D. Kavanagh's Profile

Role	Title	Level	Year	L/R
🐜	Biological Insights From 108 Schizophrenia-Associated Genetic Loci 300 auth. S. Ripke, B. Neale, A. Corvin, J. Walters, Kai-How Farh, P. Holmans, Phil H. Lee, B. Bulik-Sullivan, D. Collier, Hailiang Huang, T. Pers, I. Agartz, E. Agerbo, M. Albus, Madeline Alexander, ... F. Amin, S. Bacanu, M. Begemann, R. Belliveau, J. Bene, Sarah L Bergen, Elizabeth Bevilacqua, T. Bigdeli, D. Black, R. Bruggeman, N. Buccola, R. Buckner, W. Byerley, W. Cahn, Guiqing Cai, D. Campion, R. Cantor, V. Carr, N. Carrera, S. Catts, K. Chambert, R. Chan, Ronald Y. L. Chan, E. Chen, Wei Cheng, E. Cheung, S. Chong, C. Cloninger, D. Cohen, Nadine Cohen, P. Cormican, N. Craddock, J. Crowley, D. Curtis, M. Davidson, K. Davis, F. Degenhardt, J. Del Favero, D. Demontis, D. Dikeos, T. Dinan, S. Djurovic, G. Donohoe, Elodie Drapeau, J. Duan, F. Dudbridge, N. Durmishi, P. Eichhammer, J. Eriksson, V. Escott-Price, L. Essioux, A. Fanous, M. Farrell, J. Frank, L. Franke, R. Freedman, N. Freimer, M. Friedl, J. Friedman, M. Fromer, G. Genovese, L. Georgieva, I. Giegling, P. Giusti-Rodríguez, S. Godard, J. Goldstein, V. Golimbet, S. Gopal, J. Gratten, L. de Haan, C. Hammer, M. Hamshere, M. Hansen, T. Hansen, V. Haroutunian, A. Hartmann, F. Henskens, S. Herms, J. Hirschhorn, P. Hoffmann, A. Hofman, M. Hollegaard, D. Hougaard, M. Ikeda, I. Joa, A. Julià, R. Kahn, L. Kalaydjieva, Sena Karachanak-Yankova, J. Karjalainen, D. Kavanagh, M. Keller, J. Kennedy, A. Khrunin, Yunjung Kim, J. Kloviņš, J. Knowles, B. Konte, V. Kučinskas, Z. Kučinskienė, Hana Kuzelova-Ptackova, A. Kähler, C. Laurent, Jimmy Lee, S. H. Lee, S. Legge, B. Lerer, Miaoxin Li, Tao Li, K. Liang, J. Lieberman, S. Limborska, C. Loughland, J. Lubiński, J. Lönnqvist, M. Macek, P. Magnusson, B. Maher, W. Maier, J. Mallet, S. Marsal, M. Mattheisen, M. Mattingsdal, R. McCarley, C. Mcdonald, A. McIntosh, S. Meier, C. Meijer, B. Melegh, I. Melle, R. Mesholam-Gately, A. Metspalu, P. Michie, L. Milani, V. Milanova, Y. Mokrab, D. Morris, O. Mors, K. Murphy, R. Murray, I. Myin‐Germeys, B. Müller-Myhsok, M. Nelis, I. Nenadić, D. Nertney, G. Nestadt, K. Nicodemus, L. Nikitina-Zake, L. Nisenbaum, Annelie Nordin, E. O'callaghan, C. O’Dushlaine, F. O’Neill, Sang-Yun Oh, A. Olincy, L. Olsen, J. van os, C. Pantelis, G. Papadimitriou, S. Papiol, E. Parkhomenko, M. Pato, T. Paunio, M. Pejović-Milovančević, D. Perkins, O. Pietiläinen, J. Pimm, A. Pocklington, J. Powell, A. Price, A. Pulver, S. Purcell, D. Quested, H. Rasmussen, A. Reichenberg, M. Reimers, A. Richards, J. Roffman, P. Roussos, D. Ruderfer, V. Salomaa, A. Sanders, U. Schall, C. Schubert, T. Schulze, S. Schwab, E. Scolnick, R. Scott, L. Seidman, Jianxin