| Year |
Citation |
Score |
| 2023 |
Sorensen SA, Gouwens NW, Wang Y, Mallory M, Budzillo A, Dalley R, Lee B, Gliko O, Kuo HC, Kuang X, Mann R, Ahmadinia L, Alfiler L, Baftizadeh F, Baker K, et al. Connecting single-cell transcriptomes to projectomes in mouse visual cortex. Biorxiv : the Preprint Server For Biology. PMID 38168270 DOI: 10.1101/2023.11.25.568393 |
0.55 |
|
| 2023 |
Lee BR, Dalley R, Miller JA, Chartrand T, Close J, Mann R, Mukora A, Ng L, Alfiler L, Baker K, Bertagnolli D, Brouner K, Casper T, Csajbok E, Donadio N, ... ... Sorensen SA, et al. Signature morphoelectric properties of diverse GABAergic interneurons in the human neocortex. Science (New York, N.Y.). 382: eadf6484. PMID 37824669 DOI: 10.1126/science.adf6484 |
0.504 |
|
| 2023 |
Gabitto M, Travaglini K, Ariza J, Kaplan E, Long B, Rachleff V, Ding Y, Mahoney J, Dee N, Goldy J, Melief E, Brouner K, Compos J, Campos J, Carr A, ... ... Sorensen S, et al. Integrated multimodal cell atlas of Alzheimer's disease. Research Square. PMID 37292694 DOI: 10.21203/rs.3.rs-2921860/v1 |
0.302 |
|
| 2023 |
Kim MH, Radaelli C, Thomsen ER, Monet D, Chartrand T, Jorstad NL, Mahoney JT, Taormina MJ, Long B, Baker K, Bakken TE, Campagnola L, Casper T, Clark M, Dee N, ... ... Sorensen S, et al. Target cell-specific synaptic dynamics of excitatory to inhibitory neuron connections in supragranular layers of human neocortex. Elife. 12. PMID 37249212 DOI: 10.7554/eLife.81863 |
0.465 |
|
| 2023 |
Wang Q, Wang Y, Kuo HC, Xie P, Kuang X, Hirokawa KE, Naeemi M, Yao S, Mallory M, Ouellette B, Lesnar P, Li Y, Ye M, Chen C, Xiong W, ... ... Sorensen SA, et al. Regional and cell-type-specific afferent and efferent projections of the mouse claustrum. Cell Reports. 42: 112118. PMID 36774552 DOI: 10.1016/j.celrep.2023.112118 |
0.647 |
|
| 2022 |
Campagnola L, Seeman SC, Chartrand T, Kim L, Hoggarth A, Gamlin C, Ito S, Trinh J, Davoudian P, Radaelli C, Kim MH, Hage T, Braun T, Alfiler L, Andrade J, ... ... Sorensen S, et al. Local connectivity and synaptic dynamics in mouse and human neocortex. Science (New York, N.Y.). 375: eabj5861. PMID 35271334 DOI: 10.1126/science.abj5861 |
0.465 |
|
| 2022 |
Berg J, Sorensen SA, Ting JT, Miller JA, Chartrand T, Buchin A, Bakken TE, Budzillo A, Dee N, Ding SL, Gouwens NW, Hodge RD, Kalmbach B, Lee C, Lee BR, et al. Author Correction: Human neocortical expansion involves glutamatergic neuron diversification. Nature. PMID 34992294 DOI: 10.1038/s41586-021-04322-4 |
0.533 |
|
| 2021 |
Peng H, Xie P, Liu L, Kuang X, Wang Y, Qu L, Gong H, Jiang S, Li A, Ruan Z, Ding L, Yao Z, Chen C, Chen M, Daigle TL, ... ... Sorensen SA, et al. Morphological diversity of single neurons in molecularly defined cell types. Nature. 598: 174-181. PMID 34616072 DOI: 10.1038/s41586-021-03941-1 |
0.641 |
|
| 2021 |
Berg J, Sorensen SA, Ting JT, Miller JA, Chartrand T, Buchin A, Bakken TE, Budzillo A, Dee N, Ding SL, Gouwens NW, Hodge RD, Kalmbach B, Lee C, Lee BR, et al. Human neocortical expansion involves glutamatergic neuron diversification. Nature. 598: 151-158. PMID 34616067 DOI: 10.1038/s41586-021-03813-8 |
0.606 |
|
| 2021 |
Bakken TE, Jorstad NL, Hu Q, Lake BB, Tian W, Kalmbach BE, Crow M, Hodge RD, Krienen FM, Sorensen SA, Eggermont J, Yao Z, Aevermann BD, Aldridge AI, Bartlett A, et al. Comparative cellular analysis of motor cortex in human, marmoset and mouse. Nature. 598: 111-119. PMID 34616062 DOI: 10.1038/s41586-021-03465-8 |
0.373 |
|
| 2021 |
Kalmbach BE, Hodge RD, Jorstad NL, Owen S, de Frates R, Yanny AM, Dalley R, Mallory M, Graybuck LT, Radaelli C, Keene CD, Gwinn RP, Silbergeld DL, Cobbs C, Ojemann JG, ... ... Sorensen SA, et al. Signature morpho-electric, transcriptomic, and dendritic properties of human layer 5 neocortical pyramidal neurons. Neuron. 109: 2914-2927.e5. PMID 34534454 DOI: 10.1016/j.neuron.2021.08.030 |
0.409 |
|
| 2020 |
Gouwens NW, Sorensen SA, Baftizadeh F, Budzillo A, Lee BR, Jarsky T, Alfiler L, Baker K, Barkan E, Berry K, Bertagnolli D, Bickley K, Bomben J, Braun T, Brouner K, et al. Integrated Morphoelectric and Transcriptomic Classification of Cortical GABAergic Cells. Cell. 183: 935-953.e19. PMID 33186530 DOI: 10.1016/j.cell.2020.09.057 |
0.47 |
|
| 2019 |
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, ... ... Sorensen SA, et al. Hierarchical organization of cortical and thalamic connectivity. Nature. PMID 31666704 DOI: 10.1038/S41586-019-1716-Z |
0.65 |
|
| 2019 |
