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Stephen P. Robertson

University of Otago

60H指数
279论文数
1.2W被引数
收录论文 111
发表时间
Impaired retinoic acid receptor-γ signalling underlies a heritable form of urothelial keratinising squamous metaplasia受损的视黄酸受体-γ信号通路是遗传性尿路上皮角化鳞状细胞化生的潜在原因。
err2026-03-13
err0
errOAAI
errKaya Fukushima; Nicole Avery; Jade Desjardins; Benjamin J. Halliday; Zandra A. Jenkins; Robert Porteous; Tim Morgan; Padmini Parthasarathy; Michael Lau; Michael W. Vincent; Karen J. Liu; Stephen R.F. Twigg; Stephen P. Robertson
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A functional role for septin-2 in the maintenance of the axon initial segment and in human cognitive development
errBrain
IF11.7
err2025-12-17
err0
errOAAI
errLuisa Weiss; Macarena Pavez; Anastasia Labudina; Liliia Andriichuk; Owen Jones; Amy Jones; Deanna Barwick; Zandra Jenkins; Indranil Basak; Tim Morgan; Teresa Neuhann; Julia Rankin; Jacques Giltay; Emanuele Agolini; Antonio Novelli; Antonio Pizzuti; Daniel C Koboldt; Swetha Ramadesikan; Leeran B Dublin-Ryan; Stephanie Hughes; Nataylia Di Donato; Greg Gimenez; Takashi Namba; Laura F Gumy; Stephen P Robertson
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Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformation双侧额叶室管膜下结节性异位:一种独特的皮层畸形
err2025-12-01
err0
PREAI
errHoogwijs, Ine; Mandelstam, Simone A.; Mcgillivray, George; Halliday, Benjamin J.; Yiu, Eppie M.; Macdonald-Laurs, Emma; Perry, David; Patel, Rakesh; Gabbett, Michael; Patel, Chirag; Malone, Stephen; Fahey, Michael; Gill, Deepak; Field, Mike; Delatycki, Martin B.; Mohammad, Shekeeb; Berkovic, Samuel F.; Scheffer, Ingrid E.; Lockhart, Paul J.; Jackson, Graeme D.; Jansen, Anna C.; Robertson, Stephen P.; Leventer, Richard J.
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Further delineation of the SCAF4-associated neurodevelopmental disorder
err2024-12-12
err0
errOAAI
errSchmid, Cosima M.; Gregor, Anne; Ruiz, Anna; Manso Bazus, Carmen; Herman, Isabella; Ammouri, Farah; Kotzaeridou, Urania; Mcniven, Vanda; Dupuis, Lucie; Steindl, Katharina; Begemann, Anais; Rauch, Anita; Suter, Aude-Annick; Isidor, Bertrand; Mercier, Sandra; Nizon, Mathilde; Cogne, Benjamin; Deb, Wallid; Besnard, Thomas; Haack, Tobias B.; Falb, Ruth J.; Mueller, Amelie J.; Linden, Tobias; Haldeman-Englert, Chad R.; Ockeloen, Charlotte W.; Mattioli, Francesca; Reymond, Alexandre; Ibrahim, Nazia; Naz, Shagufta; Lacaze, Elodie; Bassetti, Jennifer A.; Hoefele, Julia; Brunet, Theresa; Riedhammer, Korbinian M.; Elloumi, Houda Z.; Person, Richard; Zou, Fanggeng; Kahle, Juliette J.; Cremer, Kirsten; Schmidt, Axel; Delrue, Marie-Ange; Almeida, Pedro M.; Ramos, Fabiana; Srivastava, Siddharth; Quinlan, Aisling; Robertson, Stephen; Manka, Eva; Kuechler, Alma; Spranger, Stephanie; Nowaczyk, Malgorzata J. M.; Elshafie, Reem M.; Alsharhan, Hind; Hillman, Paul R.; Dunnington, Leslie A.; Braakman, Hilde M. H.; Mckee, Shane; Moresco, Angelica; Ignat, Andrea-Diana; Newbury-Ecob, Ruth; Banneau, Guillaume; Patat, Olivier; Kuerbitz, Jeffrey; Rzucidlo, Susan; Sell, Susan S.; Gordon, Patricia; Schuhmann, Sarah; Reis, Andre; Halleb, Yosra; Stoeva, Radka; Keren, Boris; Al Masseri, Zainab; Tuemer, Zeynep; Hammer-Hansen, Sophia; Krueger Solyst, Sofus; Steigerwald, Connolly G.; Abreu, Nicolas J.; Faust, Helene; Mueller-Nedebock, Amica; Tran Mau-Them, Frederic; Sticht, Heinrich; Zweier, Christiane
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Aberrant connectivity of the lateralized readiness system in non-syndromic congenital mirror movements
err2024-11-01
err0
PREAI
errLu, Xueyao; Franz, Elizabeth A.; Robertson, Stephen P.; Markie, David
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The hinge-1 domain of Flna is not necessary for diverse physiological functions in mice
err2024-08-31
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errOAAI
errWade, Emma M.; Goodin, Elizabeth A.; Morgan, Tim; Pereira, Stephana; Woolley, Adele G.; Jenkins, Zandra A.; Daniel, Philip B.; Robertson, Stephen P.
