Maria Kirchhoff
About
Maria Kirchhoff is a scholar working on Genetics, Molecular Biology and Plant Science.
According to data from OpenAlex, Maria Kirchhoff has authored 65 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 25 papers in Molecular Biology and 14 papers in Plant Science. Recurrent topics in Maria Kirchhoff's work include Genomic variations and chromosomal abnormalities (40 papers), Chromosomal and Genetic Variations (14 papers) and Congenital heart defects research (12 papers). Maria Kirchhoff is often cited by papers focused on Genomic variations and chromosomal abnormalities (40 papers), Chromosomal and Genetic Variations (14 papers) and Congenital heart defects research (12 papers). Maria Kirchhoff collaborates with scholars based in Denmark, Germany and United States. Maria Kirchhoff's co-authors include Tommy Gerdes, Claes Lundsteen, Hanne Rose, Jan Maahr, Anne‐Marie Bisgaard, Thue Bryndorf, Jens Kastrup, Roberto S Oliveri, Krzysztof T. Drzewiecki and Peter V. Glovinski and has published in prestigious journals such as The Lancet, Experimental Cell Research and Journal of Medical Genetics.
In The Last Decade
Maria Kirchhoff
65 papers receiving 2.4k citations
Hit Papers
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late) cites · hero ref
| Name | h | Career | Trend | Papers | Cites | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| Maria Kirchhoff Denmark | 26 | 1.3k | 909 | 615 | 575 | 410 | 65 | 2.5k | ||
| Gérard Tachdjian France | 28 | 973 0.8× | 1.5k 1.7× | 483 0.8× | 780 1.4× | 893 2.2× | 113 | 3.4k | ||
| Stephen Abbs United Kingdom | 37 | 1.0k 0.8× | 3.0k 3.3× | 853 1.4× | 347 0.6× | 359 0.9× | 83 | 4.0k | ||
| Gopalrao V.N. Velagaleti United States | 17 | 507 0.4× | 594 0.7× | 512 0.8× | 355 0.6× | 152 0.4× | 74 | 1.5k | ||
| Francesca Novara Italy | 24 | 579 0.4× | 881 1.0× | 895 1.5× | 505 0.9× | 127 0.3× | 56 | 2.3k | ||
| B S Emanuel United States | 30 | 1.1k 0.8× | 1.8k 2.0× | 459 0.7× | 243 0.4× | 257 0.6× | 44 | 2.9k | ||
| Ben Van Handel United States | 26 | 283 0.2× | 2.1k 2.3× | 689 1.1× | 446 0.8× | 247 0.6× | 39 | 2.9k | ||
| Jürgen Kohlhase Germany | 33 | 1.0k 0.8× | 1.7k 1.9× | 235 0.4× | 287 0.5× | 195 0.5× | 91 | 2.7k | ||
| Joyce Axelman United States | 21 | 980 0.8× | 1.9k 2.1× | 246 0.4× | 365 0.6× | 147 0.4× | 32 | 2.6k | ||
| Lygia V. Pereira Brazil | 28 | 2.3k 1.7× | 1.5k 1.7× | 436 0.7× | 443 0.8× | 117 0.3× | 94 | 4.0k | ||
| Muriel Holder‐Espinasse France | 26 | 1.0k 0.8× | 1.1k 1.2× | 169 0.3× | 358 0.6× | 176 0.4× | 74 | 2.0k |
Countries citing papers authored by Maria Kirchhoff
Since
Specialization
Citations
This map shows the geographic impact of Maria Kirchhoff'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 Maria Kirchhoff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maria Kirchhoff more than expected).
Fields of papers citing papers by Maria Kirchhoff
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Maria Kirchhoff. 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 Maria Kirchhoff. The network helps show where Maria Kirchhoff may publish in the future.
Co-authorship network of co-authors of Maria Kirchhoff
This figure shows the co-authorship network connecting the top 25 collaborators of Maria Kirchhoff. A scholar is included among the top collaborators of Maria Kirchhoff 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 Maria Kirchhoff. Maria Kirchhoff is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Singh, Ram J., Ana S.A. Cohen, Geetu Mendiratta, et al.. (2021). Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay. Molecular Case Studies. 7(3). a005991–a005991.
2.
Juhl, Morten, Josefine Tratwal, Bjarke Follin, et al.. (2016). Comparison of clinical grade human platelet lysates for cultivation of mesenchymal stromal cells from bone marrow and adipose tissue. Scandinavian Journal of Clinical and Laboratory Investigation. 76(2). 93–104.
3.
