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Best matches for Sørensen SA[au]:

Adult mouse cortical cell taxonomy revealed by single cell transcriptomics. Tasic B et al. Nat Neurosci. (2016)

A mesoscale connectome of the mouse brain. Oh SW et al. Nature. (2014)

Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation. Harris JA et al. Front Neural Circuits. (2014)

Search results

Items: 1 to 50 of 123

1.

Hierarchical organization of cortical and thalamic connectivity.

Harris JA, Mihalas S, Hirokawa KE, Whitesell JD, Choi H, Bernard A, Bohn P, Caldejon S, Casal L, Cho A, Feiner A, Feng D, Gaudreault N, Gerfen CR, Graddis N, Groblewski PA, Henry AM, Ho A, Howard R, Knox JE, Kuan L, Kuang X, Lecoq J, Lesnar P, Li Y, Luviano J, McConoughey S, Mortrud MT, Naeemi M, Ng L, Oh SW, Ouellette B, Shen E, Sorensen SA, Wakeman W, Wang Q, Wang Y, Williford A, Phillips JW, Jones AR, Koch C, Zeng H.

Nature. 2019 Nov;575(7781):195-202. doi: 10.1038/s41586-019-1716-z. Epub 2019 Oct 30.

PMID:
31666704
2.

Classification of electrophysiological and morphological neuron types in the mouse visual cortex.

Gouwens NW, Sorensen SA, Berg J, Lee C, Jarsky T, Ting J, Sunkin SM, Feng D, Anastassiou CA, Barkan E, Bickley K, Blesie N, Braun T, Brouner K, Budzillo A, Caldejon S, Casper T, Castelli D, Chong P, Crichton K, Cuhaciyan C, Daigle TL, Dalley R, Dee N, Desta T, Ding SL, Dingman S, Doperalski A, Dotson N, Egdorf T, Fisher M, de Frates RA, Garren E, Garwood M, Gary A, Gaudreault N, Godfrey K, Gorham M, Gu H, Habel C, Hadley K, Harrington J, Harris JA, Henry A, Hill D, Josephsen S, Kebede S, Kim L, Kroll M, Lee B, Lemon T, Link KE, Liu X, Long B, Mann R, McGraw M, Mihalas S, Mukora A, Murphy GJ, Ng L, Ngo K, Nguyen TN, Nicovich PR, Oldre A, Park D, Parry S, Perkins J, Potekhina L, Reid D, Robertson M, Sandman D, Schroedter M, Slaughterbeck C, Soler-Llavina G, Sulc J, Szafer A, Tasic B, Taskin N, Teeter C, Thatra N, Tung H, Wakeman W, Williams G, Young R, Zhou Z, Farrell C, Peng H, Hawrylycz MJ, Lein E, Ng L, Arkhipov A, Bernard A, Phillips JW, Zeng H, Koch C.

Nat Neurosci. 2019 Jul;22(7):1182-1195. doi: 10.1038/s41593-019-0417-0. Epub 2019 Jun 17.

PMID:
31209381
3.

Correction: Educational delay and attainment in persons with neurofibromatosis 1 in Denmark.

Doser K, Kenborg L, Andersen EW, Bidstrup PE, Kroyer A, Hove H, Østergaard J, Sørensen SA, Johansen C, Mulvihill J, Winther JF, Dalton SO.

Eur J Hum Genet. 2019 Jun;27(6):994-996. doi: 10.1038/s41431-019-0378-5.

4.

Educational delay and attainment in persons with neurofibromatosis 1 in Denmark.

Doser K, Kenborg L, Andersen EW, Bidstrup PE, Kroyer A, Hove H, Østergaard J, Sørensen SA, Johansen C, Mulvihill J, Winther JF, Dalton SO.

Eur J Hum Genet. 2019 Jun;27(6):857-868. doi: 10.1038/s41431-019-0359-8. Epub 2019 Feb 28. Erratum in: Eur J Hum Genet. 2019 Mar 22;:.

PMID:
30820037
5.

Visual physiology of the layer 4 cortical circuit in silico.

Arkhipov A, Gouwens NW, Billeh YN, Gratiy S, Iyer R, Wei Z, Xu Z, Abbasi-Asl R, Berg J, Buice M, Cain N, da Costa N, de Vries S, Denman D, Durand S, Feng D, Jarsky T, Lecoq J, Lee B, Li L, Mihalas S, Ocker GK, Olsen SR, Reid RC, Soler-Llavina G, Sorensen SA, Wang Q, Waters J, Scanziani M, Koch C.

PLoS Comput Biol. 2018 Nov 12;14(11):e1006535. doi: 10.1371/journal.pcbi.1006535. eCollection 2018 Nov.

6.

