ScholarIQanswers from OpenAlex & ORCID
Terri H. Beaty
ResearcherPublications, citations & collaboration network
Terri H. Beaty is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Terri H. Beaty have?
ScholarIQindexed works
Terri H. Beaty has 583 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Terri H. Beaty have?
ScholarIQcitation count
Terri H. Beaty has 39,433 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Terri H. Beaty?
ScholarIQh-index
Terri H. Beaty has an h-index of 97 in OpenAlex.
What is the i10-index of Terri H. Beaty?
ScholarIQi10-index
Terri H. Beaty has an i10-index of 346 in OpenAlex.
What is the ORCID of Terri H. Beaty?
ScholarIQorcid
The ORCID for Terri H. Beaty is on the source record.
What is the OpenAlex record for Terri H. Beaty?
ScholarIQopenalex
The OpenAlex for Terri H. Beaty is on the source record.
What are the most-cited papers on Terri H. Beaty?
ScholarIQmost cited works
Tight junction defects in patients with atopic dermatitis
Anna De Benedetto, Nicholas Rafaels, Laura Y. McGirt, Andrei I. Ivanov, Steve N. Georas, Chris Cheadle, Alan E. Berger, Kunzhong Zhang, Sadasivan Vidyasagar, Takeshi Yoshida, Mark Boguniewicz, Tissa Hata, Lynda C. Schneider, Jon M. Hanifin, Richard L. Gallo, Natalija Novak, Stephan Weidinger, Terri H. Beaty, Donald Y.M. Leung, Kathleen C. Barnes, Lisa A. Beck
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Florence Démenais, Patricia Margaritte‐Jeannin, Kathleen C. Barnes, William Cookson, Janine Altmüller, Wei Ang, R. Graham Barr, Terri H. Beaty, Allan B. Becker, John Beilby, Hans Bisgaard, Unnur Steina Björnsdóttir, Eugene R. Bleecker, Klaus Bønnelykke, Dorret I. Boomsma, Emmanuelle Bouzigon, Christopher E. Brightling, Myriam Brossard, Guy Brusselle, Esteban G. Burchard, Kristin M. Burkart, Andrew Bush, Moira Chan‐Yeung, Kian Fan Chung, Alexessander Couto Alves, John A. Curtin, Adnan Čustović, Denise Daley, Johan C. de Jongste, Blanca E. Del-Río-Navarro, Kathleen Donohue, Liesbeth Duijts, Celeste Eng, Johan G. Eriksson, Martin Farrall, Yu. Yu. Fedorova, Bjarke Feenstra, Manuel A. R. Ferreira, Maxim B. Freidin, Zofia K. Z. Gajdos, Jim Gauderman, Ulrike Gehring, Frank Geller, Jon Genuneit, Sina A. Gharib, Frank D. Gilliland, Raquel Granell, Penelope E. Graves, Daníel F. Guðbjartsson, Tari Haahtela, Susan R. Heckbert, Dick Heederik, Joachim Heinrich, Markku Heliövaara, John Henderson, Blanca E. Himes, Hiroshi Hirose, Joel N. Hirschhorn, Albert Hofman, Patrick G. Holt, Jouke Hottenga, Thomas J. Hudson, Jennie Hui, Medea Imboden, В. П. Иванов, Vincent W. V. Jaddoe, Alan James, Christer Janson, Marjo‐Riitta Järvelin, Deborah Jarvis, Graham Jones, Ingileif Jónsdóttir, Jousilahti P, Michael Kabesch, Mika Kähönen, David B. Kantor, А. С. Карунас, Э. К. Хуснутдинова, Gerard H. Koppelman, Anita L. Kozyrskyj, Eskil Kreiner, Michiaki Kubo, Rajesh Kumar, Ashish Kumar, Mikko Kuokkanen, Lies Lahousse, Tarja Laitinen, Catherine Laprise, Mark Lathrop, Susanne Lau, Youngae Lee, Terho Lehtimäki, Sébastien Letort, Albert M. Levin, Li Guo, Liming Liang, Laura R. Loehr, Stephanie J. London, Daan W. Loth, Ani Manichaikul
