Christine Fauth

4.5k total citations · 1 hit paper
66 papers, 2.3k citations indexed

About

Christine Fauth is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Christine Fauth has authored 66 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 32 papers in Molecular Biology and 17 papers in Plant Science. Recurrent topics in Christine Fauth's work include Genomic variations and chromosomal abnormalities (27 papers), Chromosomal and Genetic Variations (17 papers) and Prenatal Screening and Diagnostics (12 papers). Christine Fauth is often cited by papers focused on Genomic variations and chromosomal abnormalities (27 papers), Chromosomal and Genetic Variations (17 papers) and Prenatal Screening and Diagnostics (12 papers). Christine Fauth collaborates with scholars based in Austria, Germany and United States. Christine Fauth's co-authors include Michael R. Speicher, Thomas Cremer, Roland Eils, Kaan Saracoglu, Andreas Bolzer, Stefan Müller, Christoph Cremer, Irina Solovei, Gregor Kreth and Daniela Koehler and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Cell Biology and PLoS Biology.

In The Last Decade

Christine Fauth

64 papers receiving 2.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Three-Dimensional Maps of All Chromosomes in Human Male Fibroblast Nuclei and Prometaphase Rosettes

2005 611 citations Kaan Saracoglu, Christine Fauth et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christine Fauth Austria	22	1.5k	790	522	234	211	66	2.3k
H F Willard United States	22	1.2k 0.8×	804 1.0×	545 1.0×	112 0.5×	124 0.6×	28	1.8k
Francesca Cole United States	20	2.2k 1.5×	636 0.8×	298 0.6×	258 1.1×	73 0.3×	30	2.5k
Eugene M. Rinchik United States	32	1.9k 1.3×	1.1k 1.4×	222 0.4×	350 1.5×	108 0.5×	82	2.6k
Gerard Merkx Netherlands	25	1.6k 1.0×	570 0.7×	219 0.4×	160 0.7×	158 0.7×	52	2.2k
W. Roy Breg United States	18	1.1k 0.7×	815 1.0×	238 0.5×	82 0.4×	149 0.7×	26	2.0k
Antony E. Shrimpton United States	21	842 0.6×	531 0.7×	219 0.4×	334 1.4×	93 0.4×	51	2.0k
Elena Prigmore United Kingdom	18	742 0.5×	758 1.0×	225 0.4×	93 0.4×	164 0.8×	27	1.4k
Kyoichi Isono Japan	29	2.2k 1.5×	357 0.5×	249 0.5×	135 0.6×	53 0.3×	58	2.6k
Elizabeth Nanthakumar United States	11	1.1k 0.7×	1.5k 1.8×	317 0.6×	115 0.5×	42 0.2×	12	2.9k
Anja Ebert Austria	22	2.5k 1.7×	340 0.4×	424 0.8×	83 0.4×	62 0.3×	28	3.5k

Countries citing papers authored by Christine Fauth

Since Specialization

Citations

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

Fields of papers citing papers by Christine Fauth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christine Fauth. 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 Christine Fauth. The network helps show where Christine Fauth may publish in the future.

Co-authorship network of co-authors of Christine Fauth

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

All Works

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20 of 20 papers shown

Fauth, Christine, et al.. (2024). Treatment of psychiatric comorbidities and interaction patterns in Coffin‐Siris syndrome: A case report of a 4‐year‐old girl. SHILAP Revista de lepidopterología. 12(2). e8230–e8230. 1 indexed citations

Fauth, Christine, et al.. (2022). Generation of the human induced pluripotent stem cell line (IBKMOLi002-A) from PBMCs of a patient carrying the heterozygous L271H mutation of the voltage-gated calcium channel subunit Cav1.3-encoding CACNA1D gene. Stem Cell Research. 61. 102784–102784. 1 indexed citations

Fauth, Christine, Katharina Steindl, Annick Toutain, et al.. (2015). A recurrent germline mutation in the PIGA gene causes Simpson‐Golabi‐Behmel syndrome type 2. American Journal of Medical Genetics Part A. 170(2). 392–402. 30 indexed citations

