Cornelia Daumer‐Haas

1.1k citations

10 papers · 451 indexed · h-index 8

Impact in

Genetics top 10%
- Craniofacial Disorders and Treatments
- Genomic variations and chromosomal abnormalities
- Cleft Lip and Palate Research
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics

Papers in ⓘ

Genetics 8
- Genomic variations and chromosomal abnormalities 5
- Cleft Lip and Palate Research 2
- Craniofacial Disorders and Treatments 2
- Ocular Disorders and Treatments 2
Pediatrics, Perinatology and Child Health 4
- Prenatal Screening and Diagnostics 4

Co-authors: Ute Hehr (2 shared papers)Jill Dixon (1 shared paper)Simone Schuffenhauer (4 shared papers)Dietmar Lohmann (1 shared paper)A. Jeannette M. Hoogeboom (1 shared paper)Christiane Zweier (1 shared paper)Arie van Haeringen (1 shared paper)Claudia Ruivenkamp (1 shared paper)
Journals: Communications Biology (2 papers)Nature Genetics (1 paper)The American Journal of Human Genetics (1 paper)Human Genetics (1 paper)Gene (1 paper)
Partner nations: Germany United States Israel

In The Last Decade

Cornelia Daumer‐Haas

10 papers receiving 440 citations

Peers

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-authors

The 25 scholars most cited alongside Cornelia Daumer‐Haas, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Cornelia Daumer‐Haas Line = papers co-authored together Cornelia Daumer‐Haas links everyone, so they are left out of the graph.

All Works

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10 of 10 papers shown

#	Work
1	Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome Nature Genetics ·Johannes G. Dauwerse, Jill Dixon, Saskia Seland, Claudia Ruivenkamp, Arie van Haeringen, Lies H. Hoefsloot, Dorien J.M. Peters, Agnes Clement-de Boers, Cornelia Daumer‐Haas, Robert Maiwald, Christiane Zweier, Bronwyn Kerr, Ana María Cobo, Joaquín Fernández Toral, A. Jeannette M. Hoogeboom, Dietmar Lohmann, Ute Hehr, Michael J. Dixon, Martijn H. Breuning, Dagmar Wieczorek	2010	243
2	Multiplex-FISH for Pre- and Postnatal Diagnostic Applications The American Journal of Human Genetics ·Sabine Uhrig, Simone Schuffenhauer, Christine Fauth, Antje Wirtz, Cornelia Daumer‐Haas, Can Apacik, Monika Cohen, Jutta Müller‐Navia, Thomas Cremer, Jan Murken, Michael R. Speicher	1999	72
3	Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation Communications Biology ·Alexandra Stavsky, Ohad Stoler, Marko Kostić, Tomer Katoshevsky, Essam A. Assali, Ivana Savic, Yael Amitai, Holger Prokisch, Steffen Leiz, Cornelia Daumer‐Haas, Ilya A. Fleidervish, Fabiana Perocchi, Daniel Gitler, Israel Sekler	2021	33
4	Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly Human Genetics ·Ute Hehr, Daniel Pineda‐Alvarez, Goekhan Uyanik, Ping Hu, Nan Zhou, Andreas Hehr, Chayim Schell-Apacik, Carola Altus, Cornelia Daumer‐Haas, A Meiner, Peter Steuernagel, Erich Roessler, Jürgen Winkler, Maximilian Muenke	2010	33
5	Tetrasomy 21 pter→q22.1 and Down syndrome: Molecular definition of the region American Journal of Medical Genetics ·Cornelia Daumer‐Haas, Simone Schuffenhauer, Joachim U. Walther, Roberton D. Schipper, T Porstmann, Julie R. Korenberg	1994	19
6	Expanding the mutation spectrum for Fraser syndrome: Identification of a novel heterozygous deletion in FRAS1 Gene ·Julia Hoefele, Christian Wilhelm, Monika Schiesser, Reinhold Mack, Uwe Heinrich, Lutz T. Weber, Saskia Biskup, Cornelia Daumer‐Haas, Hanns‐Georg Klein, Imma Rost	2013	17
7	Delineation of a 2q deletion in a girl with dysmorphic features and epilepsy American Journal of Medical Genetics Part A ·Sabine Langer, Jochen B. Geigl, Janine Wagenstaller, Gaby Lederer, Maja Hempel, Cornelia Daumer‐Haas, H.-J. Leifheit, Michael R. Speicher	2006	16
8	Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cen American Journal of Medical Genetics ·Simone Schuffenhauer, Albrecht Kobelt, Cornelia Daumer‐Haas, Christine Löffler, Gisela Müller, Jan Murken, Thomas Meitinger	1996	13
9	Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13‐cen American Journal of Medical Genetics ·Simone Schuffenhauer, Albrecht Kobelt, Cornelia Daumer‐Haas, Christine Löffler, Gisela Müller, Jan Murken, Thomas Meitinger	1996	3
10	Author Correction: Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation Communications Biology ·Alexandra Stavsky, Ohad Stoler, Marko Kostić, Tomer Katoshevsky, Essam A. Assali, Ivana Savic, Yael Amitai, Holger Prokisch, Steffen Leiz, Cornelia Daumer‐Haas, Ilya A. Fleidervish, Fabiana Perocchi, Daniel Gitler, Israel Sekler	2021	2

About Cornelia Daumer‐Haas

Cornelia Daumer‐Haas is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Genetics, Plant Science and Pathology and Forensic Medicine, having authored 10 papers that have together received 451 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers), Chromosomal and Genetic Variations (3 papers), Cleft Lip and Palate Research (2 papers), Craniofacial Disorders and Treatments (2 papers), Ocular Disorders and Treatments (2 papers), Ion channel regulation and function (1 paper) and Reconstructive Facial Surgery Techniques (1 paper). The work is most often cited by research in Genetics (264 citations), Pediatrics, Perinatology and Child Health (73 citations), Molecular Biology (245 citations), Genetics (36 citations) and Developmental Biology (6 citations). Cornelia Daumer‐Haas has collaborated with scholars based in Germany, United States and Israel. Frequent co-authors include Ute Hehr, Jill Dixon, Simone Schuffenhauer, Dietmar Lohmann, A. Jeannette M. Hoogeboom, Christiane Zweier, Arie van Haeringen, Claudia Ruivenkamp, Martijn H. Breuning and Lies H. Hoefsloot. Their work appears in journals such as Communications Biology, Nature Genetics, The American Journal of Human Genetics, Human Genetics and Gene.

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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