Jonathan J Lyons (J J Lyons)

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 22

Top Topics

Atopic Dermatitis

Top Venues

The Journal of experimental medicine

Nature communications

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

Publications

Jeremy C McMurray, Curtis S Pacheco, Brandon J Schornack, Xiaoping Sun, Janet A Brunader, Alexis E Scott, Juan S Ariza, Chung-Ting J Kou, Ryan C Costantino, Luke M Pittman, Karla E Adams, Aubri M Waters, Eric M Pryor, Jonathan J Lyons, Dean D Metcalfe, Irina Maric, Nathan A Boggs
Standardized indolent systemic mastocytosis evaluations across a health care system: implications for screening accuracy. Blood 144 (4) (2024)
Brian Walitt, Komudi Singh, Samuel R LaMunion, Mark Hallett, Steve Jacobson, Kong Y Chen, Yoshimi Enose-Akahata, Richard Apps, Jennifer J Barb, Patrick Bedard, Robert J Brychta, Ashura Williams Buckley, Peter Denis Burbelo, Brice Calco, Brianna Cathay, Li Chen, Snigdha Chigurupati, Jinguo Chen, Foo Cheung, Lisa M K Chin, Benjamin W Coleman, Amber B Courville, Madeleine S Deming, Bart Drinkard, Li Rebekah Feng, Luigi Ferruci, Scott A Gabel, Angelique Gavin, David S Goldstein, Shahin Hassanzadeh, Sean C Horan, Silvina G Horovitz, Kory R Johnson, Anita Jones Govan, Kristine M Knutson, Joy D Kreskow, Mark D Levin, Jonathan J Lyons, Nicholas Madian, Nasir Malik, Andrew Lee Mammen, John A McCulloch, Patrick M McGurrin, Joshua D Milner, Ruin Moaddel, Geoffrey A Mueller, Amrita Mukherjee, Sandra Muñoz-Braceras, Gina Norato, Katherine Pak, Iago Pinal-Fernandez, Traian Popa, Lauren B Reoma, Michael N Sack, Farinaz Safavi, Leorey N Saligan, Brian A Sellers, Stephen Sinclair, Bryan Smith, Joseph Snow, Stacey Solin, Barbara J Stussman, Giorgio Trinchieri, Sara A Turner, C Stephenie Vetter, Felipe Vial, Carlotta Vizioli, Ashley Williams, Shanna B Yang, null null, Avindra Nath
Deep phenotyping of post-infectious myalgic encephalomyelitis/chronic fatigue syndrome. Nature communications 15 (1) (2024)
Jeremy C McMurray, Curtis S Pacheco, Brandon J Schornack, Xiaoping Sun, Janet A Brunader, Alexis E Scott, Juan S Ariza, Chung-Ting J Kou, Ryan C Costantino, Luke M Pittman, Karla E Adams, Aubri M Waters, Eric M Pryor, Jonathan J Lyons, Dean D Metcalfe, Irina Maric, Nathan A Boggs
Standardized indolent systemic mastocytosis evaluations across a health care system: implications for screening accuracy. Blood 144 (4) (2024)
Brian Walitt, Komudi Singh, Samuel R LaMunion, Mark Hallett, Steve Jacobson, Kong Y Chen, Yoshimi Enose-Akahata, Richard Apps, Jennifer J Barb, Patrick Bedard, Robert J Brychta, Ashura Williams Buckley, Peter Denis Burbelo, Brice Calco, Brianna Cathay, Li Chen, Snigdha Chigurupati, Jinguo Chen, Foo Cheung, Lisa M K Chin, Benjamin W Coleman, Amber B Courville, Madeleine S Deming, Bart Drinkard, Li Rebekah Feng, Luigi Ferruci, Scott A Gabel, Angelique Gavin, David S Goldstein, Shahin Hassanzadeh, Sean C Horan, Silvina G Horovitz, Kory R Johnson, Anita Jones Govan, Kristine M Knutson, Joy D Kreskow, Mark D Levin, Jonathan J Lyons, Nicholas Madian, Nasir Malik, Andrew Lee Mammen, John A McCulloch, Patrick M McGurrin, Joshua D Milner, Ruin Moaddel, Geoffrey A Mueller, Amrita Mukherjee, Sandra Muñoz-Braceras, Gina Norato, Katherine Pak, Iago Pinal-Fernandez, Traian Popa, Lauren B Reoma, Michael N Sack, Farinaz Safavi, Leorey N Saligan, Brian A Sellers, Stephen Sinclair, Bryan Smith, Joseph Snow, Stacey Solin, Barbara J Stussman, Giorgio Trinchieri, Sara A Turner, C Stephenie Vetter, Felipe Vial, Carlotta Vizioli, Ashley Williams, Shanna B Yang, null null, Avindra Nath