Shi, E. Sigurdsson, T. Silagadze, J. Silverman, K. Sim, P. Slominsky, J. Smoller, H. So, C. Spencer, E. Stahl, H. Stefánsson, S. Steinberg, E. Stogmann, R. Straub, E. Strengman, J. Strohmaier, T. Stroup, M. Subramaniam, J. Suvisaari, D. Svrakic, J. Szatkiewicz, E. Söderman, S. Thirumalai, D. Toncheva, S. Tosato, J. Veijola, J. Waddington, D. Walsh, Dai Wang, Qiang Wang, B. Webb, M. Weiser, D. Wildenauer, N. Williams, Stephanie Williams, S. Witt, A. Wolen, Emily H. M. Wong, B. Wormley, H. Xi, C. Zai, Xue-bin Zheng, F. Zimprich, N. Wray, K. Stefánsson, P. Visscher, R. Adolfsson, O. Andreassen, D. Blackwood, E. Bramon, J. Buxbaum, A. Børglum, S. Cichon, A. Darvasi, E. Domenici, H. Ehrenreich, T. Esko, P. Gejman, M. Gill, H. Gurling, C. Hultman, N. Iwata, A. Jablensky, E. Jönsson, K. Kendler, G. Kirov, J. Knight, T. Lencz, D. Levinson, Qingqin S. Li, Jianjun Liu, A. Malhotra, S. Mccarroll, A. McQuillin, J. Moran, P. Mortensen, B. Mowry, M. Nöthen, R. Ophoff, M. Owen, A. Palotie, C. Pato, T. Petryshen, D. Posthuma, M. Rietschel, B. Riley, D. Rujescu, P. Sham, P. Sklar, D. St. Clair, D. Weinberger, J. Wendland, T. Werge, M. Daly, P. Sullivan, M. O’Donovan	12	2014	12 🐜
🐜	A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium 269 auth. C. Marshall, D. Howrigan, D. Merico, B. Thiruvahindrapuram, Wenting Wu, Douglas S. Greer, Danny Antaki, Aniket Shetty, P. Holmans, D. Pinto, Madhusudan Gujral, W. Brandler, Dheeraj Malholtra, Zhouzhi Wang, Karin V. Fuentes Fajarado, ... S. Ripke, I. Agartz, E. Agerbo, M. Albus, Madeline Alexander, F. Amin, J. Atkins, S. Bacanu, R. Belliveau, Sarah L Bergen, Marcelo Bertalan, Elizabeth Bevilacqua, T. Bigdeli, D. Black, R. Bruggeman, N. Buccola, R. Buckner, B. Bulik-Sullivan, W. Byerley, W. Cahn, Guiqing Cai, M. Cairns, D. Campion, R. Cantor, V. Carr, N. Carrera, S. Catts, K. Chambert, Wei Cheng, C. Cloninger, D. Cohen, P. Cormican, N. Craddock, B. Crespo-Facorro, J. Crowley, D. Curtis, M. Davidson, K. Davis, F. Degenhardt, J. D. Favero, L. DeLisi, D. Demontis, D. Dikeos, T. Dinan, S. Djurovic, G. Donohoe, Elodie Drapeau, J. Duan, F. Dudbridge, P. Eichhammer, J. Eriksson, V. Escott-Price, L. Essioux, A. Fanous, Kai-How Farh, M. Farrell, J. Frank, L. Franke, R. Freedman, N. Freimer, J. Friedman, A. Forstner, M. Fromer, G. Genovese, L. Georgieva, E. Gershon, I. Giegling, P. Giusti-Rodríguez, S. Godard, J. Goldstein, J. Gratten, L. Haan, M. Hamshere, M. Hansen, T. Hansen, V. Haroutunian, A. Hartmann, F. Henskens, S. Herms, J. Hirschhorn, P. Hoffmann, A. Hofman, M. Hollegaard, D. Hougaard, Hailiang Huang, M. Ikeda, I. Joa, A. Kähler, R. Kahn, L. Kalaydjieva, J. Karjalainen, D. Kavanagh, M. Keller, B. Kelly, J. Kennedy, Yunjung Kim, J. Knowles, B. Konte, C. Laurent, Phil H. Lee, S. Lee, S. Legge, B. Lerer, D. Levy, K. Liang, J. Lieberman, J. Lonnqvist, C. Loughland, P. Magnusson, B. Maher, W. Maier, J. Mallet, M. Mattheisen, M. Mattingsdal, R. McCarley, C. Mcdonald, A. McIntosh, S. Meier, C. Meijer, I. Melle, R. Mesholam-Gately, A. Metspalu, P. Michie, L. Milani, V. Milanova, Y. Mokrab, D. Morris, O. Mors, B. Müller-Myhsok, K. Murphy, R. Murray, I. Myin‐Germeys, I. Nenadić, D. Nertney, G. Nestadt, K. Nicodemus, L. Nisenbaum, Annelie