[Psychiatric symptoms in patients with Huntington's disease].

Jensen RN, Bolwig T, Sørensen SA.

Ugeskr Laeger. 2018 Mar 26;180(13). pii: V07160499. Review. Danish.

PMID:
29587954
7.

Systematic generation of biophysically detailed models for diverse cortical neuron types.

Gouwens NW, Berg J, Feng D, Sorensen SA, Zeng H, Hawrylycz MJ, Koch C, Arkhipov A.

Nat Commun. 2018 Feb 19;9(1):710. doi: 10.1038/s41467-017-02718-3.

8.

The Danish HD Registry-a nationwide family registry of HD families in Denmark.

Gilling M, Budtz-Jørgensen E, Boonen SE, Lildballe D, Bojesen A, Hertz JM, Sørensen SA.

Clin Genet. 2017 Sep;92(3):338-341. doi: 10.1111/cge.12984. Epub 2017 Mar 28.

PMID:
28155235
9.

Adult mouse cortical cell taxonomy revealed by single cell transcriptomics.

Tasic B, Menon V, Nguyen TN, Kim TK, Jarsky T, Yao Z, Levi B, Gray LT, Sorensen SA, Dolbeare T, Bertagnolli D, Goldy J, Shapovalova N, Parry S, Lee C, Smith K, Bernard A, Madisen L, Sunkin SM, Hawrylycz M, Koch C, Zeng H.

Nat Neurosci. 2016 Feb;19(2):335-46. doi: 10.1038/nn.4216. Epub 2016 Jan 4.

10.

Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation.

Harris JA, Hirokawa KE, Sorensen SA, Gu H, Mills M, Ng LL, Bohn P, Mortrud M, Ouellette B, Kidney J, Smith KA, Dang C, Sunkin S, Bernard A, Oh SW, Madisen L, Zeng H.

Front Neural Circuits. 2014 Jul 10;8:76. doi: 10.3389/fncir.2014.00076. eCollection 2014.

11.

Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease.

Petersen MH, Budtz-Jørgensen E, Sørensen SA, Nielsen JE, Hjermind LE, Vinther-Jensen T, Nielsen SM, Nørremølle A.

Mitochondrion. 2014 Jul;17:14-21. doi: 10.1016/j.mito.2014.05.001. Epub 2014 May 15.

PMID:
24836434
12.

A mesoscale connectome of the mouse brain.

Oh SW, Harris JA, Ng L, Winslow B, Cain N, Mihalas S, Wang Q, Lau C, Kuan L, Henry AM, Mortrud MT, Ouellette B, Nguyen TN, Sorensen SA, Slaughterbeck CR, Wakeman W, Li Y, Feng D, Ho A, Nicholas E, Hirokawa KE, Bohn P, Joines KM, Peng H, Hawrylycz MJ, Phillips JW, Hohmann JG, Wohnoutka P, Gerfen CR, Koch C, Bernard A, Dang C, Jones AR, Zeng H.

Nature. 2014 Apr 10;508(7495):207-14. doi: 10.1038/nature13186. Epub 2014 Apr 2.

13.

Correlated gene expression and target specificity demonstrate excitatory projection neuron diversity.

Sorensen SA, Bernard A, Menon V, Royall JJ, Glattfelder KJ, Desta T, Hirokawa K, Mortrud M, Miller JA, Zeng H, Hohmann JG, Jones AR, Lein ES.

Cereb Cortex. 2015 Feb;25(2):433-49. doi: 10.1093/cercor/bht243. Epub 2013 Sep 7.

PMID:
24014670
14.

Relative input strength rapidly regulates dendritic structure of chick auditory brainstem neurons.

Sorensen SA, Rubel EW.

J Comp Neurol. 2011 Oct 1;519(14):2838-51. doi: 10.1002/cne.22656.

15.

Enhanced modern heat transfer to the Arctic by warm Atlantic Water.

Spielhagen RF, Werner K, Sørensen SA, Zamelczyk K, Kandiano E, Budeus G, Husum K, Marchitto TM, Hald M.

Science. 2011 Jan 28;331(6016):450-3. doi: 10.1126/science.1197397.

16.

[Residential institutions or long-term units?].

Sørensen SA.

Ugeskr Laeger. 2010 Mar 1;172(9):731; author reply 731. Danish. No abstract available.

PMID:
20402021
17.

Shifting the paradigm: new approaches for characterizing and classifying neurons.

Bernard A, Sorensen SA, Lein ES.

Curr Opin Neurobiol. 2009 Oct;19(5):530-6. doi: 10.1016/j.conb.2009.09.010. Epub 2009 Nov 5. Review.

PMID:
19896835
18.

4p16.3 haplotype modifying age at onset of Huntington disease.

