Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting

por Liu, Huan, Leslie, Elizabeth J., Carlson, Jenna C., Beaty, Terri H., Marazita, Mary L., Lidral, Andrew C., Cornell, Robert A.
Publicado 2017

Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2

por Lee, Myoung Keun, Shaffer, John R., Leslie, Elizabeth J., Orlova, Ekaterina, Carlson, Jenna C., Feingold, Eleanor, Marazita, Mary L., Weinberg, Seth M.
Publicado 2017

Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay

por Duverger, Olivier, Carlson, Jenna C., Karacz, Chelsea M., Schwartz, Mary E., Cross, Michael A., Marazita, Mary L., Shaffer, John R., Morasso, Maria I.
Publicado 2018

Correction: Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay

por Duverger, Olivier, Carlson, Jenna C., Karacz, Chelsea M., Schwartz, Mary E., Cross, Michael A., Marazita, Mary L., Shaffer, John R., Morasso, Maria I.
Publicado 2019

Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk

por Carlson, Jenna C., Shaffer, John R., Deleyiannis, Fred, Hecht, Jacqueline T., Wehby, George L., Christensen, Kaare, Feingold, Eleanor, Weinberg, Seth M., Marazita, Mary L., Leslie, Elizabeth J.
Publicado 2022

Correlates of daytime sleepiness and insomnia among adults in Samoa

por Heinsberg, Lacey W., Carlson, Jenna C., Pomer, Alysa, Cade, Brian E., Naseri, Take, Reupena, Muagututia Sefuiva, Weeks, Daniel E., McGarvey, Stephen T., Redline, Susan, Hawley, Nicola L.
Publicado 2022

Rare genetic variants in SEC24D modify orofacial cleft phenotypes

por Curtis, Sarah W., Carlson, Jenna C., Beaty, Terri H., Murray, Jeffrey C., Weinberg, Seth M., Marazita, Mary L., Cotney, Justin L., Cutler, David J., Epstein, Michael P., Leslie, Elizabeth J.
Publicado 2023

The missense variant, rs373863828, in CREBRF plays a role in longitudinal changes in body mass index in Samoans

por Fu, Haoyi, Hawley, Nicola L., Carlson, Jenna C., Russell, Emily M., Pomer, Alysa, Cheng, Hong, Naseri, Take, Reupena, Muagututi’a Sefuiva, Deka, Ranjan, Choy, Courtney C., McGarvey, Stephen T., Minster, Ryan L., Weeks, Daniel E.
Publicado 2022

The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip

por Curtis, Sarah W., Chang, Daniel, Lee, Myoung Keun, Shaffer, John R., Indencleef, Karlijne, Epstein, Michael P., Cutler, David J., Murray, Jeffrey C., Feingold, Eleanor, Beaty, Terri H., Claes, Peter, Weinberg, Seth M., Marazita, Mary L., Carlson, Jenna C., Leslie, Elizabeth J.
Publicado 2021

Protocol: Implementation and evaluation of an adolescent-mediated intervention to improve glycemic control and diabetes self-management among Samoan adults

por Hawley, Nicola L., Rivara, Anna C., Naseri, Joshua, Faumuina, Kitiona, Potoa’e-Solaita, Noelle, Iopu, Francine, Faiai, Mata’uitafa, Naveno, Eminoni, Tasele, Susie, Lefale, Temukisa, Lantini, Ryan, Carlson, Jenna C., Rabin, Tracy L., Semaia, Penny, Mugadza, Phyllis, Rosen, Rochelle K.
Publicado 2023

CREBRF missense variant rs373863828 has both direct and indirect effects on type 2 diabetes and fasting glucose in Polynesian peoples living in Samoa and Aotearoa New Zealand

por Russell, Emily M, Carlson, Jenna C, Krishnan, Mohanraj, Hawley, Nicola L, Sun, Guangyun, Cheng, Hong, Naseri, Take, Reupena, Muagututi‘a Sefuiva, Viali, Satupa‘itea, Tuitele, John, Major, Tanya J, Miljkovic, Iva, Merriman, Tony R, Deka, Ranjan, Weeks, Daniel E, McGarvey, Stephen T, Minster, Ryan L
Publicado 2022

