Patricia K Donahoe

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 9

Top Topics

Transcription Factor

Regulatory T Cells

Congenital Heart Disease

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

Journal of pediatric genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Katherine E Pendleton, Andres Hernandez-Garcia, Jennifer M Lyu, Ian M Campbell, Chad A Shaw, Julie Vogt, Frances A High, Patricia K Donahoe, Wendy K Chung, Daryl A Scott
FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia. Journal of pediatric genetics 13 (1) (2023)
Katherine E Pendleton, Andres Hernandez-Garcia, Jennifer M Lyu, Ian M Campbell, Chad A Shaw, Julie Vogt, Frances A High, Patricia K Donahoe, Wendy K Chung, Daryl A Scott
FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia. Journal of pediatric genetics 13 (1) (2023)
Katherine E Pendleton, Andres Hernandez-Garcia, Jennifer M Lyu, Ian M Campbell, Chad A Shaw, Julie Vogt, Frances A High, Patricia K Donahoe, Wendy K Chung, Daryl A Scott
FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia. Journal of pediatric genetics 13 (1) (2023)
Katherine E Pendleton, Andres Hernandez-Garcia, Jennifer M Lyu, Ian M Campbell, Chad A Shaw, Julie Vogt, Frances A High, Patricia K Donahoe, Wendy K Chung, Daryl A Scott
FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia. Journal of pediatric genetics 13 (1) (2023)
Yi Li, Lina Wei, Marie-Charlotte Meinsohn, Rana Suliman, Maeva Chauvin, Jim Berstler, Kate Hartland, Mark M Jensen, Natalie A Sicher, Nicholas Nagykery, Patricia K Donahoe, David Pépin
A screen of repurposed drugs identifies AMHR2/MISR2 agonists as potential contraceptives. Proceedings of the National Academy of Sciences of the United States of America 119 (15) (2022)
Marie-Charlotte Meinsohn, Hatice Duygu Saatcioglu, Lina Wei, Yi Li, Heiko Horn, Maeva Chauvin, Motohiro Kano, Ngoc Minh Phuong Nguyen, Nicholas Nagykery, Aki Kashiwagi, Wesley R Samore, Dan Wang, Esther Oliva, Guangping Gao, Mary E Morris, Patricia K Donahoe, David Pépin
Single-cell sequencing reveals suppressive transcriptional programs regulated by MIS/AMH in neonatal ovaries. Proceedings of the National Academy of Sciences of the United States of America 118 (20) (2021)
Kaitlin N Hart, William A Stocker, Nicholas G Nagykery, Kelly L Walton, Craig A Harrison, Patricia K Donahoe, David Pépin, Thomas B Thompson
Structure of AMH bound to AMHR2 provides insight into a unique signaling pair in the TGF-β family. Proceedings of the National Academy of Sciences of the United States of America 118 (26) (2021)
Qihui Zhu, Frances A High, Chengsheng Zhang, Eliza Cerveira, Meaghan K Russell, Mauro Longoni, Maliackal P Joy, Mallory Ryan, Adam Mil-Homens, Lauren Bellfy, Caroline M Coletti, Pooja Bhayani, Regis Hila, Jay M Wilson, Patricia K Donahoe, Charles Lee
Systematic analysis of copy number variation associated with congenital diaphragmatic hernia. Proceedings of the National Academy of Sciences of the United States of America 115 (20) (2018)
Hongjian Qi, Lan Yu, Xueya Zhou, Julia Wynn, Haoquan Zhao, Yicheng Guo, Na Zhu, Alexander Kitaygorodsky, Rebecca Hernan, Gudrun Aspelund, Foong-Yen Lim, Timothy Crombleholme, Robert Cusick, Kenneth Azarow, Melissa E Danko, Dai Chung, Brad W Warner, George B Mychaliska, Douglas Potoka, Amy J Wagner, Mahmoud M Elfiky, Jay M Wilson, Debbie Nickerson, Michael J Bamshad, Frances A High, Mauro Longoni, Patricia K Donahoe, Wendy K Chung, Yufeng Shen
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders. PLoS genetics 14 (12) (2018)