ScholarIQanswers from OpenAlex & ORCID
Pak C. Sham
ResearcherPublications, citations & collaboration network
Pak C. Sham is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Pak C. Sham have?
ScholarIQindexed works
Pak C. Sham has 1,087 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Pak C. Sham have?
ScholarIQcitation count
Pak C. Sham has 121,589 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Pak C. Sham?
ScholarIQh-index
Pak C. Sham has an h-index of 135 in OpenAlex.
What is the i10-index of Pak C. Sham?
ScholarIQi10-index
Pak C. Sham has an i10-index of 682 in OpenAlex.
What is the ORCID of Pak C. Sham?
ScholarIQorcid
The ORCID for Pak C. Sham is on the source record.
What is the OpenAlex record for Pak C. Sham?
ScholarIQopenalex
The OpenAlex for Pak C. Sham is on the source record.
What are the most-cited papers on Pak C. Sham?
ScholarIQmost cited works
The contribution of cannabis use to variation in the incidence of psychotic disorder across Europe (EU-GEI): a multicentre case-control study
Marta Di Forti, Diego Quattrone, Tom P. Freeman, Giada Tripoli, Charlotte Gayer‐Anderson, Harriet Quigley, Victoria Rodríguez, Hannah E. Jongsma, Laura Ferraro, Caterina La Cascia, Daniele La Barbera, Ilaria Tarricone, Domenico Berardi, Andreı̈ Szöke, Celso Arango, Andrea Tortelli, Eva Velthorst, Miquel Bernardo, Cristina Marta Del‐Ben, Paulo Rossi Menezes, Jean-Paul Selten, Peter B. Jones, James B. Kirkbride, Bart P. F. Rutten, Lieuwe de Haan, Pak C. Sham, Jim van Os, Cathryn M. Lewis, Michael T. Lynskey, Craig Morgan, Robin Murray, Sílvia Amoretti, Manuel Arrojo, Grégoire Baudin, Stephanie Beards, Miquel Bernardo, Julio Bobes, Chiara Bonetto, Bibiana Cabrera, Ãngel Carracedo, Thomas Charpeaud, Javier Costas, Doriana Cristofalo, Pedro Cuadrado, Covadonga M. Díaz‐Caneja, Aziz Ferchiou, Nathalie Franke, Flora Frijda, Enrique García Bernardo, Paz Garcia-Portilla, Emiliano González, Kathryn Hubbard, Stéphane Jamain, Estela Jiménez‐López, Marion Leboyer, Gonzalo López Montoya, Esther Lorente-Rovira, Camila Marcelino Loureiro, Giovanna Marrazzo, Covadonga Martínez, Mario De Matteis, Elles Messchaart, Ma Dolores Moltó, Juan Nácher, Ma Soledad Olmeda, Mara Parellada, Javier González‐Peñas, Baptiste Pignon, Marta Rapado, Jean‐Romain Richard, José Juan Rodríguez Solano, Laura Roldán Díaz, Mirella Ruggeri, Pilar A. Sáiz, Emilio Sánchez, Julio Sanjuán, Crocettarachele Sartorio, Franck Schürhoff, Fabio Seminerio, Rosana Shuhama, Lucia Sideli, Simona A. Stilo, Fabian Termorshuizen, Sarah Tosato, Anne-Marie Tronche, Daniella van Dam, Els van der Ven
A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders.
David Collier, G. Stöber, Tao Li, Armin Heils, Marco Catalano, Daniela Di Bella, María J. Arranz, Robin Murray, Homero Vallada, Dietmar Bengel, C. R. Müller, G.W. Roberts, Enrico Smeraldi, George Kirov, Pak C. Sham, Klaus‐Peter Lesch
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes
L Feldman, K Fleischman, S Medad, Ruud B. Minderaa, Urs Müller, Aisling Mulligan, K Rabin, Lena Johansson, Pak C. Sham, Philip Asherson, Faraone, SV, Margaret Thompson, Michael Gill, Eric Taylor, Steinhausen, HC, Richard P. Ebstein, Joseph A. Sergeant, Aribert Rothenberger, Herbert Roeyers, Robert Plomin, Oades, RD, Ana Miranda, Peter McGuffin, Iris Manor, Jonna Kuntsi, J Eisenberg, SonugaBarke, E, Tobias Banaschewski, Ian Craig, Rachel Barrett, Anne Weeks, Lamprini Psychogiou, Henrik Uebel, J Sorohan, Vaheshta Sethna, Nanda Rommelse, Marieke E. Altink, Frits Boer, Penny Andreou, Jo Knight, Eric Fliers, HoweForbes, R, Allan Goldfarb, Keeley J. Brookes, Xiaohui Xu, W. Chen, Desmond Campbell, Kaixin Zhou, Benjamin M. Neale, Jan K. Buitelaar, Cathelijne J.M. Buschgens, Naomi Lowe, R Aneey, Louise Butler, Alexander Heise, Isabel Gabriëls, Hanna Christiansen, Barbara Franke, KornLubetzki, I, Rafaela Marco, R Arnold, Fernando Mulas
International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases
Kym M. Boycott, Ana Rath, Jessica X. Chong, Taila Hartley, Fowzan S. Alkuraya, Gareth Baynam, Anthony J. Brookes, Michael Brudno, Ãngel Carracedo, Johan T. den Dunnen, Stephanie O. M. Dyke, Xavier Estivill, Jack Goldblatt, Catherine Gonthier, Stephen C. Groft, Marta Gut, Ada Hamosh, Philip Hieter, Sophie Höhn, Matthew E. Hurles, Petra Kaufmann, Bartha Maria Knoppers, Jeffrey P. Krischer, Milan Maçek, Gert Matthijs, Annie Olry, Samantha Parker, Justin Paschall, Anthony Philippakis, Heidi L. Rehm, Peter N. Robinson, Pak C. Sham, Румен Стефанов, Domenica Taruscio, Divya Unni, Megan R. Vanstone, Feng Zhang, Han G. Brunner, Michael J. Bamshad, Hanns Lochmüller
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
Wanling Yang, Nan Shen, Dong‐Qing Ye, Qiji Liu, Yan Zhang, Xiaoxia Qian, Nattiya Hirankarn, Dingge Ying, Hai‐Feng Pan, Chi Chiu Mok, Tak Mao Chan, Raymond Woon Sing Wong, Ka Wing Lee, Mo Yin Mok, Sik Nin Wong, Alexander Moon Ho Leung, Xiang-Pei Li, Yingyos Avihingsanon, Chun‐Ming Wong, Tsz Leung Lee, M. Ho, Pamela Lee, Yuk Kwan Chang, Philip H. Li, Ruo-Jie Li, Lu Zhang, Wilfred Hing Sang Wong, Irene Oi‐Lin Ng, Chak Sing Lau, Pak C. Sham, YL Lau