Anna Lindstrand

Education:

Karolinska Institute (1999)

Stockholm, Sweden

M.D. - Medicine

Karolinska Institute (2010)

Stockholm, Sweden

Ph.D. - Medical Genetics

Research Interests:

Copy Number Variation

Genetic causes of Mental Retardation

Ciliary Disorders

Selected Publications:

Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes.

Bruno DL, Anderlid BM, Lindstrand A, van Ravenswaaij-Arts C, Ganesamoorthy D, Lundin J, Martin CL, Douglas J, Nowak C, Adam MP, Kooy RF, Van der Aa N, Reyniers E, Vandeweyer G, Stolte-Dijkstra I, Dijkhuizen T, Yeung A, Delatycki M, Borgström B, Thelin L, Cardoso C, van Bon B, Pfundt R, de Vries BB, Wallin A, Amor DJ, James PA, Slater HR, Schoumans J.

J Med Genet. 2010 May;47(5):299-311.

Molecular and clinical characterization of patients with overlapping 10p deletions.

Lindstrand A, Malmgren H, Verri A, Benetti E, Eriksson M, Nordgren A, Anderlid BM, Golovleva I, Schoumans J, Blennow E.

Am J Med Genet A. 2010 May;152A(5):1233-43.

Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH.

Lindstrand A, Schoumans J, Gustavsson P, Hanemaaijer N, Malmgren H, Blennow E.

Clin Genet. 2010 Jun;77(6):552-62. Epub 2010 Mar 4.

Detailed molecular and clinical characterization of three patients with 21q deletions.

Lindstrand A, Malmgren H, Sahlén S, Schoumans J, Nordgren A, Ergander U, Holm E, Anderlid BM, Blennow E.

Clin Genet. 2010 Feb;77(2):145-54. Epub 2009 Oct 23.

Molecular cytogenetic characterization of a constitutional, highly complex intrachromosomal rearrangement of chromosome 1, with 14 breakpoints and a 0.5 Mb submicroscopic deletion.

Lindstrand A, Malmgren H, Sahlén S, Xin H, Schoumans J, Blennow E.