Heiko M Reutter
Overview
Explore the profile of Heiko M Reutter including associated specialties, affiliations and a list of published articles.
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Articles
24
Citations
937
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0
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Recent Articles
1.
Kalanithy J, Mingardo E, Stegmann J, Dhakar R, Dakal T, Rosenfeld J, et al.
J Med Genet
. 2024 Dec;
62(2):126-137.
PMID: 39715634
Background: Previous studies in mouse, and zebrafish embryos show strong expression in progenitor cells of neuronal and neural crest tissues suggesting its involvement in neural crest specification. However, the role...
2.
Whitchurch J, Schneider S, Hilger A, Kollges R, Stegmann J, Waffenschmidt L, et al.
Cells
. 2024 Jan;
13(2).
PMID: 38247840
Besides visceral heterotaxia, null mouse embryos exhibit general edema and perinatal lethality. In humans, congenital chylothorax (CCT) is a frequent cause of fetal hydrops. In 2021, Correa and colleagues reported...
3.
Kolvenbach C, Felger T, Schierbaum L, Thiffault I, Pastinen T, Szczepanska M, et al.
J Med Genet
. 2022 Nov;
60(6):587-596.
PMID: 36379543
Background: is thought to play an important role in cytoskeletal modification and development of the early nervous system. Previously, single-nucleotide variants (SNVs) or copy number variations (CNVs) in have been...
4.
5.
Dworschak G, van Rooij I, Reutter H
Genes (Basel)
. 2021 Sep;
12(9).
PMID: 34573284
Anorectal malformations (ARM) represent a rare birth defect of the hindgut that occur in approximately 1 in 3000 live births. Around 60% of ARM occur with associated anomalies including defined...
6.
Ebach F, Hainmann I, Eis-Hubinger A, Escherisch G, Dilloo D, Reutter H, et al.
Pediatr Blood Cancer
. 2021 May;
68(9):e29100.
PMID: 34022118
No abstract available.
7.
Dworschak G, Reutter H, Ludwig M
Orphanet J Rare Dis
. 2021 Apr;
16(1):167.
PMID: 33836786
Background: The triad of a presacral mass, sacral agenesis and an anorectal anomaly constitutes the rare Currarino syndrome (CS), which is caused by dorsal-ventral patterning defects during embryonic development. The...
8.
Connaughton D, Dai R, Owen D, Marquez J, Mann N, Graham-Paquin A, et al.
Am J Hum Genet
. 2020 Sep;
107(4):727-742.
PMID: 32891193
Congenital anomalies of the kidney and urinary tract (CAKUT) constitute one of the most frequent birth defects and represent the most common cause of chronic kidney disease in the first...
9.
van de Putte R, Dworschak G, Brosens E, Reutter H, Marcelis C, Acuna-Hidalgo R, et al.
Front Pediatr
. 2020 Jul;
8:310.
PMID: 32656166
The VATER/VACTERL association (VACTERL) is defined as the non-random occurrence of the following congenital anomalies: Vertebral, Anal, Cardiac, Tracheal-Esophageal, Renal, and Limb anomalies. As no unequivocal candidate gene has been...
10.
Ebert A, Zwink N, Reutter H, Jenetzky E, Stein R, Holscher A, et al.
Front Pediatr
. 2020 Jun;
8:174.
PMID: 32509709
To evaluate the impact of reconstructive strategies and post-operative management on short- and long-term surgical outcome and complications of classical bladder exstrophy (CBE) patients' comprehensive data of the multicenter German-wide...