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Search life-sciences literature (45,104,145 articles, preprints and more)

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External validation of the computer aided risk scoring system in predicting in-hospital mortality following emergency medical admissions.
Kingsley V, Fox L, Simm D, Martin GP, Thompson W, Faisal M
Int J Med Inform, 188:105497, 18 May 2024
Cited by: 0 articles | PMID: 38781886
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Design of typical genes for heterologous gene expression.
Simm D, Popova B, Braus GH, Waack S, Kollmar M
Sci Rep, 12(1):9625, 10 Jun 2022
Cited by: 1 article | PMID: 35688911 | PMCID: PMC9187722
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Critical assessment of coiled-coil predictions based on protein structure data.
Simm D, Hatje K, Waack S, Kollmar M
Sci Rep, 11(1):12439, 14 Jun 2021
Cited by: 6 articles | PMID: 34127723 | PMCID: PMC8203680
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The Protein-Coding Human Genome: Annotating High-Hanging Fruits.
Hatje K, Mühlhausen S, Simm D, Kollmar M
Bioessays, 41(11):e1900066, 23 Sep 2019
Cited by: 10 articles | PMID: 31544971
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Protein function prediction in genomes: Critical assessment of coiled-coil predictions based on protein structure data
Simm D, Hatje K, Waack S, Kollmar M
bioRxiv, 18 Jun 2019
Cited by: 1 article | PPR: PPR82864
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Waggawagga-CLI: A command-line tool for predicting stable single α-helices (SAH-domains), and the SAH-domain distribution across eukaryotes.
Simm D, Kollmar M
PLoS One, 13(2):e0191924, 14 Feb 2018
Cited by: 5 articles | PMID: 29444145 | PMCID: PMC5812594
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The landscape of human mutually exclusive splicing.
Hatje K, Rahman RU, Vidal RO, Simm D, Hammesfahr B, Bansal V, Rajput A, Mickael ME, Sun T, Bonn S, Kollmar M
Mol Syst Biol, 13(12):959, 14 Dec 2017
Cited by: 36 articles | PMID: 29242366 | PMCID: PMC5740500
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Identifying Sequenced Eukaryotic Genomes and Transcriptomes with diArk.
Kollmar M, Simm D
Methods Mol Biol, 1757:1-19, 01 Jan 2018
Cited by: 0 articles | PMID: 29761453
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Correction: Distribution and evolution of stable single α-helices (SAH domains) in myosin motor proteins.
Simm D, Hatje K, Kollmar M
PLoS One, 12(5):e0177716, 11 May 2017
Cited by: 0 articles | PMID: 28493992 | PMCID: PMC5426705
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Distribution and evolution of stable single α-helices (SAH domains) in myosin motor proteins.
Simm D, Hatje K, Kollmar M
PLoS One, 12(4):e0174639, 03 Apr 2017
Cited by: 8 articles | PMID: 28369123 | PMCID: PMC5378345
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The landscape of human mutually exclusive splicing
Hatje K, Vidal RO, Rahman R, Simm D, Hammesfahr B, Shomroni O, Bonn S, Kollmar M
bioRxiv, 02 May 2017
Cited by: 0 articles | PPR: PPR20564
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diArk--the database for eukaryotic genome and transcriptome assemblies in 2014.
Kollmar M, Kollmar L, Hammesfahr B, Simm D
Nucleic Acids Res, 43(database issue):D1107-12, 06 Nov 2014
Cited by: 3 articles | PMID: 25378341 | PMCID: PMC4384042
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Waggawagga: comparative visualization of coiled-coil predictions and detection of stable single α-helices (SAH domains).
Simm D, Hatje K, Kollmar M
Bioinformatics, 31(5):767-769, 22 Oct 2014
Cited by: 42 articles | PMID: 25338722
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Adiponectin levels are high in children with classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency.
Völkl TM, Simm D, Körner A, Kiess W, Kratzsch J, Dörr HG
Acta Paediatr, 98(5):885-891, 19 Feb 2009
Cited by: 9 articles | PMID: 19236311
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Two novel mutations in the human thyroid peroxidase (TPO) gene: genetics and clinical findings in four children.
Simm D, Pfarr N, Pohlenz J, Prawitt D, Dörr HG
Acta Paediatr, 98(6):1057-1061, 20 Feb 2009
Cited by: 3 articles | PMID: 19243353
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Does an altered leptin axis play a role in obesity among children and adolescents with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency?
Völkl TM, Simm D, Körner A, Rascher W, Kiess W, Kratzsch J, Dörr HG
Eur J Endocrinol, 160(2):239-247, 12 Nov 2008
Cited by: 18 articles | PMID: 19004982
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[Chronological age of patients with Turner syndrome at diagnosis].
Simm D, Degenhardt K, Gerdemann C, Völkl TM, Rauch A, Dörr HG
Klin Padiatr, 220(1):16-20, 20 Dec 2007
Cited by: 2 articles | PMID: 18095252
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Altered 24-hour blood pressure profiles in children and adolescents with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Völkl TM, Simm D, Dötsch J, Rascher W, Dörr HG
J Clin Endocrinol Metab, 91(12):4888-4895, 26 Sep 2006
Cited by: 45 articles | PMID: 17003094
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Catch-down growth during infancy of children born small (SGA) or appropriate (AGA) for gestational age with short-statured parents.
Völkl TM, Haas B, Beier C, Simm D, Dörr HG
J Pediatr, 148(6):747-752, 01 Jun 2006
Cited by: 6 articles | PMID: 16769380
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Obesity among children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Völkl TM, Simm D, Beier C, Dörr HG
Pediatrics, 117(1):e98-105, 01 Jan 2006
Cited by: 78 articles | PMID: 16396852
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Spontaneous growth hormone secretion and IGF1:IGFBP3 molar ratios in children born small for gestational age (SGA).
Völkl TM, Schwöbel K, Simm D, Beier C, Rohrer TR, Dörr HG
Growth Horm IGF Res, 14(6):455-461, 01 Dec 2004
Cited by: 5 articles | PMID: 15519254
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Cardiovascular anomalies in children and young adults with Ullrich-Turner syndrome the Erlangen experience.
Völkl TM, Degenhardt K, Koch A, Simm D, Dörr HG, Singer H
Clin Cardiol, 28(2):88-92, 01 Feb 2005
Cited by: 37 articles | PMID: 15757080 | PMCID: PMC6654047
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