Ina Hainmann

643 total citations
11 papers, 248 citations indexed

About

Ina Hainmann is a scholar working on Molecular Biology, Hematology and Cell Biology. According to data from OpenAlex, Ina Hainmann has authored 11 papers receiving a total of 248 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Hematology and 2 papers in Cell Biology. Recurrent topics in Ina Hainmann's work include Fungal and yeast genetics research (4 papers), Platelet Disorders and Treatments (2 papers) and Cancer-related gene regulation (2 papers). Ina Hainmann is often cited by papers focused on Fungal and yeast genetics research (4 papers), Platelet Disorders and Treatments (2 papers) and Cancer-related gene regulation (2 papers). Ina Hainmann collaborates with scholars based in Germany, United States and Netherlands. Ina Hainmann's co-authors include Barbara Zieger, Ellen van Drunen, Gudmar Lönnerholm, Jules P.P. Meijerink, Elisabeth R. van Wering, Anne R. M. von Bergh, Rob Pieters, H. Berna Beverloo, Laura J. C. M. van Zutven and Jerry Ware and has published in prestigious journals such as Blood, FEBS Letters and Gene.

In The Last Decade

Ina Hainmann

11 papers receiving 245 citations

Peers

Ina Hainmann

MB

HEMAT

CB

PHEOH

PRM

Kirstin Sandrock Germany

Martina Moras France

Lars Klenner Germany

Indra Gusti Mansur Indonesia

Hector Huerga Encabo United Kingdom

Rajesh Bakshi Switzerland

Daniela Cambria Italy

Darah Christie Canada

Hee Kyung Kim United States

Jinny Paul United States

Kirstin Sandrock Germany

Ina Hainmann

162 ×1.1

MB

73 ×1.0

HEMAT

64 ×1.1

CB

6 ×0.2

PHEOH

23 ×0.9

PRM

Citations per year, relative to Ina Hainmann Ina Hainmann (= 1×) peers Kirstin Sandrock

Countries citing papers authored by Ina Hainmann

Since Specialization

Citations

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

Fields of papers citing papers by Ina Hainmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ina Hainmann

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

All Works

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11 of 11 papers shown

1.

Włodarski, Marcin W., Lydie Da Costa, Marie-Françoise O’Donohue, et al.. (2018). Recurring mutations in RPL15 are linked to hydrops fetalis and treatment independence in Diamond-Blackfan anemia. Haematologica. 103(6). 949–958. 17 indexed citations

2.

Włodarski, Marcin W., Lydie Da Costa, Marie-Françoise O’Donohue, et al.. (2017). Mutations in Ribosomal Protein Genes L9 and L15 Link to DBA with Specific Clinical Phenotypes. Blood. 130. 1172–1172. 1 indexed citations

3.

Bartsch, Ingrid, Kirstin Sandrock, François Lanza, et al.. (2011). Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay. Thrombosis and Haemostasis. 106(9). 475–483. 30 indexed citations

4.

Grainger, John D., Paula Bolton‐Maggs, Bertrand Godeau, et al.. (2010). Diagnosis and management of chronic ITP: comments from an ICIS expert group. Annals of Hematology. 89(S1). 11–17. 13 indexed citations

5.

Sandrock, Kirstin, et al.. (2010). Compound Heterozygous Mutations in 2 Siblings with Hermansky-Pudlak Syndrome Type 1 (HPS1). Klinische Pädiatrie. 222(3). 168–174. 10 indexed citations

6.

Hainmann, Ina, Johannes Oldenburg, A. Pavlova, Andrea Superti‐Furga, & Barbara Zieger. (2009). Identification of a novel factor X deletion in combination with a missense mutation in the F10 gene - Genotype-phenotype correlation in a girl with severe factor X deficiency.. PubMed. 29(2). 184–6. 3 indexed citations

7.

Bergh, Anne R. M. von, Ellen van Drunen, Elisabeth R. van Wering, et al.. (2006). High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9. Genes Chromosomes and Cancer. 45(8). 731–739. 59 indexed citations

8.

Bauer, Heike, et al.. (2004). The novel human platelet septin SEPT8 is an interaction partner of SEPT4. Thrombosis and Haemostasis. 91(5). 959–966. 27 indexed citations

9.

Hainmann, Ina, et al.. (2003). Isolation of new splice isoforms, characterization and expression analysis of the human septin SEPT8 (KIAA0202). Gene. 312. 313–320. 23 indexed citations

10.

Hainmann, Ina, et al.. (2002). Human septin–septin interaction: CDCrel‐1 partners with KIAA0202. FEBS Letters. 519(1-3). 169–172. 28 indexed citations

11.

Zieger, Barbara, et al.. (2000). Characterization and expression analysis of two human septin genes, PNUTL1 and PNUTL2. Gene. 261(2). 197–203. 37 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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