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, et al. Classification of electrophysiological and morphological neuron types in the mouse visual cortex. Nature Neuroscience. PMID 31209381 DOI: 10.1038/S41593-019-0417-0 |
0.583 |
|
| 2018 |
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, ... ... Sorensen SA, et al. Visual physiology of the layer 4 cortical circuit in silico. Plos Computational Biology. 14: e1006535. PMID 30419013 DOI: 10.1371/Journal.Pcbi.1006535 |
0.425 |
|
| 2018 |
Gouwens NW, Berg J, Feng D, Sorensen SA, Zeng H, Hawrylycz MJ, Koch C, Arkhipov A. Systematic generation of biophysically detailed models for diverse cortical neuron types. Nature Communications. 9: 710. PMID 29459718 DOI: 10.1038/S41467-017-02718-3 |
0.478 |
|
| 2016 |
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, et al. Adult mouse cortical cell taxonomy revealed by single cell transcriptomics. Nature Neuroscience. PMID 26727548 DOI: 10.1038/Nn.4216 |
0.621 |
|
| 2015 |
Zhou Z, Sorensen S, Zeng H, Hawrylycz M, Peng H. Adaptive Image Enhancement for Tracing 3D Morphologies of Neurons and Brain Vasculatures. Neuroinformatics. 13: 153-66. PMID 25310965 DOI: 10.1007/S12021-014-9249-Y |
0.425 |
|
| 2015 |
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. Correlated gene expression and target specificity demonstrate excitatory projection neuron diversity. Cerebral Cortex (New York, N.Y. : 1991). 25: 433-49. PMID 24014670 DOI: 10.1093/Cercor/Bht243 |
0.573 |
|
| 2015 |
Zhou Z, Sorensen SA, Peng H. Neuron crawler: An automatic tracing algorithm for very large neuron images Proceedings - International Symposium On Biomedical Imaging. 2015: 870-874. DOI: 10.1109/ISBI.2015.7164009 |
0.338 |
|
| 2014 |
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, et al. Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation. Frontiers in Neural Circuits. 8: 76. PMID 25071457 DOI: 10.3389/Fncir.2014.00076 |
0.627 |
|
| 2014 |
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, et al. A mesoscale connectome of the mouse brain. Nature. 508: 207-14. PMID 24695228 DOI: 10.1038/Nature13186 |
0.608 |
|
| 2011 |
Sorensen SA, Rubel EW. Relative input strength rapidly regulates dendritic structure of chick auditory brainstem neurons. The Journal of Comparative Neurology. 519: 2838-51. PMID 21500196 DOI: 10.1002/cne.22656 |
0.578 |
|
| 2009 |
Bernard A, Sorensen SA, Lein ES. Shifting the paradigm: new approaches for characterizing and classifying neurons. Current Opinion in Neurobiology. 19: 530-6. PMID 19896835 DOI: 10.1016/j.conb.2009.09.010 |
0.578 |
|
| 2006 |
Sorensen SA, Rubel EW. The level and integrity of synaptic input regulates dendrite structure. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 1539-50. PMID 16452677 DOI: 10.1523/JNEUROSCI.3807-05.2006 |
0.49 |
|
| 1996 |
Yanagisawa H, Fujii K, Nagafuchi S, Nakahori Y, Nakagome Y, Akane A, Nakamura M, Sano A, Komure O, Kondo I, Jin DK, Sørensen SA, Potter NT, Young SR, Nakamura K, et al. A unique origin and multistep process for the generation of expanded DRPLA triplet repeats. Human Molecular Genetics. 5: 373-9. PMID 8852663 DOI: 10.1093/Hmg/5.3.373 |
0.41 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2021 |
Lee BR, Budzillo A, Hadley K, Miller JA, Jarsky T, Baker K, Hill D, Kim L, Mann R, Ng L, Oldre A, Rajanbabu R, Trinh J, Vargas S, Braun T, ... ... Sorensen S, et al. Scaled, high fidelity electrophysiological, morphological, and transcriptomic cell characterization. Elife. 10. PMID 34387544 DOI: 10.7554/eLife.65482 |
0.283 |
|
| 2023 |
Chartrand T, Dalley R, Close J, Goriounova NA, Lee BR, Mann R, Miller JA, Molnar G, Mukora A, Alfiler L, Baker K, Bakken TE, Berg J, Bertagnolli D, Braun T, ... ... Sorensen SA, et al. Morphoelectric and transcriptomic divergence of the layer 1 interneuron repertoire in human versus mouse neocortex. Science (New York, N.Y.). 382: eadf0805. PMID 37824667 DOI: 10.1126/science.adf0805 |
0.236 |
|
| 2005 |
Scheuer KH, Nielsen JE, Krabbe K, Simonsen C, Koefoed P, Sørensen SA, Gade A, Paulson OB, Law I. Reduced regional cerebral blood flow in SPG4-linked hereditary spastic paraplegia. Journal of the Neurological Sciences. 235: 23-32. PMID 15939438 DOI: 10.1016/J.Jns.2005.03.051 |
0.209 |
|
| 2002 |
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. Chromosome 3 linked frontotemporal dementia (FTD-3). Neurology. 59: 1585-94. PMID 12451202 DOI: 10.1212/01.Wnl.0000034763.54161.1F |
0.193 |
|
| 1998 |
Koefoed P, Hasholt L, Fenger K, Nielsen JE, Eiberg H, Buschard K, Sørensen SA. Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1. Human Genetics. 103: 564-9. PMID 9860298 |
