C Rosenberg
Overview
Explore the profile of C Rosenberg including associated specialties, affiliations and a list of published articles.
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Articles
229
Citations
4182
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Recent Articles
1.
Carvalho L, da Costa S, Campagnari F, Kaufman A, Bertola D, da Silva I, et al.
J Intellect Disabil Res
. 2021 Oct;
65(12):1049-1057.
PMID: 34713510
Background: Genetic variants involving the MED13L gene can lead to an autosomal dominant syndrome characterised by intellectual disability/developmental delay and facial dysmorphism. Methods: We investigated two cases (one familial and...
2.
Griesi-Oliveira K, Fogo M, Pinto B, Alves A, Suzuki A, Morales A, et al.
Mol Psychiatry
. 2020 Feb;
26(5):1589-1605.
PMID: 32060413
Evaluation of expression profile in autism spectrum disorder (ASD) patients is an important approach to understand possible similar functional consequences that may underlie disease pathophysiology regardless of its genetic heterogeneity....
3.
Krepischi A, Maschietto M, Ferreira E, Silva A, Costa S, da Cunha I, et al.
Mol Cytogenet
. 2016 Feb;
9:20.
PMID: 26913079
Background: Wilms tumor (WT) has a not completely elucidated pathogenesis. DNA copy number alterations (CNAs) are common in cancer, and often define key pathogenic events. The aim of this work...
4.
Rosenberg C, Freitas E, Uehara D, Auricchio M, Costa S, Oiticica J, et al.
Clin Genet
. 2015 Oct;
89(4):473-477.
PMID: 26456090
Genetic heterogeneity has made the identification of genes related to hearing impairment a challenge. In the absence of a clear phenotypic aetiology, recurrence risk estimates are often based on family...
5.
Lewin A, Rosenberg C, H Meyer Z, Wong C, Nelson L, Manen J, et al.
Plant Mol Biol
. 2013 Dec;
8(6):447-59.
PMID: 24301307
Specificity in legume-Rhizobium symbiosis depends on plant and rhizobial genes. As our objective was to study broad host-range determinants of rhizobia, we sought a legume and a Rhizobium with the...
6.
Dornelles-Wawruk H, Pic-Taylor A, Rosenberg C, Krepischi A, Safatle H, Ferrari I, et al.
Mol Syndromol
. 2013 Oct;
4(6):297-301.
PMID: 24167466
We report on a patient carrying a 17q21.31 microdeletion and exhibiting many common syndrome features, together with other clinical signs which have rarely or never been described to date. The...
7.
Hegenscheid K, Puls R, Rosenberg C
Radiologe
. 2012 Nov;
52(11):980-6.
PMID: 23154845
Injuries of the knees are common. The Ottawa knee rule provides decisional support to determine whether radiographs are indicated or not. With the use of ultrasound it is possible to...
8.
Rosenberg C, Hoffmann C, Mensel B, Puls R, Hosten N
Radiologe
. 2012 Jan;
52(1):15-21.
PMID: 22249697
Laser ablation (LA) is momentarily the only invasive ablation procedure besides radiofrequency ablation (RFA) which can be performed entirely under magnetic resonance imaging (MRI) guidance. The long-term outcome and morbidity...
9.
Puls R, Rosenberg C, Kuhn J, Traeger T, Mensel B, Hoene A
Rofo
. 2011 Dec;
184(1):15-23.
PMID: 22198828
The treatment of thoracic aortic diseases has undergone a paradigm shift due to the introduction and further development of interventional techniques in recent years. Thoracic endovascular aortic repair (TEVAR) of...
10.
Molin A, Andrieux J, Koolen D, Malan V, Carella M, Colleaux L, et al.
J Med Genet
. 2011 Dec;
49(2):104-9.
PMID: 22180640
Background: Congenital deletions affecting 3q11q23 have rarely been reported and only five cases have been molecularly characterised. Genotype-phenotype correlation has been hampered by the variable sizes and breakpoints of the...