Andreas D Zimmer
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Explore the profile of Andreas D Zimmer including associated specialties, affiliations and a list of published articles.
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29
Citations
1816
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Recent Articles
1.
Hotz A, Kopp J, Bourrat E, Oji V, Sussmuth K, Komlosi K, et al.
Genes (Basel)
. 2023 Mar;
14(3).
PMID: 36980989
Autosomal recessive congenital ichthyosis (ARCI) is a non-syndromic congenital disorder of cornification characterized by abnormal scaling of the skin. The three major phenotypes are lamellar ichthyosis, congenital ichthyosiform erythroderma, and...
2.
Jagle S, Hsu H, Juratli H, Zimmer A, Prieschl A, Alter S, et al.
Br J Dermatol
. 2023 Jan;
188(1):94-99.
PMID: 36689507
Background: Hyperkeratosis lenticularis perstans (HLP), also known as Flegel disease, is a rare skin disease presenting with asymptomatic small hyperkeratotic papules. The lesions often appear on the dorsal feet and...
3.
Ennouri M, Zimmer A, Bahloul E, Chaabouni R, Marrakchi S, Turki H, et al.
BMC Med Genomics
. 2022 Jan;
15(1):4.
PMID: 34983512
Background: Ichthyosis is a heterogeneous group of Mendelian cornification disorders that includes syndromic and non-syndromic forms. Autosomal Recessive Congenital Ichthyosis (ARCI) and Ichthyosis Linearis Circumflexa (ILC) belong to non-syndromic forms....
4.
Komlosi K, Claris O, Collardeau-Frachon S, Kopp J, Hausser I, Mazereeuw-Hautier J, et al.
Front Genet
. 2021 Dec;
12:719624.
PMID: 34956305
Neonatal collodion baby or ichthyosis can pose a diagnostic challenge, and in many cases, only additional organ involvement or the course of the disease will help differentiate between non-syndromic and...
5.
Resch L, Hotz A, Zimmer A, Komlosi K, Singh N, Tzschach A, et al.
Genes (Basel)
. 2021 Oct;
12(10).
PMID: 34680878
In about 20-30% of all women with breast cancer, an increased number of cases of breast cancer can be observed in their family history. However, currently, only 5-10% of all...
6.
Hotz A, Kopp J, Bourrat E, Oji V, Komlosi K, Giehl K, et al.
Genes (Basel)
. 2021 Jan;
12(1).
PMID: 33435499
The autosomal recessive congenital ichthyoses (ARCI) are a nonsyndromic group of cornification disorders that includes lamellar ichthyosis, congenital ichthyosiform erythroderma, and harlequin ichthyosis. To date mutations in ten genes have...
7.
Komlosi K, Glaser S, Kopp J, Hotz A, Alter S, Zimmer A, et al.
JIMD Rep
. 2020 Sep;
55(1):51-58.
PMID: 32905044
Many of the genetic childhood disorders leading to death in the perinatal period follow autosomal recessive inheritance and bear specific challenges for genetic counseling and prenatal diagnostics. Often, affected children...
8.
Ballin N, Hotz A, Bourrat E, Kusel J, Oji V, Bouadjar B, et al.
Hum Mutat
. 2019 Jul;
40(12):2318-2333.
PMID: 31347739
Autosomal recessive congenital ichthyosis (ARCI) belongs to a heterogeneous group of disorders of keratinization. To date, 10 genes have been identified to be causative for ARCI. NIPAL4 (Nipa-Like Domain-Containing 4)...
9.
Horer S, Marrakchi S, Radner F, Zolles G, Heinz L, Eichmann T, et al.
J Invest Dermatol
. 2019 May;
139(10):2154-2163.e5.
PMID: 31082376
Trichilemmal cysts are common hair follicle-derived intradermal cysts. The trait shows an autosomal dominant mode of transmission with incomplete penetrance. Here, we describe the pathogenetic mechanism for the development of...
10.
Rauschendorf M, Zimmer A, Laut A, Demmer P, Rosler B, Happle R, et al.
Pigment Cell Melanoma Res
. 2018 Aug;
32(1):85-91.
PMID: 30117279
No abstract available.