPriyanka Kumari, Ryan Z Friedman, Lira Pi, et al.
Nature Communications|July 16, 2025
Identification of functional non-coding variants associated with orofacial cleftPriyanka Kumari, Ryan Z Friedman, Sarah W Curtis, et al.
Biorxiv : the Preprint Server for Biology|July 15, 2024
Functional analysis of <i>ESRP1/2</i> gene variants and <i>CTNND1</i> isoforms in orofacial cleft pathogenesisCaroline Caetano da Silva, Claudio Macias Trevino, Jason Mitchell, et al.
Communications Biology|August 23, 2024
Functional analysis of ESRP1/2 gene variants and CTNND1 isoforms in orofacial cleft pathogenesisCaroline Caetano da Silva, Claudio Macias Trevino, Jason Mitchell, et al.
Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Human Molecular Genetics|October 31, 2025
Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.
American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Pageof 22