0.189 |
|
| 2001 |
Pinborg LH, Videbaek C, Hasselbalch SG, Sørensen SA, Wagner A, Paulson OB, Knudsen GM. Benzodiazepine receptor quantification in Huntington's disease with [(123)I]omazenil and SPECT. Journal of Neurology, Neurosurgery, and Psychiatry. 70: 657-61. PMID 11309461 DOI: 10.1136/Jnnp.70.5.657 |
0.187 |
|
| 2003 |
Sorensen SA, Jones TA, Olavarria JF. Neonatal enucleation reduces the proportion of callosal boutons forming multiple synaptic contacts in rat striate cortex. Neuroscience Letters. 351: 17-20. PMID 14550903 DOI: 10.1016/S0304-3940(03)00938-8 |
0.177 |
|
| 1992 |
Mouridsen SE, Andersen LB, Sörensen SA, Rich B, Isager T. Neurofibromatosis in infantile autism and other types of childhood psychoses. Acta Paedopsychiatrica. 55: 15-8. PMID 1310363 |
0.172 |
|
| 2003 |
Hasholt L, Abell K, Nørremølle A, Nellemann C, Fenger K, Sørensen SA. Antisense downregulation of mutant huntingtin in a cell model. The Journal of Gene Medicine. 5: 528-38. PMID 12797118 DOI: 10.1002/jgm.378 |
0.159 |
|
| 2022 |
Bakken TE, Jorstad NL, Hu Q, Lake BB, Tian W, Kalmbach BE, Crow M, Hodge RD, Krienen FM, Sorensen SA, Eggermont J, Yao Z, Aevermann BD, Aldridge AI, Bartlett A, et al. Author Correction: Comparative cellular analysis of motor cortex in human, marmoset and mouse. Nature. PMID 35319013 DOI: 10.1038/s41586-022-04562-y |
0.152 |
|
| 2008 |
Josefsen K, Nielsen MD, Jørgensen KH, Bock T, Nørremølle A, Sørensen SA, Naver B, Hasholt L. Impaired glucose tolerance in the R6/1 transgenic mouse model of Huntington's disease. Journal of Neuroendocrinology. 20: 165-72. PMID 18034868 DOI: 10.1111/j.1365-2826.2007.01629.x |
0.147 |
|
| 2022 |
Buchin A, de Frates R, Nandi A, Mann R, Chong P, Ng L, Miller J, Hodge R, Kalmbach B, Bose S, Rutishauser U, McConoughey S, Lein E, Berg J, Sorensen S, et al. Multi-modal characterization and simulation of human epileptic circuitry. Cell Reports. 41: 111873. PMID 36577383 DOI: 10.1016/j.celrep.2022.111873 |
0.143 |
|
| 1975 |
Sorensen SA. Report and characterization of a new variant, EB, of human red cell acid phosphatase. American Journal of Human Genetics. 27: 100-9. PMID 239593 |
0.131 |
|
| 1972 |
Sorensen SA. Zymograms of the human red cell acid phosphatase obtained with different substrates. Clinical Genetics. 3: 483-9. PMID 4650867 |
0.127 |
|
| 1992 |
Hasselbalch SG, Oberg G, Sørensen SA, Andersen AR, Waldemar G, Schmidt JF, Fenger K, Paulson OB. Reduced regional cerebral blood flow in Huntington's disease studied by SPECT. Journal of Neurology, Neurosurgery, and Psychiatry. 55: 1018-23. PMID 1469396 DOI: 10.1136/Jnnp.55.11.1018 |
0.123 |
|
| 1974 |
Sørensen SA. Isoelectric focusing of human red cell acid phosphatase isozymes. Biochemical Genetics. 12: 345-58. PMID 4461032 |
0.12 |
|
| 1999 |
Ashworth A, Lloyd S, Brown J, Gydesen S, Sorensen SA, Brun A, Englund E, Humphreys C, Housman D, Badura M, Stanton V, Taylor K, Cameron J, Munroe D, Johansson J, et al. Molecular genetic characterisation of frontotemporal dementia on chromosome 3. Dementia and Geriatric Cognitive Disorders. 10: 93-101. PMID 10436350 DOI: 10.1159/000051222 |
0.116 |
|
| 1993 |
Brown J, Gydesen S, Sorensen SA, Brun A, Smith S, Houlden H, Twells R, Mullan M, Rossor M, Collinge J. Genetic characterization of a familial non-specific dementia originating in Jutland, Denmark. Journal of the Neurological Sciences. 114: 138-43. PMID 8445394 DOI: 10.1016/0022-510X(93)90288-A |
0.116 |
|
| 1974 |
Sorensen SA. Agarose gel electrophoresis of the human red cell acid phosphatase. Vox Sanguinis. 27: 556-63. PMID 4141816 |
0.111 |
|
| 2004 |
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, et al. Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 11: 817-24. PMID 15667412 DOI: 10.1111/J.1468-1331.2004.00888.X |
0.109 |
|
| 2006 |
McGuffin LJ, Smith RT, Bryson K, Sørensen SA, Jones DT. High throughput profile-profile based fold recognition for the entire human proteome. Bmc Bioinformatics. 7: 288. PMID 16759376 DOI: 10.1186/1471-2105-7-288 |
0.106 |
|
| 1973 |
Sorensen SA. Human red cell acid phosphatase polymorphism. Population and family studies in Denmark. Human Heredity. 23: 470-81. PMID 4785875 |
0.098 |
|
| 1975 |
Weitkamp LR, Lovrien EW, Olaisen B, Fenger K, Gedde-Dahl T, Sorensen SA, Conneally PM, Bias WB, Ott J. Linkage relations of the loci for the MN blood group and red cell acid phosphatase. Birth Defects Original Article Series. 11: 276-80. PMID 1203495 |
0.086 |
|
| 1975 |