Deutschmann, Andrea, et al.. (2014). Genotype-based databases for variants causing rare diseases. Gene. 550(1). 136–140. 10 indexed citations

Hackmann, Karl, Jens Schallner, Evelin Schröck, et al.. (2013). Severe intellectual disability, West syndrome, Dandy–Walker malformation, and syndactyly in a patient with partial tetrasomy 17q25.3. American Journal of Medical Genetics Part A. 161(12). 3144–3149. 13 indexed citations

Revençu, Nicole, Birgit Krabichler, Véronique Beauloye, et al.. (2013). Severe growth retardation, delayed bone age, and facial dysmorphism in two patients with microduplications in 2p16 → p22. American Journal of Medical Genetics Part A. 161(12). 3176–3181. 17 indexed citations

Rostásy, Kevin, Christine Fauth, Kurt Gautsch, et al.. (2012). Modification of risk for cancer as a coincidental finding in DNA array investigation. Clinical Genetics. 83(3). 284–287. 1 indexed citations

Großmann, Vera, Martina Höckner, Houda Karmous‐Benailly, et al.. (2010). Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite‐mediated haplotype analysis. Clinical Genetics. 78(6). 548–553. 24 indexed citations

Fauth, Christine, Hildegard Kehrer‐Sawatzki, Andrea Zaťková, et al.. (2009). Two sporadic spinal neurofibromatosis patients with malignant peripheral nerve sheath tumour. European Journal of Medical Genetics. 52(6). 409–414. 6 indexed citations

10.

Höckner, Martina, Barbara Utermann, Martin Erdel, et al.. (2008). Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman. American Journal of Medical Genetics Part A. 146A(7). 925–929. 14 indexed citations

11.

Fauth, Christine, Susan Gribble, Keith Porter, et al.. (2006). Micro-array analyses decipher exceptional complex familial chromosomal rearrangement. Human Genetics. 119(1-2). 145–153. 17 indexed citations

12.

Utermann, Barbara, Mariluce Riegel, Dru F. Leistritz, et al.. (2006). Pre‐ and postnatal findings in trisomy 17 mosaicism. American Journal of Medical Genetics Part A. 140A(15). 1628–1636. 17 indexed citations

13.

Kotzot, Dieter, et al.. (2005). Del(18)(q12.2q21.1) caused by a paternal sister chromatid rearrangement in a developmentally delayed girl. American Journal of Medical Genetics Part A. 135A(3). 304–307. 11 indexed citations

14.

Fauth, Christine, et al.. (2004). Order of genetic events is critical determinant of aberrations in chromosome count and structure. Genes Chromosomes and Cancer. 40(4). 298–306. 20 indexed citations

15.

Eggermann, Thomas, Klaus Zerres, Dirk Anhuf, et al.. (2004). Somatic mosaicism for a heterozygous deletion of the survival motor neuron (SMN1) gene. European Journal of Human Genetics. 13(3). 309–313. 12 indexed citations

16.

Saracoglu, Kaan, Jill M. Brown, Robert E. Kearney, et al.. (2001). New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization. Cytometry. 44(1). 7–15. 33 indexed citations

17.

Langer, Sabine, Christine Fauth, Mariano Rocchi, Jan Murken, & Michael R. Speicher. (2001). AcroM fluorescent in situ hybridization analyses of marker chromosomes. Human Genetics. 109(2). 152–158. 16 indexed citations

18.

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

19.

Meyer, B.-U., et al.. (1994). Functional organisation of corticonuclear pathways to motoneurones of lower facial muscles in man. Experimental Brain Research. 101(3). 465–72. 51 indexed citations

20.

Fauth, Christine, et al.. (1991). Establishment of Renal Cell Lines Derived from S<sub>2</sub> Segments of the Proximal Tubule. Kidney & Blood Pressure Research. 14(3). 128–139. 5 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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