Ricarda Flöttmann

729 total citations
12 papers, 163 citations indexed

About

Ricarda Flöttmann is a scholar working on Genetics, Molecular Biology and Developmental Biology. According to data from OpenAlex, Ricarda Flöttmann has authored 12 papers receiving a total of 163 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 4 papers in Developmental Biology. Recurrent topics in Ricarda Flöttmann's work include Genomic variations and chromosomal abnormalities (6 papers), Congenital limb and hand anomalies (4 papers) and Connective tissue disorders research (4 papers). Ricarda Flöttmann is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Congenital limb and hand anomalies (4 papers) and Connective tissue disorders research (4 papers). Ricarda Flöttmann collaborates with scholars based in Germany, Poland and Australia. Ricarda Flöttmann's co-authors include Stefan Mundlos, Malte Spielmann, Eva Klopocki, Sandra C. Doelken, R. Habenicht, Wiebke Hülsemann, Anna Sowińska‐Seidler, Denise Horn, Uwe Kornak and Siddaramappa J. Patil and has published in prestigious journals such as Journal of Medical Genetics, European Journal of Human Genetics and Orphanet Journal of Rare Diseases.

In The Last Decade

Ricarda Flöttmann

12 papers receiving 160 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ricarda Flöttmann Germany	8	111	95	45	19	13	12	163
Hugo Hernán Abarca-Barriga Peru	7	86 0.8×	88 0.9×	23 0.5×	15 0.8×	4 0.3×	30	159
B-W Gu China	6	208 1.9×	62 0.7×	52 1.2×	10 0.5×	3 0.2×	10	262
Dagmar Wahl Germany	5	106 1.0×	136 1.4×	8 0.2×	24 1.3×	5 0.4×	6	189
Lina Ramos Portugal	7	60 0.5×	80 0.8×	9 0.2×	31 1.6×	4 0.3×	22	127
Margaret Harr United States	10	79 0.7×	130 1.4×	5 0.1×	29 1.5×	13 1.0×	16	194
Lutz Pfeiffer Germany	6	69 0.6×	141 1.5×	6 0.1×	55 2.9×	2 0.2×	6	192
M. Doco‐Fenzy France	4	75 0.7×	94 1.0×	3 0.1×	9 0.5×	9 0.7×	8	138
Anne Bazin France	8	74 0.7×	119 1.3×	5 0.1×	90 4.7×	4 0.3×	16	195
Christina Kelbova Germany	7	65 0.6×	124 1.3×	4 0.1×	42 2.2×	3 0.2×	10	161
Carey McDougall United States	5	43 0.4×	46 0.5×	12 0.3×	7 0.4×	8 0.6×	11	89

Countries citing papers authored by Ricarda Flöttmann

Since Specialization

Citations

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

Fields of papers citing papers by Ricarda Flöttmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ricarda Flöttmann

This figure shows the co-authorship network connecting the top 25 collaborators of Ricarda Flöttmann. A scholar is included among the top collaborators of Ricarda Flöttmann 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 Ricarda Flöttmann. Ricarda Flöttmann 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

Danyel, Magdalena, Zhuo Cheng, Christine Jung, et al.. (2019). Differentiation of MISSLA and Fanconi anaemia by computer-aided image analysis and presentation of two novel MISSLA siblings. European Journal of Human Genetics. 27(12). 1827–1835. 6 indexed citations

Flöttmann, Ricarda, Malte Spielmann, Fabienne Escande, et al.. (2019). Split hand/foot malformation associated with 20p12.1 deletion: A case report. European Journal of Medical Genetics. 63(4). 103805–103805. 2 indexed citations

Türkmen, Seval, Malte Spielmann, Nilay Güneş, et al.. (2017). A Novel de novo FZD2 Mutation in a Patient with Autosomal Dominant Omodysplasia. Molecular Syndromology. 8(6). 318–324. 10 indexed citations

Kornak, Uwe, et al.. (2017). Novel splice mutation in LRP4 causes severe type of Cenani-Lenz syndactyly syndrome with oro-facial and skeletal symptoms. European Journal of Medical Genetics. 60(8). 421–425. 11 indexed citations

Flöttmann, Ricarda, Anna Sowińska‐Seidler, Julie Lavie, et al.. (2016). Duplication of PTHLH causes osteochondroplasia with a combined brachydactyly type E/A1 phenotype with disturbed bone maturation and rhizomelia. European Journal of Human Genetics. 24(8). 1132–1136. 7 indexed citations

Spielmann, Malte, Gotthold Barbi, Ricarda Flöttmann, et al.. (2016). Femoral facial syndrome associated with a de novo complex chromosome 2q37 rearrangement. American Journal of Medical Genetics Part A. 170(5). 1202–1207. 10 indexed citations

Neuhann, Teresa, Ricarda Flöttmann, Stefan Mundlos, et al.. (2016). A de novo 1q23.3-q24.2 deletion combined with a GORAB missense mutation causes a distinctive phenotype with cutis laxa. Journal of Human Genetics. 62(2). 325–328. 5 indexed citations

Enriquez, Annabelle, et al.. (2016). Recurrence of split hand/foot malformation, cleft lip/palate, and severe urogenital abnormalities due to germline mosaicism for TP63 mutation. American Journal of Medical Genetics Part A. 170(9). 2372–2376. 7 indexed citations

Flöttmann, Ricarda, Alexej Knaus, Tomasz Żemojtel, et al.. (2015). FGFR2 mutation in a patient without typical features of Pfeiffer syndrome – The emerging role of combined NGS and phenotype based strategies. European Journal of Medical Genetics. 58(8). 376–380. 5 indexed citations

10.

Flöttmann, Ricarda, Johannes Maximilian Wagner, Cynthia J. Curry, et al.. (2015). Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan type. Journal of Medical Genetics. 52(7). 476–483. 19 indexed citations

11.

Lohan, Silke B., Malte Spielmann, Sandra C. Doelken, et al.. (2014). Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas‐type polysyndactyly and Laurin‐Sandrow syndrome. Clinical Genetics. 86(4). 318–325. 48 indexed citations

12.

Tayebi, Naeimeh, Aleksander Jamsheer, Ricarda Flöttmann, et al.. (2014). Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families. Orphanet Journal of Rare Diseases. 9(1). 108–108. 33 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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