Weitkamp LR, Lovrien EW, Olaisen B, Fenger K, Gedde-Dahl T, Sorensen SA, Conneally PM, Bias WB, Ott J. Linkage relations of the loci for the MN blood group and red cell acid phosphatase. Cytogenetics and Cell Genetics. 14: 446-50. PMID 1192835 DOI: 10.1159/000130403 |
0.086 |
|
| 1993 |
Andrew S, Theilmann J, Almqvist E, Norremolle A, Lucotte G, Anvret M, Sorensen SA, Turpin JC, Hayden MR. DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease. Clinical Genetics. 43: 286-94. PMID 8370147 DOI: 10.1111/J.1399-0004.1993.Tb03820.X |
0.085 |
|
| 2003 |
Naver B, Stub C, Møller M, Fenger K, Hansen AK, Hasholt L, Sørensen SA. Molecular and behavioral analysis of the R6/1 Huntington's disease transgenic mouse. Neuroscience. 122: 1049-57. PMID 14643771 |
0.077 |
|
| 1974 |
Sorensen SA. The polymorphisms of red cell acid phosphatase, phosphoglucomutase, adenosine deaminase, and adenylate kinase in twins. Human Heredity. 24: 236-46. PMID 4373384 |
0.075 |
|
| 1995 |
Ashworth A, Brown J, Gydesen S, Sorensen SA, Rossor MN, Hardy J, Collinge J. Frontal lobe or 'nonspecific' dementias are genetically heterogeneous. Neurology. 45: 1781. PMID 7675248 DOI: 10.1212/Wnl.45.9.1781 |
0.073 |
|
| 1986 |
Hasholt L, Sørensen SA. Lysosomal alpha-galactosidase in endothelial cell cultures established from a Fabry hemizygous and normal umbilical veins. Human Genetics. 72: 72-6. PMID 3002954 |
0.072 |
|
| 1988 |
Hasholt L, Wandall A, Sørensen SA. Enzyme replacement in Fabry endothelial cells and fibroblasts: uptake experiments and electron microscopical studies. Clinical Genetics. 33: 360-71. PMID 2837353 |
0.072 |
|
| 1976 |
Sorensen SA, Fenger K. Gene frequencies and linkage data on EsD in man. Human Heredity. 26: 90-4. PMID 950243 |
0.071 |
|
| 2004 |
Nørremølle A, Hasholt L, Petersen CB, Eiberg H, Hasselbalch SG, Gideon P, Nielsen JE, Sørensen SA. Mosaicism of the CAG repeat sequence in the Huntington disease gene in a pair of monozygotic twins. American Journal of Medical Genetics. Part A. 130: 154-9. PMID 15372528 DOI: 10.1002/ajmg.a.30128 |
0.071 |
|
| 1993 |
Brown J, Gydesen S, Sorensen SA, Brun A, Duff K, Houlden H, Fidani L, Kullkarni S, Cummings J, Goate A. Exclusion mapping in familial non-specific dementia. Dementia (Basel, Switzerland). 4: 163-6. PMID 8401786 DOI: 10.1159/000107317 |
0.07 |
|
| 1989 |
Sørensen SA. [Huntington chorea]. Ugeskrift For Laeger. 151: 43-4. PMID 2521412 |
0.069 |
|
| 1996 |
Madsen KM, Hasholt L, Berger J, Sørensen SA. SSCP analysis of paraffin wax embedded tissues in a family with an atypical form of Fabry disease. Clinical Molecular Pathology. 49: M310-2. PMID 16696095 |
0.067 |
|
| 1983 |
Madsen H, Staub Nielsen L, Sørensen SA. Genetic markers in Huntington's disease. An association study on Danish patients. Hereditas. 99: 305-7. PMID 6230337 |
0.059 |
|
| 1992 |
Nørremølle A, Sørensen SA, Arctander P. Nucleotide sequence and PCR-amplification of a polymorphic MboI site in human DNA marker D4S95 linked to the Huntington disease locus. Clinical Genetics. 42: 210-1. PMID 1358489 |
0.059 |
|
| 1995 |
Nørremølle A, Sørensen SA, Fenger K, Hasholt L. Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease. Clinical Genetics. 47: 113-7. PMID 7634532 |
0.058 |
|
| 2017 |
Gilling M, Budtz-Jørgensen E, Boonen SE, Lildballe D, Bojesen A, Hertz JM, Sørensen SA. The Danish HD Registry-a nationwide family registry of HD families in Denmark. Clinical Genetics. 92: 338-341. PMID 28155235 DOI: 10.1111/cge.12984 |
0.058 |
|
| 2004 |
McGuffin LJ, Street SA, Bryson K, Sørensen SA, Jones DT. The Genomic Threading Database: a comprehensive resource for structural annotations of the genomes from key organisms. Nucleic Acids Research. 32: D196-9. PMID 14681393 DOI: 10.1093/nar/gkh043 |
0.056 |
|
| 1995 |
Rosenberg NK, Sørensen SA, Christensen AL. Neuropsychological characteristics of Huntington's disease carriers: a double blind study. Journal of Medical Genetics. 32: 600-4. PMID 7473650 DOI: 10.1136/jmg.32.8.600 |
0.056 |
|
| 1993 |
Nørremølle A, Riess O, Epplen JT, Fenger K, Hasholt L, Sørensen SA. Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish families. Human Molecular Genetics. 2: 1475-6. PMID 8242074 |
0.055 |
|
| 2000 |
Sørensen SA. [Molecular biology and genetic counseling]. Ugeskrift For Laeger. 162: 1574-5. PMID 10868119 |
0.053 |
|
| 1998 |
Sorensen SA, Low JO. Siting criteria based on the prevention of deterministic effects from plutonium inhalation exposures. Health Physics. 75: 614-8. PMID 9827508 |
0.051 |
|
| 2009 |