Deep phenotyping of post-infectious myalgic encephalomyelitis/chronic fatigue syndrome. Nature communications 15 (1) (2024)
Jeremy C McMurray, Curtis S Pacheco, Brandon J Schornack, Xiaoping Sun, Janet A Brunader, Alexis Erica Scott, Juan S Ariza, Chung-Ting J Kou, Ryan C Costantino, Luke M Pittman, Karla E Adams, Aubri M Waters, Eric M Pryor, Jonathan J Lyons, Dean Metcalfe, Irina Maric, Nathan A Boggs
Standardized indolent systemic mastocytosis evaluations across a healthcare system: implications for screening accuracy. Blood (2024)
Brian Walitt, Komudi Singh, Samuel R LaMunion, Mark Hallett, Steve Jacobson, Kong Y Chen, Yoshimi Enose-Akahata, Richard Apps, Jennifer J Barb, Patrick Bedard, Robert J Brychta, Ashura Williams Buckley, Peter Denis Burbelo, Brice Calco, Brianna Cathay, Li Chen, Snigdha Chigurupati, Jinguo Chen, Foo Cheung, Lisa M K Chin, Benjamin W Coleman, Amber B Courville, Madeleine S Deming, Bart Drinkard, Li Rebekah Feng, Luigi Ferruci, Scott A Gabel, Angelique Gavin, David S Goldstein, Shahin Hassanzadeh, Sean C Horan, Silvina G Horovitz, Kory R Johnson, Anita Jones Govan, Kristine M Knutson, Joy D Kreskow, Mark D Levin, Jonathan J Lyons, Nicholas Madian, Nasir Malik, Andrew Lee Mammen, John A McCulloch, Patrick M McGurrin, Joshua D Milner, Ruin Moaddel, Geoffrey A Mueller, Amrita Mukherjee, Sandra Muñoz-Braceras, Gina Norato, Katherine Pak, Iago Pinal-Fernandez, Traian Popa, Lauren B Reoma, Michael N Sack, Farinaz Safavi, Leorey N Saligan, Brian A Sellers, Stephen Sinclair, Bryan Smith, Joseph Snow, Stacey Solin, Barbara J Stussman, Giorgio Trinchieri, Sara A Turner, C Stephenie Vetter, Felipe Vial, Carlotta Vizioli, Ashley Williams, Shanna B Yang, null null, Avindra Nath
Deep phenotyping of post-infectious myalgic encephalomyelitis/chronic fatigue syndrome. Nature communications 15 (1) (2024)
Mehul Sharma, Daniel Leung, Mana Momenilandi, Lauren C W Jones, Lucia Pacillo, Alyssa E James, Jill R Murrell, Selket Delafontaine, Jesmeen Maimaris, Maryam Vaseghi-Shanjani, Kate L Del Bel, Henry Y Lu, Gilbert T Chua, Silvia Di Cesare, Oriol Fornes, Zhongyi Liu, Gigliola Di Matteo, Maggie P Fu, Donato Amodio, Issan Yee San Tam, Gavin Shueng Wai Chan, Ashish A Sharma, Joshua Dalmann, Robin van der Lee, Geraldine Blanchard-Rohner, Susan Lin, Quentin Philippot, Phillip Andrew Richmond, Jessica J Lee, Allison Matthews, Michael Seear, Alexandra K Turvey, Rachael L Philips, Terri F Brown-Whitehorn, Christopher J Gray, Kosuke Izumi, James R Treat, Kathleen H Wood, Justin Lack, Asya Khleborodova, Julie E Niemela, Xingtian Yang, Rui Liang, Lin Kui, Christina Sze-Man Wong, Grace Wing Kit Poon, Alexander Hoischen, Caspar I van der Made, Jing Yang, Koon Wing Chan, Jaime Sou Da Rosa