11. Amyotrophic lateral sclerosis in the Faroe Islands – a genealogical study. Issue 7 (2nd October 2021) Authors: Johansen, Malan; Svenstrup, Kirsten; Mortensen, Ólavur; Andorsdóttir, Guðrið; Á Steig, Bjarni; Joensen, Poul; Hansen, Torben; Petersen, Maria Skaalum Journal: Amyotrophic lateral sclerosis and frontotemporal degeneration Issue: Volume 22:Issue 7/8(2021) Page Start: 571 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Archaic Adaptive Introgression in TBX15/WARS2. (22nd December 2016) Authors: Racimo, Fernando; Gokhman, David; Fumagalli, Matteo; Ko, Amy; Hansen, Torben; Moltke, Ida; Albrechtsen, Anders; Carmel, Liran; Huerta-Sánchez, Emilia; Nielsen, Rasmus Journal: Molecular biology and evolution Issue: Volume 34:Number 3(2017:Mar.) Page Start: 509 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Association of alcohol consumption with allergic disease and asthma: a multi‐centre Mendelian randomization analysis*. (30th October 2018) Authors: Skaaby, Tea; Kilpeläinen, Tuomas O.; Taylor, Amy E.; Mahendran, Yuvaraj; Wong, Andrew; Ahluwalia, Tarunveer S.; Paternoster, Lavinia; Trompet, Stella; Stott, David J.; Flexeder, Claudia; Zhou, Ang; Brusselle, Guy; Sajjad, Ayesha; Lahousse, Lies; Tiemeier, Henning; Have, Christian Theil; Thuesen, ... Journal: Addiction Issue: Volume 114:Number 2(2019) Page Start: 216 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. Atorvastatin for prevention of disease progression and hospitalisation in liver cirrhosis: protocol for a randomised, double-blind, placebo-controlled trial. Issue 1 (23rd January 2020) Authors: Kimer, Nina; Grønbæk, Henning; Fred, Rikard Gøran; Hansen, Torben; Deshmukh, Atul Shahaji; Mann, Mathias; Bendtsen, Flemming Journal: BMJ open Issue: Volume 10:Issue 1(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Binge drinking induces an acute burst of markers of hepatic fibrogenesis (PRO‐C3). (10th December 2021) Authors: Torp, Nikolaj; Israelsen, Mads; Nielsen, Mette J.; Åstrand, Claus P.; Juhl, Pernille; Johansen, Stine; Hansen, Camilla D.; Madsen, Bjørn; Villesen, Ida F.; Leeming, Diana J.; Thiele, Maja; Hansen, Torben; Karsdal, Morten; Krag, Aleksander Journal: Liver international Issue: Volume 42:Number 1(2022) Page Start: 92 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Carriers of a VEGFA enhancer polymorphism selectively binding CHOP/DDIT3 are predisposed to increased circulating levels of thyroid-stimulating hormone. Issue 3 (14th September 2016) Authors: Ahluwalia, Tarunveer Singh; Troelsen, Jesper Thorvald; Balslev-Harder, Marie; Bork-Jensen, Jette; Thuesen, Betina Heinsbæk; Cerqueira, Charlotte; Linneberg, Allan; Grarup, Niels; Pedersen, Oluf; Hansen, Torben; Dalgaard, Louise Torp Journal: Journal of medical genetics Issue: Volume 54:Issue 3(2017) Page Start: 166 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Chronic Mild Hyperglycemia in GCK-MODY Patients Does Not Increase Carotid Intima-Media Thickness. (11th September 2013) Authors: Pruhova, Stepanka; Dusatkova, Petra; Kraml, Pavel J.; Kulich, Michal; Prochazkova, Zdena; Broz, Jan; Zikmund, Jaroslav; Cinek, Ondrej; Andel, Michal; Pedersen, Oluf; Hansen, Torben; Lebl, Jan Other Names: Migdalis Ilias Academic Editor. Journal: International journal of endocrinology Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion. Issue 8 (11th October 2022) Authors: Ullah, Asmat; Shah, Abid Ali; Alluqmani, Majed; Haider, Nighat; Aman, Hasan; Alfadhli, Fatima; Almatrafi, Ahmad M.; Albalawi, Alia M.; Krishin, Jai; Ullah Khan, Fati; Anjam, Bilal Ali; Abdullah, ; Lozano, Elionora Peña; Samad, Abdus; Ahmad, Wasim; Hansen, Torben; Xia, Kun; Basit, Sulman Journal: International journal of developmental neuroscience Issue: Volume 82:Issue 8(2022) Page Start: 788 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval. (May 2018) Authors: Lin, Honghuang; van Setten, Jessica; Smith, Albert V.; Bihlmeyer, Nathan A.; Warren, Helen R.; Brody, Jennifer A.; Radmanesh, Farid; Hall, Leanne; Grarup, Niels; Müller-Nurasyid, Martina; Boutin, Thibaud; Verweij, Niek; Lin, Henry J.; Li-Gao, Ruifang; van den Berg, Marten E.; Marten, Jonathan; We... Journal: Circulation Issue: Volume 11:Number 5(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Common variants in LEPR, IL6, AMD1, and NAMPT do not associate with risk of juvenile and childhood obesity in Danes: a case–control study. Issue 1 (December 2015) Authors: Hollensted, Mette; Ahluwalia, Tarunveer; Have, Christian; Grarup, Niels; Fonvig, Cilius; Nielsen, Tenna; Trier, Cæcilie; Paternoster, Lavinia; Pedersen, Oluf; Holm, Jens-Christian; Sørensen, Thorkild; Hansen, Torben Journal: BMC medical genetics Issue: Volume 16:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