Nordin, E. O'callaghan, C. O’Dushlaine, Sang-Yun Oh, A. Olincy, L. Olsen, F. O’Neill, J. Os, C. Pantelis, G. Papadimitriou, E. Parkhomenko, M. Pato, T. Paunio, D. Perkins, T. Pers, O. Pietiläinen, J. Pimm, A. Pocklington, J. Powell, A. Price, A. Pulver, S. Purcell, D. Quested, H. Rasmussen, A. Reichenberg, M. Reimers, A. Richards, J. Roffman, P. Roussos, D. Ruderfer, V. Salomaa, A. Sanders, A. Savitz, U. Schall, T. Schulze, S. Schwab, E. Scolnick, R. Scott, L. Seidman, Jianxin Shi, J. Silverman, J. Smoller, E. Söderman, C. Spencer, E. Stahl, E. Strengman, J. Strohmaier, T. Stroup, J. Suvisaari, D. Svrakic, J. Szatkiewicz, S. Thirumalai, P. Tooney, J. Veijola, P. Visscher, J. Waddington, D. Walsh, B. Webb, M. Weiser, D. Wildenauer, N. Williams, Stephanie Williams, S. Witt, A. Wolen, B. Wormley, N. Wray, J. Wu, C. Zai, R. Adolfsson, O. Andreassen, D. Blackwood, A. Børglum, E. Bramon, J. Buxbaum, S. Cichon, D. Collier, A. Corvin, M. Daly, A. Darvasi, E. Domenici, T. Esko, P. Gejman, M. Gill, H. Gurling, C. Hultman, N. Iwata, A. Jablensky, E. Jönsson, K. Kendler, G. Kirov, J. Knight, D. Levinson, Qingqin S. Li, S. Mccarroll, A. McQuillin, J. Moran, P. Mortensen, B. Mowry, M. Nöthen, R. Ophoff, M. Owen, A. Palotie, C. Pato, T. Petryshen, D. Posthuma, M. Rietschel, B. Riley, D. Rujescu, P. Sklar, D. Clair, J. Walters, T. Werge, P. Sullivan, M. O’Donovan, S. Scherer, B. Neale, J. Sebat	10	2016	10 🐜
🐜	Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. 18 auth. J. Caprioli, M. Noris, S. Brioschi, G. Pianetti, F. Castelletti, P. Bettinaglio, C. Mele, E. Bresin, L. Cassis, S. Gamba, ... Francesca Porrati, Sara Bucchioni, G. Monteferrante, C. J. Fang, M. Liszewski, D. Kavanagh, J. Atkinson, G. Remuzzi	9	2006	9 🐜
🐜	The ExAC browser: displaying reference data information from over 60 000 exomes 14 auth. K. Karczewski, B. Weisburd, B. Thomas, M. Solomonson, D. Ruderfer, D. Kavanagh, T. Hamamsy, M. Lek, K. Samocha, Beryl B. Cummings, ... Daniel P Birnbaum, The Exome Aggregation Consortium, M. Daly, D. MacArthur	9	2016	9 🐜
🐜	Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference. 55 auth. T. Goodship, H. Cook, F. Fakhouri, F. Fervenza, V. Frémeaux-Bacchi, D. Kavanagh, C. Nester, M. Noris, M. Pickering, S. R. Córdoba, L. Roumenina, L. Roumenina, L. Roumenina, S. Sethi, Richard J. H. Smith, ... C. Alpers, G. Appel, G. Ardissino, G. Ariceta, M. Arıcı, A. Bagga, I. Bajema, M. Blasco, Linda Burke, T. Cairns, M. Carratalá, V. D’Agati, M. Daha, A. S. Vriese, M. Dragon-Durey, A. Fogo, M. Galbusera, D. Gale, Hermann Haller, Sally Johnson, M. Józsi, D. Karpman, Lynne Lanning, M. L. Quintrec, C. Licht, C. Loirat, F. Monfort, B. Morgan, L. Noël, M. O'shaughnessy, M. Rabant, E. Rondeau, P. Ruggenenti, N. Sheerin, J. Smith, Fabrizio Spoleti, J. Thurman, N. Kar, M. Vivarelli, P. Zipfel	9	2017	9 🐜
