Jensen H - Search Results

1

Bi-Allelic Pathogenic Variations in MERTK Including Deletions Are Associated with an Early Onset Progressive Form of Retinitis Pigmentosa.

Jespersgaard C, Bertelsen M, Arif F, Gellert-Kristensen HG, Fang M, Jensen H, Rosenberg T, Tümer Z, Møller LB, Brøndum-Nielsen K, Grønskov K. Jespersgaard C, et al. Among authors: jensen h. Genes (Basel). 2020 Dec 18;11(12):1517. doi: 10.3390/genes11121517. Genes (Basel). 2020. PMID: 33353011 Free PMC article.

2

The prevalence and incidence of visual impairment in people of age 20-59 years in industrialized countries: a review.

Rothe Nissen K, Sjølie AK, Jensen H, Borch-Johnsen K, Rosenberg T. Rothe Nissen K, et al. Among authors: jensen h. Ophthalmic Epidemiol. 2003 Oct;10(4):279-91. doi: 10.1076/opep.10.4.279.15909. Ophthalmic Epidemiol. 2003. PMID: 14628970 Review.

3

Blepharophimosis, corneal vascularization, deafness, and acroosteolysis: a "new" syndrome?

Warburg M, Ullman S, Jensen H, Pedersen H, Kobayashi T, Russell B, Tranebjaerg L, Richard G, Brøndum-Nielsen K. Warburg M, et al. Among authors: jensen h. Am J Med Genet A. 2006 Dec 15;140(24):2709-13. doi: 10.1002/ajmg.a.31543. Am J Med Genet A. 2006. PMID: 17103436

4

Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects.

Cingöz S, Bache I, Bjerglund L, Ropers HH, Tommerup N, Jensen H, Brøndum-Nielsen K, Tümer Z. Cingöz S, et al. Among authors: jensen h. Am J Med Genet A. 2011 Jan;155A(1):203-6. doi: 10.1002/ajmg.a.33766. Am J Med Genet A. 2011. PMID: 21204233

5

[The genetic background for the eye malformations anophthalmia and microphthalmia].

Roos LS, Grønskov K, Jensen H, Tümer Z. Roos LS, et al. Among authors: jensen h. Ugeskr Laeger. 2012 Mar 12;174(11):713-6. Ugeskr Laeger. 2012. PMID: 22409892 Danish.

6

Prevalence and diagnostic spectrum of generalized retinal dystrophy in Danish children.

Bertelsen M, Jensen H, Larsen M, Lorenz B, Preising MN, Rosenberg T. Bertelsen M, et al. Among authors: jensen h. Ophthalmic Epidemiol. 2013 Jun;20(3):164-9. doi: 10.3109/09286586.2013.776692. Epub 2013 May 10. Ophthalmic Epidemiol. 2013. PMID: 23662838

7

[Genetic testing and counselling in inherited eye disease].

Brøndum-Nielsen K, Jensen H, Timshel S, Grønskov K, Larsen M. Brøndum-Nielsen K, et al. Among authors: jensen h. Ugeskr Laeger. 2013 Sep 2;175(36):2031-4. Ugeskr Laeger. 2013. PMID: 23992910 Review. Danish.

8

A homozygous mutation in a consanguineous family consolidates the role of ALDH1A3 in autosomal recessive microphthalmia.

Roos L, Fang M, Dali C, Jensen H, Christoffersen N, Wu B, Zhang J, Xu R, Harris P, Xu X, Grønskov K, Tümer Z. Roos L, et al. Among authors: jensen h. Clin Genet. 2014 Sep;86(3):276-81. doi: 10.1111/cge.12277. Epub 2013 Oct 25. Clin Genet. 2014. PMID: 24024553

9

Prevalence of generalized retinal dystrophy in Denmark.

Bertelsen M, Jensen H, Bregnhøj JF, Rosenberg T. Bertelsen M, et al. Among authors: jensen h. Ophthalmic Epidemiol. 2014 Aug;21(4):217-23. doi: 10.3109/09286586.2014.929710. Epub 2014 Jun 25. Ophthalmic Epidemiol. 2014. PMID: 24963760

10

Partial USH2A deletions contribute to Usher syndrome in Denmark.

Dad S, Rendtorff ND, Kann E, Albrechtsen A, Mehrjouy MM, Bak M, Tommerup N, Tranebjærg L, Rosenberg T, Jensen H, Møller LB. Dad S, et al. Among authors: jensen h. Eur J Hum Genet. 2015 Dec;23(12):1646-51. doi: 10.1038/ejhg.2015.54. Epub 2015 Mar 25. Eur J Hum Genet. 2015. PMID: 25804404 Free PMC article.

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