Cornelia Daumer‐Haas

1.1k total citations
10 papers, 451 citations indexed

About

Cornelia Daumer‐Haas is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Cornelia Daumer‐Haas has authored 10 papers receiving a total of 451 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in Cornelia Daumer‐Haas's work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). Cornelia Daumer‐Haas is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). Cornelia Daumer‐Haas collaborates with scholars based in Germany, United States and Israel. Cornelia Daumer‐Haas's co-authors include Ute Hehr, Jill Dixon, Saskia Seland, Simone Schuffenhauer, Lies H. Hoefsloot, Dorien J.M. Peters, A. Jeannette M. Hoogeboom, Robert Maiwald, Christiane Zweier and Arie van Haeringen and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Gene.

In The Last Decade

Cornelia Daumer‐Haas

10 papers receiving 440 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Cornelia Daumer‐Haas Germany 8 264 245 73 62 48 10 451
Patricia Heard United States 13 391 1.5× 210 0.9× 111 1.5× 98 1.6× 30 0.6× 22 499
Kelly E. Jackson United States 8 211 0.8× 204 0.8× 50 0.7× 40 0.6× 20 0.4× 15 375
Nathalie Marle France 11 237 0.9× 170 0.7× 56 0.8× 42 0.7× 29 0.6× 23 373
Bridgette Soileau United States 11 345 1.3× 165 0.7× 102 1.4× 71 1.1× 27 0.6× 16 408
Janice C. Palumbos United States 8 161 0.6× 245 1.0× 56 0.8× 28 0.5× 82 1.7× 13 391
Ho‐Ming Luk China 13 267 1.0× 249 1.0× 100 1.4× 19 0.3× 50 1.0× 67 471
Jim Mullikin United States 10 195 0.7× 245 1.0× 68 0.9× 96 1.5× 27 0.6× 14 379
Patricia D. Ghidoni United States 7 257 1.0× 181 0.7× 99 1.4× 71 1.1× 21 0.4× 8 329
Lorraine Gaunt United Kingdom 10 249 0.9× 146 0.6× 108 1.5× 50 0.8× 17 0.4× 16 368
Elisabeth A. Keitges United States 11 439 1.7× 249 1.0× 85 1.2× 105 1.7× 16 0.3× 13 529

Countries citing papers authored by Cornelia Daumer‐Haas

Since Specialization
Citations

This map shows the geographic impact of Cornelia Daumer‐Haas'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 Cornelia Daumer‐Haas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cornelia Daumer‐Haas more than expected).

Fields of papers citing papers by Cornelia Daumer‐Haas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cornelia Daumer‐Haas. 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 Cornelia Daumer‐Haas. The network helps show where Cornelia Daumer‐Haas may publish in the future.

Co-authorship network of co-authors of Cornelia Daumer‐Haas

This figure shows the co-authorship network connecting the top 25 collaborators of Cornelia Daumer‐Haas. A scholar is included among the top collaborators of Cornelia Daumer‐Haas 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 Cornelia Daumer‐Haas. Cornelia Daumer‐Haas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Kostić, Marko, Essam A. Assali, Yael Amitai, et al.. (2021). Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation. Communications Biology. 4(1). 666–666. 33 indexed citations
2.
Kostić, Marko, Essam A. Assali, Yael Amitai, et al.. (2021). Author Correction: Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation. Communications Biology. 4(1). 755–755. 2 indexed citations
3.
Hoefele, Julia, Christian Wilhelm, Monika Schiesser, et al.. (2013). Expanding the mutation spectrum for Fraser syndrome: Identification of a novel heterozygous deletion in FRAS1. Gene. 520(2). 194–197. 17 indexed citations
4.
Dauwerse, Johannes G., Jill Dixon, Saskia Seland, et al.. (2010). Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome. Nature Genetics. 43(1). 20–22. 243 indexed citations
5.
Hehr, Ute, Daniel Pineda‐Alvarez, Goekhan Uyanik, et al.. (2010). Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly. Human Genetics. 127(5). 555–561. 33 indexed citations
6.
Langer, Sabine, Jochen B. Geigl, Janine Wagenstaller, et al.. (2006). Delineation of a 2q deletion in a girl with dysmorphic features and epilepsy. American Journal of Medical Genetics Part A. 140A(7). 764–768. 16 indexed citations
7.
Uhrig, Sabine, Simone Schuffenhauer, Christine Fauth, et al.. (1999). Multiplex-FISH for Pre- and Postnatal Diagnostic Applications. The American Journal of Human Genetics. 65(2). 448–462. 72 indexed citations
8.
Schuffenhauer, Simone, et al.. (1996). Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cen. American Journal of Medical Genetics. 65(1). 56–59. 13 indexed citations
9.
Schuffenhauer, Simone, et al.. (1996). Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13‐cen. American Journal of Medical Genetics. 65(1). 56–59. 3 indexed citations
10.
Daumer‐Haas, Cornelia, et al.. (1994). Tetrasomy 21 pter→q22.1 and Down syndrome: Molecular definition of the region. American Journal of Medical Genetics. 53(4). 359–365. 19 indexed citations

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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