🦁	Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome. 10 auth. D. Kavanagh, E. J. Kemp, Elizabeth Mayland, R. Winney, J. Duffield, G. Warwick, ... A. Richards, Roy Ward, J. Goodship, T. Goodship	8	2005	8 🦁
🐜	C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy 37 auth. A. Richards, A. M. van den Maagdenberg, J. Jen, D. Kavanagh, P. Bertram, D. Spitzer, M. Liszewski, Maria-Louise Barilla-LaBarca, G. Terwindt, Y. Kasai, M. McLellan, Mark Gilbert Grand, K. R. Vanmolkot, B. de Vries, Jijun Wan, ... M. J. Kane, H. Mamsa, Ruth Schäfer, A. Stam, J. Haan, P. de Jong, C. Storimans, M. V. van Schooneveld, J. Oosterhuis, A. Gschwendter, M. Dichgans, K. Kotschet, S. Hodgkinson, T. A. Hardy, M. Delatycki, R. Hajj-Ali, P. Kothari, Stan F. Nelson, R. Frants, R. Baloh, M. Ferrari, J. Atkinson	8	2007	8 🐜
🐜	Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome. 13 auth. I. Moore, L. Strain, I. Pappworth, D. Kavanagh, P. Barlow, A. Herbert, C. Schmidt, Scott J. Staniforth, Lucy V. Holmes, Roy Ward, ... Lynn Morgan, T. Goodship, K. Marchbank	8	2010	8 🐜
🐜	Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration 16 auth. J. Seddon, Yi Yu, Elizabeth C. Miller, Robyn C Reynolds, P. L. Tan, Sivakumar Gowrisankar, J. Goldstein, M. Triebwasser, Holly E. Anderson, J. Zerbib, ... D. Kavanagh, E. Souied, N. Katsanis, M. Daly, J. Atkinson, S. Raychaudhuri	8	2013	8 🐜
🐜	Mutations in Complement Regulatory Proteins Predispose to Preeclampsia: A Genetic Analysis of the PROMISSE Cohort 10 auth. J. Salmon, C. Heuser, M. Triebwasser, M. Liszewski, D. Kavanagh, L. Roumenina, ... D. Branch, T. Goodship, V. Frémeaux-Bacchi, J. Atkinson	8	2011	8 🐜
🐜	Extended haplotypes in the complement factor H (CFH) and CFH‐related (CFHR) family of genes protect against age‐related macular degeneration: Characterization, ethnic distribution and evolutionary implications 17 auth. G. Hageman, L. Hancox, Andrew J Taiber, K. Gehrs, Don H. Anderson, L. V. Johnson, M. Radeke, D. Kavanagh, A. Richards, J. Atkinson, ... S. Meri, J. Bergeron, J. Zernant, J. Merriam, B. Gold, R. Allikmets, M. Dean	8	2006	8 🐜
🐜	Atypical aHUS: State of the art. 13 auth. C. Nester, T. Barbour, Santiago Rodríquez de Córdoba, M. Dragon-Durey, V. Frémeaux-Bacchi, T. Goodship, D. Kavanagh, M. Noris, M. Pickering, P. Sánchez-Corral, ... C. Skerka, P. Zipfel, Richard J. H. Smith	8	2015	8 🐜
🐜	C3 glomerulopathy — understanding a rare complement-driven renal disease 18 auth. Richard J. H. Smith, G. Appel, A. Blom, H. Cook, V. D’Agati, F. Fakhouri, V. Frémeaux-Bacchi, M. Józsi, D. Kavanagh, John D Lambris, ... M. Noris, M. Pickering, G. Remuzzi, S. R. de Córdoba, S. Sethi, J. van der Vlag, P. Zipfel, C. Nester	8	2019	8 🐜