Dagmar Wahl

403 total citations
6 papers, 189 citations indexed

About

Dagmar Wahl is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Dagmar Wahl has authored 6 papers receiving a total of 189 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Genetics. Recurrent topics in Dagmar Wahl's work include Hedgehog Signaling Pathway Studies (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Congenital limb and hand anomalies (1 paper). Dagmar Wahl is often cited by papers focused on Hedgehog Signaling Pathway Studies (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Congenital limb and hand anomalies (1 paper). Dagmar Wahl collaborates with scholars based in Germany, United States and Poland. Dagmar Wahl's co-authors include Bettina Lorenz‐Depiereux, Janine Wagenstaller, Stephanie Spranger, Michaela Nathrath, Babett Heye, Thomas Meitinger, Volkmar Liebscher, Bernd Kazmierczak, Tim M. Strom and Dieter Gläser and has published in prestigious journals such as The American Journal of Human Genetics, Clinical Genetics and European Journal of Pediatrics.

In The Last Decade

Dagmar Wahl

6 papers receiving 184 citations

Peers

Countries citing papers authored by Dagmar Wahl

Since Specialization

Citations

This map shows the geographic impact of Dagmar Wahl's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Dagmar Wahl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dagmar Wahl more than expected).

Fields of papers citing papers by Dagmar Wahl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dagmar Wahl. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Dagmar Wahl. The network helps show where Dagmar Wahl may publish in the future.

Co-authorship network of co-authors of Dagmar Wahl

This figure shows the co-authorship network connecting the top 25 collaborators of Dagmar Wahl. A scholar is included among the top collaborators of Dagmar Wahl based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Dagmar Wahl. Dagmar Wahl is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	Overgrowth-associated partial trisomy 15q24.3-qter and mosaic 11p15.5 duplication involving Silver-Russell region in a patient with lateralized asymmetry and developmental delay 2021 ·Clinical Dysmorphology ·(unknown), Michael C. Frühwald, Uwe Heinrich, (unknown), Dagmar Wahl, Thomas Eggermann	1
2	Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis 2018 ·Frontiers in Pediatrics ·Matthias C. Braunisch, Maike Büttner‐Herold, Roman Günthner, Robin Satanovskij, Korbinian M. Riedhammer, (unknown), Hanns‐Georg Klein, Dagmar Wahl, Claudius Küchle, Lutz Renders, Uwe Heemann, Christoph Schmaderer, Julia Hoefele	13
3	Copy-Number Variations Measured by Single-Nucleotide–Polymorphism Oligonucleotide Arrays in Patients with Mental Retardation 2007 ·The American Journal of Human Genetics ·Janine Wagenstaller, Stephanie Spranger, Bettina Lorenz‐Depiereux, Bernd Kazmierczak, Michaela Nathrath, Dagmar Wahl, Babett Heye, Dieter Gläser, Volkmar Liebscher, Thomas Meitinger, Tim M. Strom	93
4	Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the sonic hedgehog gene and the HLXB9 gene at 7q36.3 2004 ·American Journal of Medical Genetics Part A ·Denise Horn, Holger Tönnies, Heidemarie Neitzel, Dagmar Wahl, Georg Klaus Hinkel, Arpad von Moers, Oliver Bartsch	37
5	Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation 2004 ·European Journal of Pediatrics ·Ute Hehr, Claudia Groß, (unknown), Dagmar Wahl, (unknown), Peter H. Heidemann, Andreas Hehr, (unknown)	40
6	Spinal and bulbar muscular atrophy (SBMA): Somatic stability of an expanded CAG repeat in fetal tissues 1998 ·Clinical Genetics ·Kerry Baldwin Jedele, Dagmar Wahl, (unknown), Antje Wirtz, Jan Murken, Elke Holinski‐Feder	5

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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