Christiane Spaich

1.0k total citations
8 papers, 432 citations indexed

About

Christiane Spaich is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Christiane Spaich has authored 8 papers receiving a total of 432 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Christiane Spaich's work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic Syndromes and Imprinting (1 paper). Christiane Spaich is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic Syndromes and Imprinting (1 paper). Christiane Spaich collaborates with scholars based in Germany, Switzerland and Spain. Christiane Spaich's co-authors include Axel Bohring, Peter Wieacker, Claudia M. Haase, Ute Hehr, Susanne Ledig, Albrecht Röpke, Saadettin Sel, Thomas Stamm, Max Schubach and Deborah Bartholdi and has published in prestigious journals such as The American Journal of Human Genetics, The Journal of Pediatrics and European Journal of Human Genetics.

In The Last Decade

Christiane Spaich

8 papers receiving 427 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christiane Spaich Germany 8 304 269 59 37 28 8 432
Esther Geán Spain 13 294 1.0× 258 1.0× 21 0.4× 40 1.1× 14 0.5× 20 434
V Der Kaloustian United States 9 296 1.0× 149 0.6× 7 0.1× 44 1.2× 19 0.7× 14 553
H.-J. Lüdecke Germany 9 211 0.7× 169 0.6× 43 0.7× 18 0.5× 3 0.1× 10 345
Shelly Oommen United Kingdom 10 280 0.9× 116 0.4× 53 0.9× 17 0.5× 4 0.1× 13 371
Britta Fiebig Germany 13 489 1.6× 134 0.5× 62 1.1× 45 1.2× 21 0.8× 21 622
A E Bale United States 8 450 1.5× 171 0.6× 91 1.5× 16 0.4× 164 5.9× 8 521
A Baxová Czechia 10 243 0.8× 246 0.9× 10 0.2× 49 1.3× 3 0.1× 40 416
Jeong-Oh Shin South Korea 14 349 1.1× 222 0.8× 18 0.3× 30 0.8× 3 0.1× 30 492
Monica Hrynchak Canada 13 124 0.4× 178 0.7× 11 0.2× 7 0.2× 7 0.3× 25 368
Oscar F. Chacón‐Camacho Mexico 12 348 1.1× 211 0.8× 5 0.1× 43 1.2× 12 0.4× 62 533

Countries citing papers authored by Christiane Spaich

Since Specialization
Citations

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

Fields of papers citing papers by Christiane Spaich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christiane Spaich

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

All Works

8 of 8 papers shown
1.
Döcker, Dennis, Max Schubach, Moritz Menzel, et al.. (2014). Germline PTPN11 and somatic PIK3CA variant in a boy with megalencephaly-capillary malformation syndrome (MCAP) - pure coincidence?. European Journal of Human Genetics. 23(3). 409–412. 11 indexed citations
2.
Döcker, Dennis, Max Schubach, Moritz Menzel, et al.. (2013). Further delineation of the SATB2 phenotype. European Journal of Human Genetics. 22(8). 1034–1039. 68 indexed citations
3.
Spengler, Sabrina, Matthias Begemann, Nadina Ortiz Brüchle, et al.. (2012). Molecular Karyotyping as a Relevant Diagnostic Tool in Children with Growth Retardation with Silver-Russell Features. The Journal of Pediatrics. 161(5). 933–942.e1. 23 indexed citations
4.
Azzarello‐Burri, Silvia, Gabriele Gillessen‐Kaesbach, Peter Meinecke, et al.. (2009). Goltz–Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap. European Journal of Human Genetics. 17(10). 1207–1215. 28 indexed citations
5.
Vandewalle, Joke, Hilde Van Esch, Karen Govaerts, et al.. (2009). Dosage-Dependent Severity of the Phenotype in Patients with Mental Retardation Due to a Recurrent Copy-Number Gain at Xq28 Mediated by an Unusual Recombination. The American Journal of Human Genetics. 85(6). 809–822. 57 indexed citations
6.
Bohring, Axel, Thomas Stamm, Christiane Spaich, et al.. (2009). WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes. The American Journal of Human Genetics. 85(1). 97–105. 156 indexed citations
7.
Erdogan, Fikret, Reinhard Ullmann, Wei Chen, et al.. (2006). Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome “tiling path” BAC array in a girl with heart defect, cleft palate, and developmental delay. American Journal of Medical Genetics Part A. 143A(2). 172–178. 46 indexed citations
8.
Bohring, Axel, Margherita Silengo, Margherita Lerone, et al.. (1999). Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?. American Journal of Medical Genetics. 85(5). 438–446. 43 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Esther Geán Breakdown of academic impact, for papers by V Der Kaloustian Breakdown of academic impact, for papers by H.-J. Lüdecke Breakdown of academic impact, for papers by Shelly Oommen Breakdown of academic impact, for papers by Britta Fiebig Breakdown of academic impact, for papers by A E Bale Breakdown of academic impact, for papers by A Baxová Breakdown of academic impact, for papers by Jeong-Oh Shin Breakdown of academic impact, for papers by Monica Hrynchak Breakdown of academic impact, for papers by Oscar F. Chacón‐Camacho
Rankless by CCL
2026