Saeedi P, Sorensen SA. Mathematical-based benchmarking: To predict ANT exploration time-series dataset Proceedings - 2009 International Conference On Computational Intelligence and Software Engineering, Cise 2009. DOI: 10.1109/CISE.2009.5366677 |
0.051 |
|
| 1975 |
Fenger K, Sorensen SA. Evaluation of a possible sex difference in recombination for the ABO-AK linkage. American Journal of Human Genetics. 27: 784-8. PMID 173186 |
0.05 |
|
| 1996 |
Nielsen JE, Sørensen SA, Hasholt L, Nørremølle A. Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family. Movement Disorders : Official Journal of the Movement Disorder Society. 11: 533-41. PMID 8866494 DOI: 10.1002/mds.870110508 |
0.05 |
|
| 2003 |
Nørremølle A, Grunnet M, Hasholt L, Sørensen SA. Cells exposed to a huntingtin fragment containing an expanded polyglutamine tract show no sign of ion channel formation: results arguing against the ion channel hypothesis. Journal of Neuroscience Research. 71: 132-7. PMID 12478622 DOI: 10.1002/jnr.10468 |
0.049 |
|
| 1996 |
Madsen KM, Hasholt L, Sørensen SA, van Loo A, Vanholder R. The utility of single-strand conformation polymorphism (SSCP) analysis: results obtained in families with Fabry's disease. Scandinavian Journal of Clinical and Laboratory Investigation. 56: 177-82. PMID 8743111 |
0.049 |
|
| 2006 |
Hjermind LE, Johannsen LG, Blau N, Wevers RA, Lucking CB, Hertz JM, Friberg L, Regeur L, Nielsen JE, Sørensen SA. Dopa-responsive dystonia and early-onset Parkinson's disease in a patient with GTP cyclohydrolase I deficiency? Movement Disorders : Official Journal of the Movement Disorder Society. 21: 679-82. PMID 16267845 DOI: 10.1002/Mds.20773 |
0.049 |
|
| 1993 |
Russell MB, Hilden J, Sørensen SA, Olesen J. Familial occurrence of migraine without aura and migraine with aura. Neurology. 43: 1369-73. PMID 8392151 DOI: 10.1212/Wnl.43.7.1369 |
0.047 |
|
| 1982 |
Madsen H, Nielsen LS, Sørensen SA. An association study of Huntington's disease and HLA. Journal of Medical Genetics. 19: 452-4. PMID 6218304 |
0.047 |
|
| 1995 |
Nørremølle A, Nielsen JE, Sørensen SA, Hasholt L. Elongated CAG repeats of the B37 gene in a Danish family with dentato-rubro-pallido-luysian atrophy. Human Genetics. 95: 313-8. PMID 7868125 |
0.047 |
|
| 2005 |
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, et al. Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nature Genetics. 37: 806-8. PMID 16041373 DOI: 10.1038/Ng1609 |
0.046 |
|
| 1984 |
Hasholt L, Sørensen SA. A microtechnique for quantitative measurements of acid hydrolases in fibroblasts. Its application in diagnosis of Fabry disease and enzyme replacement studies. Clinica Chimica Acta; International Journal of Clinical Chemistry. 142: 257-61. PMID 6094040 |
0.046 |
|
| 1998 |
Nielsen JE, Krabbe K, Jennum P, Koefoed P, Jensen LN, Fenger K, Eiberg H, Hasholt L, Werdelin L, Sørensen SA. Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study. Journal of Neurology, Neurosurgery, and Psychiatry. 64: 61-6. PMID 9436729 |
0.046 |
|
| 1976 |
Cohn J, Hanel HK, Sorensen SA, Warburg M. [Hereditary hemolytic anemia resulting from erythrocyte enzyme defects. Biochemical, genetic and clinical aspects]. Ugeskrift For Laeger. 138: 2372-6. PMID 135388 |
0.045 |
|
| 2002 |
Feldt-Rasmussen U, Rasmussen AK, Mersebach H, Rosenberg KM, Hasholt L, Sorensen SA. Fabry disease: a new challenge in endocrinology and metabolism? European Journal of Endocrinology / European Federation of Endocrine Societies. 146: 741-2. PMID 12039692 |
0.045 |
|
| 2000 |
Rosenberg KM, Schiffmann R, Kaneski C, Brady RO, Sorensen SA, Hasholt L. Five novel mutations in fourteen patients with Fabry Disease. Human Mutation. 15: 207-8. PMID 10649504 DOI: 10.1002/(Sici)1098-1004(200002)15:2<207::Aid-Humu16>3.0.Co;2-C |
0.044 |
|
| 1996 |
Colding-Jørgensen E, Sørensen SA, Hasholt L, Lauritzen M. Electrophysiological findings in a Danish family with Machado-Joseph disease. Muscle & Nerve. 19: 743-50. PMID 8609925 DOI: 10.1002/(SICI)1097-4598(199606)19:6<743::AID-MUS9>3.0.CO;2-A |
0.043 |
|
| 1990 |
Hasholt L, Sørensen SA, Wandall A, Andersen EB, Arlien-Søborg P. A Fabry's disease heterozygote with a new mutation: biochemical, ultrastructural, and clinical investigations. Journal of Medical Genetics. 27: 303-6. PMID 2161929 |
0.043 |
|
| 1989 |
Sørensen SA, Fenger K. Huntington's chorea: general practitioners' knowledge about individuals' at-risk status. Scandinavian Journal of Primary Health Care. 7: 49-52. PMID 2524869 |
0.042 |
|
| 2009 |
