Stephanie Groß

1.5k total citations
12 papers, 934 citations indexed

About

Stephanie Groß is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Stephanie Groß has authored 12 papers receiving a total of 934 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Stephanie Groß's work include Genetic Syndromes and Imprinting (7 papers), Epigenetics and DNA Methylation (7 papers) and Prenatal Screening and Diagnostics (4 papers). Stephanie Groß is often cited by papers focused on Genetic Syndromes and Imprinting (7 papers), Epigenetics and DNA Methylation (7 papers) and Prenatal Screening and Diagnostics (4 papers). Stephanie Groß collaborates with scholars based in Germany, Switzerland and Netherlands. Stephanie Groß's co-authors include Bernhard Horsthemke, Karin Buiting, Bärbel Dittrich, Stuart Schwartz, Robert D. Nicholls, Shinji Saitoh, Christina Lich, Gabriele Gillessen‐Kaesbach, Osman El‐Maarri and Jürgen Neesen and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Stephanie Groß

11 papers receiving 894 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephanie Groß Germany	9	812	724	433	40	23	12	934
James M. Gabriel United States	6	455 0.6×	382 0.5×	202 0.5×	16 0.4×	28 1.2×	8	495
Luciano Calzari Italy	14	230 0.3×	338 0.5×	166 0.4×	17 0.4×	16 0.7×	38	519
Luís Fernández Spain	12	306 0.4×	261 0.4×	141 0.3×	10 0.3×	53 2.3×	23	565
A Moncla France	4	411 0.5×	318 0.4×	89 0.2×	11 0.3×	9 0.4×	6	467
Maria J. Mascari United States	6	414 0.5×	259 0.4×	150 0.3×	27 0.7×	112 4.9×	10	563
Surabhi Mulchandani United States	11	388 0.5×	131 0.2×	194 0.4×	20 0.5×	8 0.3×	17	474
Lisa Bowdler Australia	5	193 0.2×	359 0.5×	54 0.1×	24 0.6×	15 0.7×	7	468
Delanie B. Macedo Brazil	15	354 0.4×	374 0.5×	88 0.2×	13 0.3×	24 1.0×	22	723
Sarah Rickard United Kingdom	5	267 0.3×	291 0.4×	110 0.3×	21 0.5×	20 0.9×	7	385
N R Dennis United Kingdom	13	520 0.6×	242 0.3×	158 0.4×	12 0.3×	69 3.0×	23	654

Countries citing papers authored by Stephanie Groß

Since Specialization

Citations

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

Fields of papers citing papers by Stephanie Groß

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Groß

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

All Works

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12 of 12 papers shown

Kindermann, Ingrid, et al.. (2025). Determinants of reliability of self-reported height and weight and their impact on medication dosing: a cross-sectional study. BMJ Open. 15(4). e090020–e090020.

Gutman, Sharon A., et al.. (2018). Feasibility and Satisfaction of an Apartment Living Program for Homeless Adults With Mental Illness and Substance Use Disorder. Psychiatry. 81(3). 228–239. 8 indexed citations

Rath, Matthias, Stefanie Spiegler, Neetika Nath, et al.. (2016). Constitutional de novo and postzygotic mutations in isolated cases of cerebral cavernous malformations. Molecular Genetics & Genomic Medicine. 5(1). 21–27. 4 indexed citations

Zeschnigk, Michael, Marcel Martin, Karin Buiting, et al.. (2009). Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete. Human Molecular Genetics. 18(8). 1439–1448. 30 indexed citations

Neubauer, Bernd A., Stephanie Groß, & A. Hahn. (2008). Epilepsy in Childhood and Adolescence. Deutsches Ärzteblatt international. 105(17). 319–27; quiz 327. 15 indexed citations

Buiting, Karin, Deniz Kanber, José I. Martı́n-Subero, et al.. (2008). Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprintedDLK1/GTL2gene cluster. Human Mutation. 29(9). 1141–1146. 57 indexed citations

Böhringer, Stefan, et al.. (2006). Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15. European Journal of Human Genetics. 14(6). 752–758. 30 indexed citations

Buiting, Karin, Stephanie Groß, Christina Lich, et al.. (2003). Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect. The American Journal of Human Genetics. 72(3). 571–577. 208 indexed citations

Groß, Stephanie, et al.. (2000). Identification of a Testis-Specific Gene (C15orf2) in the Prader–Willi Syndrome Region on Chromosome 15. Genomics. 65(2). 174–183. 35 indexed citations

10.

Buiting, Karin, Shinji Saitoh, Stephanie Groß, et al.. (1995). Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15. Nature Genetics. 9(4). 395–400. 471 indexed citations

11.

Dittrich, Bärbel, Stephanie Groß, Karin Buiting, & Bernhard Horsthemke. (1993). An Ncil RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11 – 13. Human Molecular Genetics. 2(9). 1509–1509. 4 indexed citations

12.

Dittrich, Bärbel, Karin Buiting, Stephanie Groß, & Bernhard Horsthemke. (1993). Characterization of a methylation imprint in the Prader — Willi syndrome chromosome region. Human Molecular Genetics. 2(12). 1995–1999. 72 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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