Kølle, Stig-Frederik Trojahn, Roberto S Oliveri, Peter V. Glovinski, et al.. (2013). Pooled human platelet lysate versus fetal bovine serum—investigating the proliferation rate, chromosome stability and angiogenic potential of human adipose tissue-derived stem cells intended for clinical use. Cytotherapy. 15(9). 1086–1097.
4.
Kølle, Stig-Frederik Trojahn, Anne Fischer‐Nielsen, Anders Bruun Mathiasen, et al.. (2013). Enrichment of autologous fat grafts with ex-vivo expanded adipose tissue-derived stem cells for graft survival: a randomised placebo-controlled trial. The Lancet. 382(9898). 1113–1120.
5.
Schejbel, Lone, Ida Maria Schmidt, Maria Kirchhoff, et al.. (2011). Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation. Genes and Immunity. 12(2). 90–99.
6.
Stockhausen, Marie‐Thérése, Helle Broholm, Mette Villingshøj, et al.. (2011). Maintenance of EGFR and EGFRvIII expressions in an in vivo and in vitro model of human glioblastoma multiforme. Experimental Cell Research. 317(11). 1513–1526.
7.
Wohlleber, Eva, Maria Kirchhoff, Alexander M. Zink, et al.. (2010). Clinical and molecular characterization of two patients with overlapping de novo microdeletions in 2p14-p15 and mild mental retardation. European Journal of Medical Genetics. 54(1). 67–72.
8.
Kirchhoff, Maria, et al.. (2009). Increased nuchal translucency with normal karyotype: a follow‐up study of 100 cases supplemented with CGH and MLPA analyses. Ultrasound in Obstetrics and Gynecology. 34(6). 618–622.
9.
Hove, Hanne, et al.. (2008). A 15q24 microduplication, reciprocal to the recently described 15q24 microdeletion, in a boy sharing clinical features with 15q24 microdeletion syndrome patients. European Journal of Medical Genetics. 51(6). 520–526.
10.
Bisgaard, Anne‐Marie, et al.. (2007). Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata. Clinical Dysmorphology. 16(2). 109–112.
11.
Bache, Iben, Míriam Guitart, M.R. Caballı́n, et al.. (2007). Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome. European Journal of Human Genetics. 15(6). 711–713.
12.
Nygaard, Ulrikka, Jacob Larsen, Finn Wesenberg, et al.. (2006). Flow Cytometric DNA index, G-band Karyotyping, and Comparative Genomic Hybridization in Detection of High Hyperdiploidy in Childhood Acute Lymphoblastic Leukemia. Journal of Pediatric Hematology/Oncology. 28(3). 134–140.
13.
Gerdes, Tommy, Maria Kirchhoff, & Thue Bryndorf. (2005). Automatic analysis of multiplex ligation‐dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection). Electrophoresis. 26(22). 4327–4332.
14.
Lespinasse, James, et al.. (2004). De novo complex chromosomal rearrangements (CCR) involving chromosome 1, 5, and 6 resulting in microdeletion for 6q14 in a female carrier with psychotic disorder. American Journal of Medical Genetics Part A. 128A(2). 199–203.
15.
Wesenberg, Finn, Ólafur G. Jónsson, Erik Forestier, et al.. (2003). High‐resolution comparative genomic hybridisation yields a high detection rate of chromosomal aberrations in childhood acute lymphoblastic leukaemia. European Journal Of Haematology. 70(6). 363–372.
16.
Larsen, Jacob, Anne Marie Ottesen, Maria Kirchhoff, Claes Lundsteen, & Jørgen K. Larsen. (2001). High Resolution Comparative Genomic Hybridization Detects 7–8 Megabasepair Deletion in PCR Amplified DNA1. Analytical Cellular Pathology. 23(2). 61–64.
17.
Andersen, Mette Klarskov, Debes Hammershaimb Christiansen, Maria Kirchhoff, & J Pedersen-Bjergaard. (2001). Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy‐related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents. Genes Chromosomes and Cancer. 31(1). 33–41.
18.
Kirchhoff, Maria, Hanne Rose, Bodil Laub Petersen, et al.. (2001). Comparative genomic hybridization reveals non-random chromosomal aberrations in early preinvasive cervical lesions. Cancer Genetics and Cytogenetics. 129(1). 47–51.
19.
Kirchhoff, Maria, et al.. (2001). High resolution comparative genomic hybridisation in clinical cytogenetics. Journal of Medical Genetics. 38(11). 740–744.
20.
Larsen, Jacob, Maria Kirchhoff, Hanne Rose, et al.. (1999). Improved Sensitivity in Comparative Genomic Hybridization Analysis of DNA Heteroploid Cell Mixtures after Pre‐Enrichment of Subpopulations by Fluorescence Activated Cell Sorting. Analytical Cellular Pathology. 19(3-4). 119–124.
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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