Duque, Pamela Pui-Wah Lee, Marco Hok Kung Ho, Brian Hon-Yin Chung, Huong Thi Minh Le, Wanling Yang, Pejman Rohani, Ali Fouladvand, Hassan Rokni-Zadeh, Majid Changi-Ashtiani, Mohammad Miryounesi, Anne Puel, Mohammad Shahrooei, Andrea Finocchi, Paolo Rossi, Beatrice Rivalta, Cristina Cifaldi, Antonio Novelli, Chiara Passarelli, Stefania Arasi, Dominique M A Bullens, Kate Sauer, Tania Claeys, Catherine M Biggs, Emma Catherine Morris, Sergio D Rosenzweig, John J O'Shea, Wyeth W Wasserman, H Melanie Bedford, Clara D M van Karnebeek, Paolo Palma, Siobhan O Burns, Isabelle Meyts, Jean Laurent Casanova, Jonathan J Lyons, Nima Parvaneh, Anh Thi Van Nguyen, Caterina Cancrini, Jennifer Heimall, Hanan Ahmed, Margaret L McKinnon, Yu-Lung Lau, Vivien Béziat, Suzanne C Tough
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease. The Journal of experimental medicine 220 (5) (2023)
Mehul Sharma, Daniel Leung, Mana Momenilandi, Lauren C W Jones, Lucia Pacillo, Alyssa E James, Jill R Murrell, Selket Delafontaine, Jesmeen Maimaris, Maryam Vaseghi-Shanjani, Kate L Del Bel, Henry Y Lu, Gilbert T Chua, Silvia Di Cesare, Oriol Fornes, Zhongyi Liu, Gigliola Di Matteo, Maggie P Fu, Donato Amodio, Issan Yee San Tam, Gavin Shueng Wai Chan, Ashish A Sharma, Joshua Dalmann, Robin van der Lee, Geraldine Blanchard-Rohner, Susan Lin, Quentin Philippot, Phillip Andrew Richmond, Jessica J Lee, Allison Matthews, Michael Seear, Alexandra K Turvey, Rachael L Philips, Terri F Brown-Whitehorn, Christopher J Gray, Kosuke Izumi, James R Treat, Kathleen H Wood, Justin Lack, Asya Khleborodova, Julie E Niemela, Xingtian Yang, Rui Liang, Lin Kui, Christina Sze-Man Wong, Grace Wing Kit Poon, Alexander Hoischen, Caspar I van der Made, Jing Yang, Koon Wing Chan, Jaime Sou Da Rosa Duque, Pamela Pui-Wah Lee, Marco Hok Kung Ho, Brian Hon-Yin Chung, Huong Thi Minh Le, Wanling Yang, Pejman Rohani, Ali Fouladvand, Hassan Rokni-Zadeh, Majid Changi-Ashtiani, Mohammad Miryounesi, Anne Puel, Mohammad Shahrooei, Andrea Finocchi, Paolo Rossi, Beatrice Rivalta, Cristina Cifaldi, Antonio Novelli, Chiara Passarelli, Stefania Arasi, Dominique M A Bullens, Kate Sauer, Tania Claeys, Catherine M Biggs, Emma Catherine Morris, Sergio D Rosenzweig, John J O'Shea, Wyeth W Wasserman, H Melanie Bedford, Clara D M van Karnebeek, Paolo Palma, Siobhan O Burns, Isabelle Meyts, Jean Laurent Casanova, Jonathan J Lyons, Nima Parvaneh, Anh Thi Van Nguyen, Caterina Cancrini, Jennifer Heimall, Hanan Ahmed, Margaret L McKinnon, Yu-Lung Lau, Vivien Béziat, Suzanne C Tough
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease. The Journal of experimental medicine 220 (5) (2023)
Mehul Sharma, Daniel Leung, Mana Momenilandi, Lauren C W Jones, Lucia Pacillo, Alyssa E James, Jill R Murrell, Selket Delafontaine, Jesmeen Maimaris, Maryam Vaseghi-Shanjani, Kate L Del Bel, Henry Y Lu, Gilbert T Chua, Silvia Di Cesare, Oriol Fornes, Zhongyi Liu, Gigliola Di Matteo, Maggie P Fu, Donato Amodio, Issan Yee San Tam, Gavin Shueng Wai Chan, Ashish A Sharma, Joshua Dalmann, Robin van der Lee, Geraldine Blanchard-Rohner, Susan Lin, Quentin Philippot, Phillip Andrew Richmond, Jessica J Lee, Allison Matthews, Michael