Nørremølle A, Budtz-Jørgensen E, Fenger K, Nielsen JE, Sørensen SA, Hasholt L.

Clin Genet. 2009 Mar;75(3):244-50. doi: 10.1111/j.1399-0004.2008.01136.x.

PMID:
19250382
19.

Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy.

Schiffmann R, Warnock DG, Banikazemi M, Bultas J, Linthorst GE, Packman S, Sorensen SA, Wilcox WR, Desnick RJ.

Nephrol Dial Transplant. 2009 Jul;24(7):2102-11. doi: 10.1093/ndt/gfp031. Epub 2009 Feb 13.

20.

Osteopenia: a common aspect of Fabry disease. Predictors of bone mineral density.

Mersebach H, Johansson JO, Rasmussen AK, Bengtsson BA, Rosenberg K, Hasholt L, Sørensen SA, Sørensen SS, Feldt-Rasmussen U.

Genet Med. 2007 Dec;9(12):812-8.

PMID:
18091430
21.

Impaired glucose tolerance in the R6/1 transgenic mouse model of Huntington's disease.

Josefsen K, Nielsen MD, Jørgensen KH, Bock T, Nørremølle A, Sørensen SA, Naver B, Hasholt L.

J Neuroendocrinol. 2008 Feb;20(2):165-72. Epub 2007 Nov 22.

PMID:
18034868
22.

High throughput profile-profile based fold recognition for the entire human proteome.

McGuffin LJ, Smith RT, Bryson K, Sørensen SA, Jones DT.

BMC Bioinformatics. 2006 Jun 7;7:288.

23.

The level and integrity of synaptic input regulates dendrite structure.

Sorensen SA, Rubel EW.

J Neurosci. 2006 Feb 1;26(5):1539-50.

24.

Dopa-responsive dystonia and early-onset Parkinson's disease in a patient with GTP cyclohydrolase I deficiency?

Hjermind LE, Johannsen LG, Blau N, Wevers RA, Lucking CB, Hertz JM, Friberg L, Regeur L, Nielsen JE, Sørensen SA.

Mov Disord. 2006 May;21(5):679-82.

PMID:
16267845
25.

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia.

Skibinski G, Parkinson NJ, Brown JM, Chakrabarti L, Lloyd SL, Hummerich H, Nielsen JE, Hodges JR, Spillantini MG, Thusgaard T, Brandner S, Brun A, Rossor MN, Gade A, Johannsen P, Sørensen SA, Gydesen S, Fisher EM, Collinge J.

Nat Genet. 2005 Aug;37(8):806-8. Epub 2005 Jul 24.

PMID:
16041373
26.

Reduced regional cerebral blood flow in SPG4-linked hereditary spastic paraplegia.

Scheuer KH, Nielsen JE, Krabbe K, Simonsen C, Koefoed P, Sørensen SA, Gade A, Paulson OB, Law I.

J Neurol Sci. 2005 Aug 15;235(1-2):23-32.

PMID:
15939438
27.

Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.

Nielsen JE, Johnsen B, Koefoed P, Scheuer KH, Grønbech-Jensen M, Law I, Krabbe K, Nørremølle A, Eiberg H, Søndergård H, Dam M, Rehfeld JF, Krarup C, Paulson OB, Hasholt L, Sørensen SA.

Eur J Neurol. 2004 Dec;11(12):817-24.

PMID:
15667412
28.

Mosaicism of the CAG repeat sequence in the Huntington disease gene in a pair of monozygotic twins.

Nørremølle A, Hasholt L, Petersen CB, Eiberg H, Hasselbalch SG, Gideon P, Nielsen JE, Sørensen SA.

Am J Med Genet A. 2004 Oct 1;130A(2):154-9.

PMID:
15372528
29.

The genomic threading database.

McGuffin LJ, Street S, Sørensen SA, Jones DT.

Bioinformatics. 2004 Jan 1;20(1):131-2.

PMID:
14693823
30.

The Genomic Threading Database: a comprehensive resource for structural annotations of the genomes from key organisms.

McGuffin LJ, Street SA, Bryson K, Sørensen SA, Jones DT.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D196-9.

31.

Molecular and behavioral analysis of the R6/1 Huntington's disease transgenic mouse.

Naver B, Stub C, Møller M, Fenger K, Hansen AK, Hasholt L, Sørensen SA.

Neuroscience. 2003;122(4):1049-57.

PMID:
14643771
32.
33.

Antisense downregulation of mutant huntingtin in a cell model.

Hasholt L, Abell K, Nørremølle A, Nellemann C, Fenger K, Sørensen SA.

J Gene Med. 2003 Jun;5(6):528-38.

PMID:
12797118
34.