Schiffmann R, Warnock DG, Banikazemi M, Bultas J, Linthorst GE, Packman S, Sorensen SA, Wilcox WR, Desnick RJ. Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 24: 2102-11. PMID 19218538 DOI: 10.1093/Ndt/Gfp031 |
0.042 |
|
| 1985 |
Milman N, Graudal N, Nielsen LS, Sørensen SA. HLA determinants in idiopathic haemochromatosis. Danish Medical Bulletin. 32: 262-4. PMID 4053696 |
0.041 |
|
| 1987 |
Gydesen S, Hagen S, Klinken L, Abelskov J, Sørensen SA. Neuropsychiatric studies in a family with presenile dementia different from Alzheimer and Pick disease. Acta Psychiatrica Scandinavica. 76: 276-84. PMID 3673655 |
0.041 |
|
| 1997 |
McMorrow DF, Lussier JG, Lebech B, Sørensen SA, Christensen MJ, Vogt O. X-ray scattering study of the interplay between magnetism and structure in CeSb Journal of Physics Condensed Matter. 9: 1133-1148. DOI: 10.1088/0953-8984/9/5/017 |
0.039 |
|
| 2004 |
McGuffin LJ, Street S, Sørensen SA, Jones DT. The genomic threading database. Bioinformatics (Oxford, England). 20: 131-2. PMID 14693823 |
0.039 |
|
| 2001 |
Nielsen JE, Jennum P, Fenger K, Sørensen SA, Fuglsang-Frederiksen A. Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 8: 335-9. PMID 11422430 |
0.037 |
|
| 2009 |
Saeedi P, Sorensen SA. Mathematical-based benchmarking and performance improvement for ANT exploration algorithm 2009 Ieee International Conference On Robotics and Biomimetics, Robio 2009. 859-864. DOI: 10.1109/ROBIO.2009.5420562 |
0.036 |
|
| 1998 |
Jensen P, Fenger K, Bolwig TG, Sørensen SA. Crime in Huntington's disease: a study of registered offences among patients, relatives, and controls. Journal of Neurology, Neurosurgery, and Psychiatry. 65: 467-71. PMID 9771767 |
0.036 |
|
| 2001 |
Rasmussen AK, Mersebach H, Hasholt L, Rosenberg KM, Sørensen SA, Feldt-Rasmussen UF. [Fabry disease--a special therapy now available]. Ugeskrift For Laeger. 163: 5382. PMID 11590956 |
0.035 |
|
| 1997 |
Nielsen JE, Koefoed P, Abell K, Hasholt L, Eiberg H, Fenger K, Niebuhr E, Sørensen SA. CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24. Human Molecular Genetics. 6: 1811-6. PMID 9302257 |
0.035 |
|
| 1992 |
Sørensen SA, Fenger K. Causes of death in patients with Huntington's disease and in unaffected first degree relatives. Journal of Medical Genetics. 29: 911-4. PMID 1479606 |
0.034 |
|
| 1972 |
Sorensen SA. Adenylate kinase, adenosine deaminase and phosphoglucomutase phenotypes in a Danish population. Human Heredity. 22: 362-71. PMID 4647202 |
0.033 |
|
| 2011 |
Spielhagen RF, Werner K, Sørensen SA, Zamelczyk K, Kandiano E, Budeus G, Husum K, Marchitto TM, Hald M. Enhanced modern heat transfer to the Arctic by warm Atlantic Water. Science (New York, N.Y.). 331: 450-3. PMID 21273485 DOI: 10.1126/Science.1197397 |
0.033 |
|
| 2003 |
Hjermind LE, Werdelin LM, Eiberg H, Krag-Olsen B, Dupont E, Sørensen SA. A novel mutation in the epsilon-sarcoglycan gene causing myoclonus-dystonia syndrome. Neurology. 60: 1536-9. PMID 12743249 |
0.032 |
|
| 2002 |
Feldt-Rasmussen U, Rasmussen AK, Mersebach H, Rosenberg KM, Hasholt L, Sorensen SA. Fabry disease--a metabolic disorder with a challenge for endocrinologists? Hormone Research. 58: 259-65. PMID 12446988 |
0.029 |
|
| 2002 |
Feldt-Rasmussen U, Rasmussen AK, Mersebach H, Rosenberg KM, Hasholt L, Sorensen SA. Fabry disease - A metabolic disorder with a challenge for endocrinologists? Hormone Research. 58: 259-265. DOI: 10.1159/000066443 |
0.029 |
|
| 1999 |
Sørensen SA, Fenger K, Olsen JH. Significantly lower incidence of cancer among patients with Huntington disease: An apoptotic effect of an expanded polyglutamine tract? Cancer. 86: 1342-6. PMID 10506723 DOI: 10.1002/(SICI)1097-0142(19991001)86:7<1342::AID-CNCR33>3.0.CO;2-3 |
0.029 |
|
| 1980 |
Sørensen SA, Hasholt L. alpha-Galactosidase isozymes in normal individuals, and in Fabry hemizygotes and heterozygotes. Annals of Human Genetics. 43: 313-21. PMID 6772088 |
0.029 |
|
| 1982 |
Wandall A, Hasholt L, Sørensen SA. Electron microscopic observations on cultured fibroblasts from Fabry heterozygotes and hemizygotes. Ultrastructural Pathology. 3: 51-8. PMID 6280349 |
0.029 |
|
| 1990 |
Sørensen SA. [Ethical aspects in the diagnosis of hereditary diseases, with special reference to Huntington's chorea]. Nordisk Medicin. 105: 2-4. PMID 1967826 |
0.028 |
|
| 1983 |
Sørensen SA, Hasholt L. Attitudes of persons at risk for Fabry's disease towards predictive tests and genetic counselling. Journal of Biosocial Science. 15: 89-94. PMID 6402512 |
0.028 |
|
| 2001 |