Seear, Alexandra K Turvey, Rachael L Philips, Terri F Brown-Whitehorn, Christopher J Gray, Kosuke Izumi, James R Treat, Kathleen H Wood, Justin Lack, Asya Khleborodova, Julie E Niemela, Xingtian Yang, Rui Liang, Lin Kui, Christina Sze-Man Wong, Grace Wing Kit Poon, Alexander Hoischen, Caspar I van der Made, Jing Yang, Koon Wing Chan, Jaime Sou Da Rosa Duque, Pamela Pui-Wah Lee, Marco Hok Kung Ho, Brian Hon-Yin Chung, Huong Thi Minh Le, Wanling Yang, Pejman Rohani, Ali Fouladvand, Hassan Rokni-Zadeh, Majid Changi-Ashtiani, Mohammad Miryounesi, Anne Puel, Mohammad Shahrooei, Andrea Finocchi, Paolo Rossi, Beatrice Rivalta, Cristina Cifaldi, Antonio Novelli, Chiara Passarelli, Stefania Arasi, Dominique M A Bullens, Kate Sauer, Tania Claeys, Catherine M Biggs, Emma Catherine Morris, Sergio D Rosenzweig, John J O'Shea, Wyeth W Wasserman, H Melanie Bedford, Clara D M van Karnebeek, Paolo Palma, Siobhan O Burns, Isabelle Meyts, Jean Laurent Casanova, Jonathan J Lyons, Nima Parvaneh, Anh Thi Van Nguyen, Caterina Cancrini, Jennifer Heimall, Hanan Ahmed, Margaret L McKinnon, Yu-Lung Lau, Vivien Béziat, Suzanne C Tough
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease. The Journal of experimental medicine 220 (5) (2023)
Mehul Sharma, Daniel Leung, Mana Momenilandi, Lauren C W Jones, Lucia Pacillo, Alyssa E James, Jill R Murrell, Selket Delafontaine, Jesmeen Maimaris, Maryam Vaseghi-Shanjani, Kate L Del Bel, Henry Y Lu, Gilbert T Chua, Silvia Di Cesare, Oriol Fornes, Zhongyi Liu, Gigliola Di Matteo, Maggie P Fu, Donato Amodio, Issan Yee San Tam, Gavin Shueng Wai Chan, Ashish A Sharma, Joshua Dalmann, Robin van der Lee, Geraldine Blanchard-Rohner, Susan Lin, Quentin Philippot, Phillip Andrew Richmond, Jessica J Lee, Allison Matthews, Michael Seear, Alexandra K Turvey, Rachael L Philips, Terri F Brown-Whitehorn, Christopher J Gray, Kosuke Izumi, James R Treat, Kathleen H Wood, Justin Lack, Asya Khleborodova, Julie E Niemela, Xingtian Yang, Rui Liang, Lin Kui, Christina Sze-Man Wong, Grace Wing Kit Poon, Alexander Hoischen, Caspar I van der Made, Jing Yang, Koon Wing Chan, Jaime Sou Da Rosa Duque, Pamela Pui-Wah Lee, Marco Hok Kung Ho, Brian Hon-Yin Chung, Huong Thi Minh Le, Wanling Yang, Pejman Rohani, Ali Fouladvand, Hassan Rokni-Zadeh, Majid Changi-Ashtiani, Mohammad Miryounesi, Anne Puel, Mohammad Shahrooei, Andrea Finocchi, Paolo Rossi, Beatrice Rivalta, Cristina Cifaldi, Antonio Novelli, Chiara Passarelli, Stefania Arasi, Dominique M A Bullens, Kate Sauer, Tania Claeys, Catherine M Biggs, Emma Catherine Morris, Sergio D Rosenzweig, John J O'Shea, Wyeth W Wasserman, H Melanie Bedford, Clara D M van Karnebeek, Paolo Palma, Siobhan O Burns, Isabelle Meyts, Jean Laurent Casanova, Jonathan J Lyons, Nima Parvaneh, Anh Thi Van Nguyen, Caterina Cancrini, Jennifer Heimall, Hanan Ahmed, Margaret L McKinnon, Yu-Lung Lau, Vivien Béziat, Suzanne C Tough
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease. The Journal of experimental medicine 220 (5) (2023)
Nathan A Boggs, Xiaoping Sun, Jonathan J Lyons, Jeremy C McMurray, David M Rose, Eric M Pryor, Dean D Metcalfe, Irina Maric