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Idiopathic juvenile osteoporosis-a polygenic disorder?
err2024-07-29
err0
errOAAI
errWade, Emma; Mulholland, Katie; Shaw, Ian; Cundy, Tim; Robertson, Stephen
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Further delineation of short-chain enoyl-CoA hydratase deficiency in the Pacific population
err2024-07-01
err2
PREAI
errBernhardt, Isaac; Frajman, Leah E.; Ryder, Bryony; Andersen, Erik; Wilson, Callum; Mckeown, Colina; Anderson, Tim; Coman, David; Vincent, Andrea L.; Buchanan, Christina; Roxburgh, Richard; Pitt, James; De Hora, Mark; Christodoulou, John; Thorburn, David R.; Wilson, Francessa; Drake, Kylie M.; Leask, Megan; Yardley, Anne-Marie; Merriman, Tony; Robertson, Stephen; Compton, Alison G.; Glamuzina, Emma
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Clustered de novo start-loss variants in GLUL result in a developmental and epileptic encephalopathy via stabilization of glutamine synthetase
err2024-04-01
err4
PREAI
errJones, Amy G.; Aquilino, Matilde; Tinker, Rory J.; Duncan, Laura; Jenkins, Zandra; Carvill, Gemma L.; Deward, Stephanie J.; Grange, Dorothy K.; Hajianpour, Mj; Halliday, Benjamin J.; Holder-Espinasse, Muriel; Horvath, Judit; Maitz, Silvia; Nigro, Vincenzo; Morleo, Manuela; Paul, Victoria; Spencer, Careni; Esterhuizen, Alina I.; Polster, Tilman; Spano, Alice; Gomez-Lozano, Ines; Kumar, Abhishek; Poke, Gemma; Phillips, John A.; Underhill, Hunter R.; Gimenez, Gregory; Namba, Takashi; Robertson, Stephen P.
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Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711
err2023-12-01
err0
errOAAI
errWang, Jiyong; Foroutan, Aidin; Richardson, Ellen; Skinner, Steven A.; Reilly, Jack; Kerkhof, Jennifer; Curry, Cynthia J.; Tarpey, Patrick S.; Robertson, Stephen P.; Maystadt, Isabelle; Keren, Boris; Dixon, Joanne W.; Skinner, Cindy; Stapleton, Rachel; Ruaud, Lyse; Gumus, Evren; Lakeman, Phillis; Alders, Marielle; Tedder, Matthew L.; Schwartz, Charles E.; Friez, Michael J.; Sadikovic, Bekim; Stevenson, Roger E.
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Familial aggregation of keratinising desquamative squamous metaplasia in the urinary tract
err2023-08-29
err0
PREAI
errAvery, Nicole; Fukushima, Kaya; Guan, Guangzhao; Praganta, Jesslyn; Rich, Alison; Vincent, Michael; Robertson, Stephen
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Metformin rescues migratory deficits of cells derived from patients with periventricular heterotopia二甲双胍可挽救脑室周围异位症患者的细胞迁移缺陷
err2023-08-23
err0
errOAAI
errBressan, Cedric; Snapyan, Marta; Snapyan, Marina; Klaus, Johannes; di Matteo, Francesco; Robertson, Stephen P.; Treutlein, Barbara; Parent, Martin; Cappello, Silvia; Saghatelyan, Armen
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Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature
err2023-08-16
err7
errOAAI
