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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Disease and SLC16A1[original query]
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.
European journal of endocrinology / European Federation of Endocrine Societies 2013 Jan .
Kapoor RR, Flanagan SE, Arya VB, Shield JP, Ellard S, Hussain K
Associations of common variants in the SLC16A11, TCF7L2, and ABCA1 genes with pediatric-onset type 2 diabetes and related glycemic traits in families: A case-control and case-parent trio study.
Pediatric diabetes 2017 Jan .
Miranda-Lora América L, Cruz Miguel, Molina-Díaz Mario, Gutiérrez Jorge, Flores-Huerta Samuel, Klünder-Klünder Migu
Systematic analyses of regulatory variants in DNase I hypersensitive sites identified two novel lung cancer susceptibility loci.
Carcinogenesis 2018 12 40 (3): 432-440.
Dai Juncheng, Li Zhihua, Amos Christopher I, Hung Rayjean J, Tardon Adonina, Andrew Angeline S, Chen Chu, Christiani David C, Albanes Demetrios, van der Heijden Erik H F M, Duell Eric J, Rennert Gad, Mckay James D, Yuan Jian-Min, Field John K, Manjer Jonas, Grankvist Kjell, Le Marchand Loic, Teare M Dawn, Schabath Matthew B, Aldrich Melinda C, Tsao Ming-Sound, Lazarus Philip, Lam Stephen, Bojesen Stig E, Arnold Susanne, Wu Xifeng, Haugen Aage, Janout Vladimir, Johansson Mikael, Brhane Yonathan, Fernandez-Somoano Ana, Kiemeney Lambertus A, Davies Michael P A, Zienolddiny Shanbeh, Hu Zhibin, Shen Hongbi
Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene. GWAS Catalog
Carcinogenesis 2020 05 41 (3): 284-295.
Avitabile Marianna, Succoio Mariangela, Testori Alessandro, Cardinale Antonella, Vaksman Zalman, Lasorsa Vito Alessandro, Cantalupo Sueva, Esposito Matteo, Cimmino Flora, Montella Annalaura, Formicola Daniela, Koster Jan, Andreotti Virginia, Ghiorzo Paola, Romano Maria Fiammetta, Staibano Stefania, Scalvenzi Massimiliano, Ayala Fabrizio, Hakonarson Hakon, Corrias Maria Valeria, Devoto Marcella, Law Matthew H, Iles Mark M, Brown Kevin, Diskin Sharon, Zambrano Nicola, Iolascon Achille, Capasso Mar
Clinical and Genetic Characterization of 153 Patients with Persistent or Transient Congenital Hyperinsulinism.
The Journal of clinical endocrinology and metabolism 2020 3 105 (4): .
Männistö Jonna M E, Maria Maleeha, Raivo Joose, Kuulasmaa Teemu, Otonkoski Timo, Huopio Hanna, Laakso Mark
SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population.
Human genetics 2021 11 141 (1): 81-99.
Mir Ali, Almudhry Montaha, Alghamdi Fouad, Albaradie Raidah, Ibrahim Mona, Aldurayhim Fatimah, Alhedaithy Abdullah, Alamr Mushari, Bawazir Maryam, Mohammad Sahar, Abdelhay Salma, Bashir Shahid, Housawi Yous
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