Exploring the genomic basis of early childhood caries: a pilot study

por Ballantine, Jami L., Carlson, Jenna C., Ferreira Zandoná, Andrea G., Agler, Cary, Zeldin, Leslie P., Rozier, Richard Gary, Roberts, Michael W., Basta, Patricia V., Luo, Jason, Antonio‐Obese, Mikafui E., McNeil, Daniel W., Weyant, Robert J., Crout, Richard J., Slayton, Rebecca L., Levy, Steven M., Shaffer, John R., Marazita, Mary L., North, Kari E., Divaris, Kimon
Publicado 2017

A stop-gain variant in BTNL9 is associated with atherogenic lipid profiles

por Carlson, Jenna C., Krishnan, Mohanraj, Rosenthal, Samantha L., Russell, Emily M., Zhang, Jerry Z., Hawley, Nicola L., Moors, Jaye, Cheng, Hong, Dalbeth, Nicola, de Zoysa, Janak R., Watson, Huti, Qasim, Muhammad, Murphy, Rinki, Naseri, Take, Reupena, Muagututi’a Sefuiva, Viali, Satupa‘itea, Stamp, Lisa K., Tuitele, John, Kershaw, Erin E., Deka, Ranjan, McGarvey, Stephen T., Merriman, Tony R., Weeks, Daniel E., Minster, Ryan L.
Publicado 2022

Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment

por Shaffer, John R., Li, Jinxi, Lee, Myoung Keun, Roosenboom, Jasmien, Orlova, Ekaterina, Adhikari, Kaustabh, Gallo, Carla, Poletti, Giovanni, Schuler-Faccini, Lavinia, Bortolini, Maria-Cátira, Canizales-Quinteros, Samuel, Rothhammer, Francisco, Bedoya, Gabriel, González-José, Rolando, Pfeffer, Paige E., Wollenschlaeger, Christopher A., Hecht, Jacqueline T., Wehby, George L., Moreno, Lina M., Ding, Anan, Jin, Li, Yang, Yajun, Carlson, Jenna C., Leslie, Elizabeth J., Feingold, Eleanor, Marazita, Mary L., Hinds, David A., Cox, Timothy C., Wang, Sijia, Ruiz-Linares, Andrés, Weinberg, Seth M.
Publicado 2017

Exploring the Paradoxical Relationship of a Creb 3 Regulatory Factor Missense Variant With Body Mass Index and Diabetes Among Samoans: Protocol for the Soifua Manuia (Good Health)...

por Hawley, Nicola L, Pomer, Alysa, Rivara, Anna C., Rosenthal, Samantha L, Duckham, Rachel L, Carlson, Jenna C, Naseri, Take, Reupena, Muagututia Sefuiva, Selu, Melania, Lupematisila, Vaimoana, Unasa, Folla, Vesi, Lupesina, Fatu, Tracy, Unasa, Seipepa, Faasalele-Savusa, Kima, Wetzel, Abigail I, Soti-Ulberg, Christina, Prescott, Angela T, Siufaga, Gloria, Penaia, Corina, To, Sophie B., LaMonica, Lauren C, Lameko, Viali, Choy, Courtney C, Crouter, Scott E, Redline, Susan, Deka, Ranjan, Kershaw, Erin E, Urban, Zsolt, Minster, Ryan L., Weeks, Daniel E., McGarvey, Stephen T
Publicado 2020

A Polynesian-specific missense CETP variant alters the lipid profile

por Moors, Jaye, Krishnan, Mohanraj, Sumpter, Nick, Takei, Riku, Bixley, Matt, Cadzow, Murray, Major, Tanya J., Phipps-Green, Amanda, Topless, Ruth, Merriman, Marilyn, Rutledge, Malcolm, Morgan, Ben, Carlson, Jenna C., Zhang, Jerry Z., Russell, Emily M., Sun, Guangyun, Cheng, Hong, Weeks, Daniel E., Naseri, Take, Reupena, Muagututi’a Sefuiva, Viali, Satupa’itea, Tuitele, John, Hawley, Nicola L., Deka, Ranjan, McGarvey, Stephen T., de Zoysa, Janak, Murphy, Rinki, Dalbeth, Nicola, Stamp, Lisa, Taumoepeau, Mele, King, Frances, Wilcox, Phillip, Rapana, Nuku, McCormick, Sally, Minster, Ryan L., Merriman, Tony R., Leask, Megan
Publicado 2023