A novel mutation in the epsilon-sarcoglycan gene causing myoclonus-dystonia syndrome.

Hjermind LE, Werdelin LM, Eiberg H, Krag-Olsen B, Dupont E, Sørensen SA.

Neurology. 2003 May 13;60(9):1536-9.

PMID:
12743249
35.
36.

Chromosome 3 linked frontotemporal dementia (FTD-3).

Gydesen S, Brown JM, Brun A, Chakrabarti L, Gade A, Johannsen P, Rossor M, Thusgaard T, Grove A, Yancopoulou D, Spillantini MG, Fisher EM, Collinge J, Sorensen SA.

Neurology. 2002 Nov 26;59(10):1585-94.

PMID:
12451202
37.

Fabry disease--a metabolic disorder with a challenge for endocrinologists?

Feldt-Rasmussen U, Rasmussen AK, Mersebach H, Rosenberg KM, Hasholt L, Sorensen SA.

Horm Res. 2002;58(6):259-65. Review.

PMID:
12446988
38.

Fabry disease: a new challenge in endocrinology and metabolism?

Feldt-Rasmussen U, Rasmussen AK, Mersebach H, Rosenberg KM, Hasholt L, Sorensen SA.

Eur J Endocrinol. 2002 Jun;146(6):741-2. Review. No abstract available.

PMID:
12039692
39.

Inherited and de novo mutations in sporadic cases of DYT1-dystonia.

Hjermind LE, Werdelin LM, Sørensen SA.

Eur J Hum Genet. 2002 Mar;10(3):213-6.

40.

[Fabry disease--a special therapy now available].

Rasmussen AK, Mersebach H, Hasholt L, Rosenberg KM, Sørensen SA, Feldt-Rasmussen UF.

Ugeskr Laeger. 2001 Sep 24;163(39):5382. Danish. No abstract available.

PMID:
11590956
41.

Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world.

Lund A, Udd B, Juvonen V, Andersen PM, Cederquist K, Davis M, Gellera C, Kölmel C, Ronnevi LO, Sperfeld AD, Sörensen SA, Tranebjaerg L, Van Maldergem L, Watanabe M, Weber M, Yeung L, Savontaus ML.

Eur J Hum Genet. 2001 Jun;9(6):431-6.

42.

Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p.

Nielsen JE, Jennum P, Fenger K, Sørensen SA, Fuglsang-Frederiksen A.

Eur J Neurol. 2001 Jul;8(4):335-9.

PMID:
11422430
43.

Benzodiazepine receptor quantification in Huntington's disease with [(123)I]omazenil and SPECT.

Pinborg LH, Videbaek C, Hasselbalch SG, Sørensen SA, Wagner A, Paulson OB, Knudsen GM.

J Neurol Neurosurg Psychiatry. 2001 May;70(5):657-61.

44.

Platelet serotonin transporters and the transporter gene in control subjects, unipolar patients and bipolar patients.

Mellerup E, Bennike B, Bolwig T, Dam H, Hasholt L, Jørgensen MB, Plenge P, Sørensen SA.

Acta Psychiatr Scand. 2001 Mar;103(3):229-33.

PMID:
11240581
45.

Inhibition of Huntington synthesis by antisense oligodeoxynucleotides.

Nellemann C, Abell K, Nørremølle A, Løkkegaard T, Naver B, Röpke C, Rygaard J, Sørensen SA, Hasholt L.

Mol Cell Neurosci. 2000 Oct;16(4):313-23.

PMID:
11085870
46.

[Hereditary dystonias].

Hjermind LE, Sørensen SA, Werdelin LM.

Ugeskr Laeger. 2000 Sep 18;162(38):5066-70. Review. Danish.

PMID:
11014135
47.

[Preimplantation diagnosis of dominant inherited diseases with late debut].

Sørensen SA.

Ugeskr Laeger. 2000 Aug 14;162(33):4371-3. Danish. No abstract available.

PMID:
10962958
48.

Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia.

Lund A, Udd B, Juvonen V, Andersen PM, Cederquist K, Ronnevi LO, Sistonen P, Sörensen SA, Tranebjaerg L, Wallgren-Pettersson C, Savontaus ML.

Eur J Hum Genet. 2000 Aug;8(8):631-6.

49.

[Molecular biology and genetic counseling].

Sørensen SA.

Ugeskr Laeger. 2000 Mar 13;162(11):1574-5. Danish. No abstract available.

PMID:
10868119
50.

Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2.

Larsen LA, Svendsen IH, Jensen AM, Kanters JK, Andersen PS, Møller M, Sørensen SA, Sandøe E, Jacobsen JR, Vuust J, Christiansen M.

Clin Genet. 2000 Feb;57(2):125-30.

PMID:
10735633

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