A

ahmadizar, Fariba, Vijverberg, Susanne J H, Arets, Hubertus G M, de Boer, Anthonius, Lang, Jason E, Kattan, Meyer, Palmer, Colin N A, Mukhopadhyay, Somnath, Turner, Steve and Maitland-van der Zee, Anke H (2016) Childhood obesity in relation to poor asthma control and exacerbation: a meta-analysis. European Respiratory Journal, 48 (4). pp. 1063-1073. ISSN 0903-1936

B

Bagheri, Hani, Badduke, Chansonette, Qiao, Ying, Colnaghi, Rita, Abramowicz, Iga, Alcantara, Diana, Dunham, Christopher, Wen, Jiadi, Wlldln, Robert S, Nowaczyk, Malgorzata J M, Elchmeyer, Jennifer, Lehman, Anna, Maranda, Bruno, Martell, Sally, Shan, Xianghong, Lewis, Suzanne M E, O'Driscoll, Mark, Gregory-Evans, Cheryl Y and Rajcan-Separovic, Evica (2016) Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis. Journal of Clinical Investigation Insight, 1 (3). e85461 1-20. ISSN 2379-3708

Basu, K, Palmer, C N A, Lipworth, B J, Irwin, W H, Terron-Kwiatkowski, A, Zhao, Y, Liao, H, Smith, F J D, Mitra, A and Mukhopadhyay, S (2008) Filaggrin null mutations are associated with increased asthma exacerbations in children and young adults. Allergy, 63 (9). pp. 1211-1217. ISSN 0105-4538

Basu, Kaninika, Inglis, Sarah K, Bremner, Stephen A, Ramsay, Rebecca, Abd, Ali, Rabe, Heike, Strange, Elizabeth, Phillips, Veronica, Seddon, Paul, Tavendale, Roger, Memon, Anjum, Palmer, Colin N A, Fidler, Katy and Mukhopadhyay, Somnath (2020) Filaggrin gene defects are associated with eczema, wheeze and nasal disease during infancy: prospective study. Journal of Allergy and Clinical Immunology, 146 (3). pp. 681-682. ISSN 0091-6749

Bisgaard, Hans, Simpson, Angela, Palmer, Colin N.A., Bonnelykke, Klaus, Mclean, Irwin, Mukhopadhyay, Somnath, Pipper, Christian B., Halkjaer, Liselotte B., Lipworth, Brian, Hankinson, Jenny, Woodcock, Ashley and Custovic, Adnan (2008) Gene-Environment Interaction in the Onset of Eczema in Infancy: Filaggrin Loss-of-Function Mutations Enhanced by Neonatal Cat Exposure. PLoS Medicine, 5 (6). 934 -940. ISSN 1549-1277

S

Saunders, Sean P, Mukhopadhyay, Somnath and et al, (2013) Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects. Journal of Allergy and Clinical Immunology, 132 (5). pp. 1121-1129. ISSN 0091-6749

T

Turner, Steve, Francis, Ben, Vijverberg, Susanne, Pino-Yanes, Maria, Maitland-van der Zee, Anke H, Basu, Kaninika, Bignell, Lauren, Mukhopadhyay, Somnath, Tavendale, Roger, Palmer, Colin, Hawcutt, Daniel, Pirmohamed, Munir, Burchard, Esteban G and Lipworth, Brian (2016) Childhood asthma exacerbations and the Arg16 b2-receptor polymorphism: a meta-analysis stratified by treatment. Journal of Allergy and Clinical Immunology, 138 (1). 107-113.e5. ISSN 0091-6749

Turner, Steve, Francis, Ben, Wani, Nuha, Vijverberg, Susanne, Pino-Yanes, Maria, Mukhopadhyay, Somnath, Tavendale, Roger, Palmer, Colin, Burchard, Esteban G, Kebede Merid, Simon, Melen, Erik, Maitland-van der Zee, Anke H and Pharmacogenomics in Childhood Asthma Consortium, (2018) Variants in genes coding for Glutathione S-Transferases and asthma outcomes in children. Pharmacogenomics, 19 (8). ISSN 1462-2416

V

Van Esch, Hilde, Colnaghi, Rita, Freson, Kathleen, Starokadomskyy, Petro, Zankl, Andreas, Backx, Liesbeth, Abramowicz, Iga, Outwin, Emily, Rohena, Luis, Faulkner, Claire, Leong, Gary M, Newbury-Ecob, Ruth A, Challis, Rachel C, Õunap, Katrin, Jaeken, Jacques, Seuntjens, Eve, Devriendt, Koen, Burstein, Ezra, Low, Karen J and O'Driscoll, Mark (2019) Defective DNA polymerase α-primase leads to X-linked intellectual disability associated with severe growth retardation, microcephaly, and hypogonadism. American Journal of Human Genetics, 104 (5). pp. 957-967. ISSN 1537-6605

Vijverberg, Susanne J, Koster, Ellen S, Tavendale, Roger, Leusink, Maarten, Koenderman, Leo, Raaijmakers, Jan A M, Postma, Dirkje S, Koppelman, Gerard H, Turner, Steve W, Mukhopadhyay, Somnath, Tse, Sze Man, Tantisira, Kelan G, Hawcutt, Daniel B, Francis, Ben, Pirmohamed, Munir, Pino-Yanes, Mario, Eng, Celeste, Burchard, Esteban G, Palmer, Colin N A and Maitland-van der Zee, Anke H (2015) ST13 polymorphisms and their effect on exacerbations in steroid-treated asthmatic children and young adults. Clinical & Experimental Allergy, 45 (6). pp. 1051-1059. ISSN 0954-7894

Vijverberg, Susanne J H, Tavendale, Roger, Leusink, Maarten, Koenderman, Leo, Raaijmakers, Jan AM, Postma, Dirkje S, Koppelman, Gerard H, Turner, Steve W, Mukhopadhyay, Somnath, Palmer, Colin N A and Maitland-van der Zee, Anke Hilse (2014) Pharmacogenetic analysis of GLCCI1 in three north European pediatric asthma populations with a reported use of inhaled corticosteroids. Pharmacogenomics, 15 (6). pp. 799-806. ISSN 1462-2416