A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies

por Li, Xihao, Chen, Han, Selvaraj, Margaret Sunitha, Van Buren, Eric, Zhou, Hufeng, Wang, Yuxuan, Sun, Ryan, McCaw, Zachary R., Yu, Zhi, Arnett, Donna K., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Brody, Jennifer A., Cade, Brian E., Carson, April P., Carlson, Jenna C., Chami, Nathalie, Chen, Yii-Der Ida, Curran, Joanne E., de Vries, Paul S., Fornage, Myriam, Franceschini, Nora, Freedman, Barry I., Gu, Charles, Heard-Costa, Nancy L., He, Jiang, Hou, Lifang, Hung, Yi-Jen, Irvin, Marguerite R., Kaplan, Robert C., Kardia, Sharon L.R., Kelly, Tanika, Konigsberg, Iain, Kooperberg, Charles, Kral, Brian G., Li, Changwei, Loos, Ruth J.F., Mahaney, Michael C., Martin, Lisa W., Mathias, Rasika A., Minster, Ryan L., Mitchell, Braxton D., Montasser, May E., Morrison, Alanna C., Palmer, Nicholette D., Peyser, Patricia A., Psaty, Bruce M., Raffield, Laura M., Redline, Susan, Reiner, Alexander P., Rich, Stephen S., Sitlani, Colleen M., Smith, Jennifer A., Taylor, Kent D., Tiwari, Hemant, Vasan, Ramachandran S., Wang, Zhe, Yanek, Lisa R., Yu, Bing, Rice, Kenneth M., Rotter, Jerome I., Peloso, Gina M., Natarajan, Pradeep, Li, Zilin, Liu, Zhonghua, Lin, Xihong
Publicado 2023

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study

por Wang, Yuxuan, Selvaraj, Margaret Sunitha, Li, Xihao, Li, Zilin, Holdcraft, Jacob A., Arnett, Donna K., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Cade, Brian E., Carlson, Jenna C., Carson, April P., Chen, Yii-Der Ida, Curran, Joanne E., de Vries, Paul S., Dutcher, Susan K., Ellinor, Patrick T., Floyd, James S., Fornage, Myriam, Freedman, Barry I., Gabriel, Stacey, Germer, Soren, Gibbs, Richard A., Guo, Xiuqing, He, Jiang, Heard-Costa, Nancy, Hildalgo, Bertha, Hou, Lifang, Irvin, Marguerite R., Joehanes, Roby, Kaplan, Robert C., Kardia, Sharon LR., Kelly, Tanika N., Kim, Ryan, Kooperberg, Charles, Kral, Brian G., Levy, Daniel, Li, Changwei, Liu, Chunyu, Lloyd-Jone, Don, Loos, Ruth JF., Mahaney, Michael C., Martin, Lisa W., Mathias, Rasika A., Minster, Ryan L., Mitchell, Braxton D., Montasser, May E., Morrison, Alanna C., Murabito, Joanne M., Naseri, Take, O’Connell, Jeffrey R., Palmer, Nicholette D., Preuss, Michael H., Psaty, Bruce M., Raffield, Laura M., Rao, Dabeeru C., Redline, Susan, Reiner, Alexander P., Rich, Stephen S., Ruepena, Muagututi’a Sefuiva, Sheu, Wayne H-H., Smith, Jennifer A., Smith, Albert, Tiwari, Hemant K., Tsai, Michael Y., Viaud-Martinez, Karine A., Wang, Zhe, Yanek, Lisa R., Zhao, Wei, Rotter, Jerome I., Lin, Xihong, Natarajan, Pradeep, Peloso, Gina M.
Publicado 2023