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, et al. Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world. European Journal of Human Genetics : Ejhg. 9: 431-6. PMID 11436124 DOI: 10.1038/sj.ejhg.5200656 |
0.028 |
|
| 1993 |
Jensen P, Sørensen SA, Fenger K, Bolwig TG. A study of psychiatric morbidity in patients with Huntington's disease, their relatives, and controls. Admissions to psychiatric hospitals in Denmark from 1969 to 1991. The British Journal of Psychiatry : the Journal of Mental Science. 163: 790-7. PMID 8306121 |
0.027 |
|
| 1989 |
Hasholt L, Wandall A, Sørensen SA. Fabry's disease. Clinical Genetics. 36: 335-6. PMID 2513152 |
0.027 |
|
| 2014 |
Petersen MH, Budtz-Jørgensen E, Sørensen SA, Nielsen JE, Hjermind LE, Vinther-Jensen T, Nielsen SM, Nørremølle A. Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease. Mitochondrion. 17: 14-21. PMID 24836434 DOI: 10.1016/j.mito.2014.05.001 |
0.026 |
|
| 1974 |
Galjaard H, Niermeijer MF, Hahnemann N, Mohr J, Sorensen SA. An example of rapid prenatal diagnosis of Fabry's disease using microtechniques. Clinical Genetics. 5: 368-77. PMID 4211797 |
0.026 |
|
| 1995 |
Madsen KM, Hasholt L, Sørensen SA, Fermér ML, Dahl N. Two novel mutations (L32P) and (G85N) among five different missense mutations in six Danish families with Fabry's disease. Human Mutation. 5: 277-8. PMID 7599642 DOI: 10.1002/humu.1380050316 |
0.026 |
|
| 2000 |
Larsen LA, Svendsen IH, Jensen AM, Kanters JK, Andersen PS, Møller M, Sørensen SA, Sandøe E, Jacobsen JR, Vuust J, Christiansen M. Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2. Clinical Genetics. 57: 125-30. PMID 10735633 DOI: 10.1034/J.1399-0004.2000.570206.X |
0.025 |
|
| 2009 |
Nørremølle A, Budtz-Jørgensen E, Fenger K, Nielsen JE, Sørensen SA, Hasholt L. 4p16.3 haplotype modifying age at onset of Huntington disease. Clinical Genetics. 75: 244-50. PMID 19250382 DOI: 10.1111/j.1399-0004.2008.01136.x |
0.025 |
|
| 2000 |
Hjermind LE, Sørensen SA, Werdelin LM. [Hereditary dystonias]. Ugeskrift For Laeger. 162: 5066-70. PMID 11014135 |
0.025 |
|
| 1974 |
Sorensen SA, Hahnemann N, Mohr J. [Prenatal diagnosis of enzyme defects illustrated by a case of angiokeratoma corporis diffusum (Fabry's disease)]. Ugeskrift For Laeger. 136: 1636-9. PMID 4210817 |
0.023 |
|
| 2000 |
Paixão JA, Silva MR, Sørensen SA, Lebech B, Lander GH, Brown PJ, Langridge S, Talik E, Gonçalves AP. Neutron-scattering study of the magnetic structure ofDyFe4Al8andHoFe4Al8 Physical Review B. 61: 6176-6188. DOI: 10.1103/PHYSREVB.61.6176 |
0.023 |
|
| 2010 |
Sørensen SA. [Residential institutions or long-term units?]. Ugeskrift For Laeger. 172: 731; author reply 73. PMID 20402021 |
0.023 |
|
| 1986 |
Fenger K, Sørensen SA. ADOXI-PLOT: a computer program for plotting pedigrees illustrating autosomal dominant and X-linked inheritance. Computer Methods and Programs in Biomedicine. 23: 47-52. PMID 3638185 |
0.023 |
|
| 1998 |
Løkkegaard T, Nielsen JE, Hasholt L, Fenger K, Werdelin L, Tranebjaerg L, Lauritzen M, Colding-Jørgensen E, Grønbech-Jensen M, Henriksen OA, Sørensen SA. Machado-Joseph disease in three Scandinavian families. Journal of the Neurological Sciences. 156: 152-7. PMID 9588850 |
0.022 |
|
| 2009 |
Saeedi P, Sorensen SA, Hailes S. Performance-aware exploration algorithm for search and rescue robots 2009 Ieee International Workshop On Safety, Security and Rescue Robotics, Ssrr 2009. DOI: 10.1109/SSRR.2009.5424168 |
0.022 |
|
| 1978 |
Sørensen SA, Flodgaard H, Sørensen E. Serum alkaline phosphatase, serum pyrophosphatase, phosphorylethanolamine and inorganic pyrophosphate in plasma and urine. A genetic and clinical study of hypophosphatasia. Monographs in Human Genetics. 10: 66-9. PMID 214699 |
0.022 |
|
| 2001 |
Mellerup E, Bennike B, Bolwig T, Dam H, Hasholt L, Jørgensen MB, Plenge P, Sørensen SA. Platelet serotonin transporters and the transporter gene in control subjects, unipolar patients and bipolar patients. Acta Psychiatrica Scandinavica. 103: 229-33. PMID 11240581 |
0.02 |
|
| 1998 |
Sorensen SA, Low JO. Safety significant class determination of continuous air monitors at facilities handling alpha-emitting radionuclides. Health Physics. 75: 530-4. PMID 9790563 |
0.018 |
|
| 1976 |
Norgaard-Pedersen B, Moller J, Trolle D, Sorensen SA. Alpha-fetoprotein concentration in cord blood from twins and from a set of quadruplets--a case of superfetatio? Human Heredity. 26: 72-80. PMID 60279 |
0.018 |
|
| 2000 |
Sørensen SA. [Preimplantation diagnosis of dominant inherited diseases with late debut]. Ugeskrift For Laeger. 162: 4371-3. PMID 10962958 |