errPeluso, Francesca; Caraffi, Stefano G.; Contro, Gianluca; Valeri, Lara; Napoli, Manuela; Carboni, Giorgia; Seth, Alka; Zuntini, Roberta; Coccia, Emanuele; Astrea, Guja; Bisgaard, Anne-Marie; Ivanovski, Ivan; Maitz, Silvia; Brischoux-Boucher, Elise; Carter, Melissa T.; Dentici, Maria Lisa; Devriendt, Koenraad; Bellini, Melissa; Digilio, Maria Cristina; Doja, Asif; Dyment, David A.; Farholt, Stense; Ferreira, Carlos R.; Wolfe, Lynne A.; Gahl, William A.; Gnazzo, Maria; Goel, Himanshu; Gronborg, Sabine Weller; Hammer, Trine; Iughetti, Lorenzo; Kleefstra, Tjitske; Koolen, David A.; Lepri, Francesca Romana; Lemire, Gabrielle; Louro, Pedro; McCullagh, Gary; Madeo, Simona F.; Milone, Annarita; Milone, Roberta; Nielsen, Jens Erik Klint; Novelli, Antonio; Ockeloen, Charlotte W.; Pascarella, Rosario; Pippucci, Tommaso; Ricca, Ivana; Robertson, Stephen P.; Sawyer, Sarah; Smeland, Marie Falkenberg; Stegmann, Sander; Stumpel, Constanze T.; Goel, Amy; Taylor, Juliet M.; Barbuti, Domenico; Soresina, Annarosa; Bedeschi, Maria Francesca; Battini, Roberta; Cavalli, Anna; Fusco, Carlo; Iascone, Maria; Van Maldergem, Lionel; Venkateswaran, Sunita; Zuffardi, Orsetta; Vergano, Samantha; Garavelli, Livia; Bayat, Allan
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Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim Syndrome
err2022-10-13
err1
errOAAI
errHalliday, B. J.; Baynam, G.; Ewans, L.; Greenhalgh, L.; Leventer, R. J.; Pilz, D. T.; Sachdev, R.; Scheffer, I. E.; Markie, D. M.; McGillivray, G.; Robertson, S. P.; Mandelstam, S.
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Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders遗传性神经发育障碍全基因组DNA甲基化谱的功能相关性
err2022-08-21
err46
errOAAI
errLevy, Michael A.; Relator, Raissa; McConkey, Haley; Pranckeviciene, Erinija; Kerkhof, Jennifer; Barat-Houari, Mouna; Bargiacchi, Sara; Biamino, Elisa; Bralo, Maria Palomares; Cappuccio, Gerarda; Ciolfi, Andrea; Clarke, Angus; DuPont, Barbara R.; Elting, Mariet W.; Faivre, Laurence; Fee, Timothy; Ferilli, Marco; Fletcher, Robin S.; Cherick, Florian; Foroutan, Aidin; Friez, Michael J.; Gervasini, Cristina; Haghshenas, Sadegheh; Hilton, Benjamin A.; Jenkins, Zandra; Kaur, Simranpreet; Lewis, Suzanne; Louie, Raymond J.; Maitz, Silvia; Milani, Donatella; Morgan, Angela T.; Oegema, Renske; Ostergaard, Elsebet; Pallares, Nathalie R.; Piccione, Maria; Plomp, Astrid S.; Poulton, Cathryn; Reilly, Jack; Rius, Rocio; Robertson, Stephen; Rooney, Kathleen; Rousseau, Justine; Santen, Gijs W. E.; Santos-Simarro, Fernando; Schijns, Josephine; Squeo, Gabriella M.; St John, Miya; Thauvin-Robinet, Christel; Traficante, Giovanna; van der Sluijs, Pleuntje J.; Vergano, Samantha A.; Vos, Niels; Walden, Kellie K.; Azmanov, Dimitar; Balci, Tugce B.; Banka, Siddharth; Gecz, Jozef; Henneman, Peter; Lee, Jennifer A.; Mannens, Marcel M. A. M.; Roscioli, Tony; Siu, Victoria; Amor, David J.; Baynam, Gareth; Bend, Eric G.; Boycott, Kym; Brunetti-Pierri, Nicola; Campeau, Philippe M.; Campion, Dominique; Christodoulou, John; Dyment, David; Esber, Natacha; Fahrner, Jill A.; Fleming, Mark D.; Genevieve, David; Heron, Delphine; Husson, Thomas; Kernohan, Kristin D.; McNeill, Alisdair; Menke, Leonie A.; Merla, Giuseppe; Prontera, Paolo; Rockman-Greenberg, Cheryl; Schwartz, Charles; Skinner, Steven A.; Stevenson, Roger E.; Vincent, Marie; Vitobello, Antonio; Tartaglia, Marco; Alders, Marielle; Tedder, Matthew L.; Sadikovic, Bekim
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Intervertebral disc degeneration is rescued by TGFβ/BMP signaling modulation in an ex vivo filamin B mouse model
err2022-04-26
err5
errOAAI
errZieba, Jennifer; Forlenza, Kimberly N.; Heard, Kelly; Martin, Jorge H.; Bosakova, Michaela; Cohn, Daniel H.; Robertson, Stephen P.; Krejci, Pavel; Krakow, Deborah
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