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
Terri H. Beaty, Jeffrey C. Murray, Mary L. Marazita, Ronald G. Munger, Ingo Ruczinski, Jacqueline B. Hetmanski, Kung Yee Liang, Tao Wu, Tanda Murray, M. Daniele Fallin, Richard Redett, Gerald V. Raymond, Holger Schwender, Sheng Chih Jin, Margaret E. Cooper, Martine Dunnwald, M. Adela Mansilla, Elizabeth J. Leslie, Stephen Bullard, Andrew C. Lidral, Lina M. Moreno, Renato Menezes, Alexandre R. Vieira, Aline Petrin, Allen J. Wilcox, Rolv T. Lie, Ethylin Wang Jabs, Yah Huei Wu‐Chou, Philip K. Chen, Hong Wang, Xiaoqian Ye, Shangzhi Huang, Vincent Yeow, Samuel S. Chong, Sun Ha Jee, Bing Shi, Kaare Christensen, Mads Melbye, Kimberly F. Doheny, Elizabeth Pugh, Hua Ling, Eduardo E. Castilla, Andrew E. Czeizel, Lian Ma, L. Leigh Field, Lawrence C. Brody, Faith Pangilinan, James L. Mills, Anne M. Molloy, Peadar N. Kirke, John M. Scott, Mauricio Arcos‐Burgos, Alan F. Scott
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
Pierrick Wainschtein, Deepti Jain, Zhili Zheng, TOPMed Anthropometry Working Group, Stella Aslibekyan, Diane M. Becker, Wenjian Bi, Jennifer A. Brody, Jenna C. Carlson, Adolfo Correa, Margaret Mengmeng Du, Lindsay Fernández‐Rhodes, Kendra Ferrier, Misa Graff, Xiuqing Guo, Jiang He, Nancy L. Heard‐Costa, Heather M. Highland, Joel N. Hirschhorn, Candace M Howard-Claudio, Carmen R. Isasi, Rebecca D. Jackson, Jicai Jiang, Roby Joehanes, Anne E. Justice, Rita R. Kalyani, Sharon L. R. Kardia, Ethan M. Lange, Meryl S. LeBoff, Seunggeun Lee, Xihao Li, Zilin Li, Elise Lim, D. Y. Lin, Xihong Lin, Simin Liu, Yingchang Lu, JoAnn E. Manson, Lisa W. Martin, Caitlin McHugh, Julie Mikulla, Solomon K. Musani, Maggie Ng, Deborah A. Nickerson, Nicholette Palmer, James A. Perry, Ulrike Peters, Michael Preuß, Qibin Qi, Laura M. Raffield, Laura J. Rasmussen‐Torvik, Alex P. Reiner, Emily M. Russell, Colleen M. Sitlani, Jennifer A. Smith, Cassandra N. Spracklen, Tao Wang, Zhe Wang, Jennifer Wessel, Hanfei Xu, Mohammad Yaser, Sachiko Yoneyama, Kendra A. Young, Jingwen Zhang, Xinruo Zhang, Hufeng Zhou, Xiaofeng Zhu, Sebastian Zoellner, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis
Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children
Xiumei Hong, Ke Hao, Christine Ladd‐Acosta, Kasper D. Hansen, Hui‐Ju Tsai, Xin Liu, Xin Xu, Timothy A. Thornton, Deanna Caruso, Corinne Keet, Yifei Sun, Guoying Wang, Wei Luo, Rajesh Kumar, Ramsay Fuleihan, Anne Marie Singh, Jennifer S. Kim, Rachel E. Story, Ruchi S. Gupta, Peisong Gao, Zhu Chen, Sheila O. Walker, Tami R. Bartell, Terri H. Beaty, M. Daniele Fallin, Robert P. Schleimer, Patrick G. Holt, Kari C. Nadeau, Robert A. Wood, Jacqueline A. Pongracic, Daniel E. Weeks, Xiaobin Wang