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Fingerprint Dive into the research topics where Jakob Høgild Langdahl is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 15 Similar Profiles
Mutation Medicine & Life Sciences
antineoplaston A10 Medicine & Life Sciences
Point Mutation Medicine & Life Sciences
Bone Density Medicine & Life Sciences
Insulin Resistance Medicine & Life Sciences
Case-Control Studies Medicine & Life Sciences
Glucose Tolerance Test Medicine & Life Sciences
Insulin Medicine & Life Sciences

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Research Output 2014 2019

  • 4 Journal article
  • 2 Poster
  • 1 Ph.D. thesis
  • 1 Comment/debate
39 Downloads (Pure)

Mitochondrial mutation m.3243A>G associates with insulin resistance in non-diabetic carriers.

Langdahl, J. H., Frederiksen, A. L., Vissing, J., Frost, M., Yderstræde, K. B. & Andersen, P. H., Jun 2019, In : Endocrine Connections. 8, 7, p. 829–837

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
Insulin Resistance
Glucose Tolerance Test
Insulin
Mutation
Fat Body

Genetic and endocrine studies of a cohort of m.3243A>G carriers

Langdahl, J. H., 2018, Odense: Syddansk Universitet. Det Sundhedsvidenskabelige Fakultet.

Research output: Book/anthology/thesis/reportPh.D. thesisResearch

71 Downloads (Pure)

Lecocytes mutation load declines with age in carriers of the m.3243A>G mutation: A 10-year Prospective Cohort

Langdahl, J. H., Larsen, M., Frost, M., Andersen, P. H., Yderstraede, K. B., Vissing, J., Dunø, M., Thomassen, M. & Frederiksen, A. L., Apr 2018, In : Clinical Genetics. 93, 4, p. 925-928

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
antineoplaston A10
Mutation
Longitudinal Studies

Boucher Neuhäuser Syndrome - A rare cause of inherited hypogonadotropic hypogonadism: A case of two adult siblings with two novel mutations in PNPLA6

Langdahl, J. H., Frederiksen, A. L., Nguyen, N. N. T. T., Brusgaard, K. & Juhl, C. B., 2017, In : European Journal of Medical Genetics. 60, 2, p. 105-109

Research output: Contribution to journalJournal articleResearchpeer-review

81 Downloads (Pure)

Mitochondrial point mutation m.3243A > G associates with lower bone mineral density, thinner cortices and reduced bone strength: A case-control study

Langdahl, J. H., Frederiksen, A. L., Hansen, S. J., Andersen, P. H., Yderstraede, K. B., Dunø, M., Vissing, J. & Frost, M., 2017, In : Journal of Bone and Mineral Research. 32, 10, p. 2041–2048

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
Point Mutation
Bone Density
Case-Control Studies
Premature Aging
Mutation

Activities 2015 2015

  • 1 Conference presentations

Mitochondrial DNA Point Mutation is Associated with Lower Bone Mineral Density and Altered Bone Structure in a Matched Case-Control Study

Jakob Høgild Langdahl (Guest lecturer), Anja Lisbeth Frederiksen (Guest lecturer), Stinus Hansen (Guest lecturer), Per Heden Andersen (Guest lecturer), Knud Bonnet Yderstræde (Guest lecturer), Morten Dunø (Guest lecturer), John Vissing (Guest lecturer), Morten Frost (Guest lecturer)
26. Apr 2015

Activity: Talks and presentationsConference presentations