Challenges in Applying Diagnostic Criteria for Systemic Mastocytosis. Blood advances (2023)
Mehul Sharma, Daniel Leung, Mana Momenilandi, Lauren C W Jones, Lucia Pacillo, Alyssa E James, Jill R Murrell, Selket Delafontaine, Jesmeen Maimaris, Maryam Vaseghi-Shanjani, Kate L Del Bel, Henry Y Lu, Gilbert T Chua, Silvia Di Cesare, Oriol Fornes, Zhongyi Liu, Gigliola Di Matteo, Maggie P Fu, Donato Amodio, Issan Yee San Tam, Gavin Shueng Wai Chan, Ashish A Sharma, Joshua Dalmann, Robin van der Lee, Geraldine Blanchard-Rohner, Susan Lin, Quentin Philippot, Phillip Andrew Richmond, Jessica J Lee, Allison Matthews, Michael Seear, Alexandra K Turvey, Rachael L Philips, Terri F Brown-Whitehorn, Christopher J Gray, Kosuke Izumi, James R Treat, Kathleen H Wood, Justin Lack, Asya Khleborodova, Julie E Niemela, Xingtian Yang, Rui Liang, Lin Kui, Christina Sze-Man Wong, Grace Wing Kit Poon, Alexander Hoischen, Caspar I van der Made, Jing Yang, Koon Wing Chan, Jaime Sou Da Rosa Duque, Pamela Pui-Wah Lee, Marco Hok Kung Ho, Brian Hon-Yin Chung, Huong Thi Minh Le, Wanling Yang, Pejman Rohani, Ali Fouladvand, Hassan Rokni-Zadeh, Majid Changi-Ashtiani, Mohammad Miryounesi, Anne Puel, Mohammad Shahrooei, Andrea Finocchi, Paolo Rossi, Beatrice Rivalta, Cristina Cifaldi, Antonio Novelli, Chiara Passarelli, Stefania Arasi, Dominique M A Bullens, Kate Sauer, Tania Claeys, Catherine M Biggs, Emma Catherine Morris, Sergio D Rosenzweig, John J O'Shea, Wyeth W Wasserman, H Melanie Bedford, Clara D M van Karnebeek, Paolo Palma, Siobhan O Burns, Isabelle Meyts, Jean Laurent Casanova, Jonathan J Lyons, Nima Parvaneh, Anh Thi Van Nguyen, Caterina Cancrini, Jennifer Heimall, Hanan Ahmed, Margaret L McKinnon, Yu-Lung Lau, Vivien Béziat, Suzanne C Tough
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease. The Journal of experimental medicine 220 (5) (2023)
Jack Chovanec, Ilker Tunc, Jason Hughes, Joseph Halstead, Allyson Mateja, Yihui Liu, Michael O'Connell, Jiwon Kim, Young Hwan Park, Qinlu Wang, Quang Trong Le, Mehdi Pirooznia, Neil Trivedi, Yun Bai, Yuzhi Yin, Amy P Hsu, Joshua J McElwee, Sheryce Lassiter, Celeste Nelson, Judy Bandoh, Thomas DiMaggio, Julij Selb, Matija Rijavec, Melody C Carter, Hirsh Komarow, Vito Sabato, Joshua A Steinberg, Kurt M Hafer, Elizabeth Feuille, Christopher S Hourigan, Justin Lack, Paneez Khoury, Irina Maric, Roberta Zanotti, Patrizia Bonadonna, Lawrence B Schwartz, Joshua D Milner, Sarah Camille Glover, Didier Gaston Ebo, Peter Korosec, George Caughey, Erica Brittain, Ben Busby, Dean D Metcalfe, Jonathan J Lyons
Genetically determining individualized clinical reference ranges for the biomarker tryptase can limit unnecessary procedures and unmask myeloid neoplasms. Blood advances (2022)
Ottavia Maria Delmonte, Jenna R E Bergerson, Tomoki Kawai, Hye Sun Kuehn, David H McDermott, Irene Cortese, Michael T Zimmermann, A Kerry Dobbs, Marita Bosticardo, Danielle Fink, Shamik Majumdar, Boaz Palterer, Francesca Pala, Nikita R Dsouza, Marie Pouzolles, Naomi Taylor, Katherine R Calvo, Stephen R Daley, Daniel Velez, Anahita Agharahimi, Katherine Myint-Hpu, Lesia K Dropulic, Jonathan J Lyons, Steven M Holland, Alexandra F Freeman, Rajarshi Ghosh, Morgan B Similuk, Julie E Niemela, Jennifer Stoddard, Douglas B Kuhns, Raul Urrutia, Sergio D Rosenzweig, Magdalena A Walkiewicz, Philip M Murphy, Luigi Daniele Notarangelo
SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulation. Blood 138 (12) (2021)
Jonathan J Lyons, Joshua D Milner
The clinical and mechanistic intersection of primary atopic disorders and inborn errors of growth and metabolism. Immunological reviews 287 (1) (2019)
Quang T Le, Jonathan J Lyons, Andrea N Naranjo, Ana Olivera, Robert A Lazarus, Dean D Metcalfe, Joshua D Milner, Lawrence B Schwartz
Impact of naturally forming human α/β-tryptase heterotetramers in the pathogenesis of hereditary α-tryptasemia. The Journal of experimental medicine 216 (10) (2019)
Jonathan J Lyons, Joshua D Milner
Primary atopic disorders. The Journal of experimental medicine 215 (4) (2018)
Vito Sabato, Jack Chovanec, Margaretha Faber, Joshua D Milner, Didier Ebo, Jonathan J Lyons
First Identification of an Inherited TPSAB1 Quintuplication in a Patient with Clonal Mast Cell Disease. Journal of clinical immunology 38 (4) (2018)
Chi A Ma, Jeffrey R Stinson, Yuan Zhang, Jordan K Abbott, Michael A Weinreich, Pia J Hauk, Paul R Reynolds, Jonathan J Lyons, Celeste G Nelson, Elisa Ruffo, Batsukh Dorjbal, Salomé Glauzy, Natsuko Yamakawa, Swadhinya Arjunaraja, Kelsey Voss, Jennifer Stoddard, Julie Niemela, Yu Zhang, Sergio D Rosenzweig, Joshua J McElwee, Thomas DiMaggio, Helen F Matthews, Nina Jones, Kelly D Stone, Alejandro Palma, Matías Oleastro, Emma Prieto, Andrea R Bernasconi, Geronimo Dubra, Silvia Danielian, Jonathan Zaiat, Marcelo A Marti, Brian Kim, Megan A Cooper, Neil Romberg, Eric Meffre, Erwin W Gelfand, Andrew L Snow, Joshua D Milner
Germline hypomorphic CARD11 mutations in severe atopic disease. Nature genetics 49 (8) (2017)
Yuan Zhang, Chi A Ma, Monica G Lawrence, Timothy J Break, Michael P O'Connell, Jonathan J Lyons, Diego B López, John S Barber, Yongge Zhao, Daniel L Barber, Alexandra F Freeman, Steven M Holland, Michail S Lionakis, Joshua D Milner
PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients. The Journal of experimental medicine 214 (9) (2017)
Jonathan J Lyons, Y Liu, C A Ma, Xiaomin Yu, M P O'Connell, M G Lawrence, Yuan Zhang, K Karpe, Ming Zhao, A M Siegel, K D Stone, C Nelson, Nina Jones, T DiMaggio, D N Darnell, Elvia C Mendoza-Caamal, Lorena Orozco-Orozco, Jason D Hughes, Joshua J McElwee, R J Hohman, P A Frischmeyer-Guerrerio, M E Rothenberg, Alexandra F Freeman, S M Holland, Joshua D Milner
ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans. The Journal of experimental medicine 214 (3) (2017)
Christina Lam, Carlos Ferreira, Donna Krasnewich, Camilo Toro, Lea Latham, Wadih M Zein, Tanya Lehky, Carmen Brewer, Eva H Baker, Audrey Thurm, Cristan A Farmer, Sergio D Rosenzweig, Jonathan J Lyons, John M Schreiber, Andrea Gropman, Shilpa Lingala, Marc G Ghany, Beth Solomon, Ellen F Macnamara, Mariska Davids, Constantine A Stratakis, Virginia Kimonis, William A Gahl, Lynne Wolfe
Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation. Genetics in medicine : official journal of the American College of Medical Genetics 19 (2) (2016)