0.017 |
|
| 1998 |
Vigliante A, Christensen MJ, Hill JP, Helgesen G, Sørensen SA, McMorrow DF, Gibbs D, Ward RCC, Wells MR. Interplay between structure and magnetism inHoxPr1−xalloys. II. Resonant x-ray magnetic scattering Physical Review B. 57: 5941-5950. DOI: 10.1103/PHYSREVB.57.5941 |
0.017 |
|
| 1995 |
Mouridsen SE, Sørensen SA. Psychological aspects of von Recklinghausen neurofibromatosis (NF1) Journal of Medical Genetics. 32: 921-4. PMID 8825915 |
0.016 |
|
| 1995 |
Wulff CH, Sørensen SA, Trojaborg W. [X-linked recessive bulbospinal neuropathy (Kennedy syndrome)]. Ugeskrift For Laeger. 157: 6440-1. PMID 7483104 |
0.015 |
|
| 1986 |
Sørensen SA, Mulvihill JJ, Nielsen A. On the natural history of von Recklinghausen neurofibromatosis. Annals of the New York Academy of Sciences. 486: 30-7. PMID 3105394 |
0.014 |
|
| 2010 |
Bono RW, Sorensen SA, Stultz GR. New methodology applying resonant inspection for quality testing of very small powder metal components Advances in Powder Metallurgy and Particulate Materials - 2010, Proceedings of the 2010 International Conference On Powder Metallurgy and Particulate Materials, Powdermet 2010. 1113-1120. |
0.014 |
|
| 2007 |
Mersebach H, Johansson JO, Rasmussen AK, Bengtsson BA, Rosenberg K, Hasholt L, Sørensen SA, Sørensen SS, Feldt-Rasmussen U. Osteopenia: a common aspect of Fabry disease. Predictors of bone mineral density. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 9: 812-8. PMID 18091430 |
0.014 |
|
| 1983 |
Sørensen SA, Jensen OA, Klinken L. Familial aggregation of neuroectodermal and gastrointestinal tumors. Cancer. 52: 1977-80. PMID 6684985 |
0.013 |
|
| 2002 |
Hjermind LE, Werdelin LM, Sørensen SA. Inherited and de novo mutations in sporadic cases of DYT1-dystonia. European Journal of Human Genetics : Ejhg. 10: 213-6. PMID 11973627 DOI: 10.1038/sj.ejhg.5200782 |
0.012 |
|
| 2000 |
Nellemann C, Abell K, Nørremølle A, Løkkegaard T, Naver B, Röpke C, Rygaard J, Sørensen SA, Hasholt L. Inhibition of Huntington synthesis by antisense oligodeoxynucleotides. Molecular and Cellular Neurosciences. 16: 313-23. PMID 11085870 DOI: 10.1006/mcne.2000.0872 |
0.011 |
|
| 2010 |
Saeedi P, Sorensen SA. Multi-agent exploration inside structural collapses Lecture Notes in Electrical Engineering. 60: 373-383. DOI: 10.1007/978-90-481-8776-8_32 |
0.01 |
|
| 2005 |
Luan S, Heintz P, Sorensen S, Jimenez A, Roedersheimer K, Chen D, Wong G. The Effect of Collimator Rotation on IMRT Treatment Planning International Journal of Radiation Oncology*Biology*Physics. 63: S524-S525. DOI: 10.1016/J.Ijrobp.2005.07.886 |
0.01 |
|
| 2000 |
Lund A, Udd B, Juvonen V, Andersen PM, Cederquist K, Ronnevi LO, Sistonen P, Sörensen SA, Tranebjaerg L, Wallgren-Pettersson C, Savontaus ML. Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia. European Journal of Human Genetics : Ejhg. 8: 631-6. PMID 10951525 DOI: 10.1038/sj.ejhg.5200517 |
0.01 |
|
| 1996 |
Van Loo A, Vanholder R, Madsen K, Praet M, Kint J, De Paepe A, Messiaen L, Lameire N, Hasholt L, Sørensen SA, Ringoir S. Novel frameshift mutation in a heterozygous woman with Fabry disease and end-stage renal failure. American Journal of Nephrology. 16: 352-7. PMID 8739292 |
0.01 |
|
| 1988 |
Bachmann Andersen L, Sørensen SA. Diagnosis of von Recklinghausen neurofibromatosis and the Albright syndrome. Two case reports. Neurofibromatosis. 1: 120-3. PMID 3152533 |
0.01 |
|
| 1987 |
Fenger K, Sørensen SA. PEDIGREE-PLOT: a computer program for plotting pedigrees. Clinical Genetics. 32: 284-6. PMID 3677467 |
0.01 |
|
| 1986 |
Larsen M, Krogsaa B, Warburg M, Sørensen SA, Lund-Andersen H. Carriers of X-linked retinitis pigmentosa. A fluorophotometric determination of the permeability of the blood-retinal barrier. Ophthalmic Paediatrics and Genetics. 7: 21-8. PMID 3703487 |
0.01 |
|
| 1986 |
Sørensen SA, Mulvihill JJ, Nielsen A. Long-term follow-up of von Recklinghausen neurofibromatosis. Survival and malignant neoplasms. The New England Journal of Medicine. 314: 1010-5. PMID 3083258 DOI: 10.1056/NEJM198604173141603 |
0.01 |
|
| 1983 |
Hasholt L, Sørensen SA. ConA-mediated binding and uptake of purified alpha-galactosidase A in Fabry fibroblasts. Experimental Cell Research. 148: 405-11. PMID 6313412 |
0.01 |
|
| 1974 |
Hahnemann N, Sorensen SA. Studies on alkaline phosphatase in amniotic fluid. Acta Obstetricia Et Gynecologica Scandinavica. Supplement. 29: 15-21. PMID 4276232 |
0.01 |
|
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