Ingrid Bader

1.2k total citations
12 papers, 206 citations indexed

About

Ingrid Bader is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Ingrid Bader has authored 12 papers receiving a total of 206 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Ingrid Bader's work include Genetic and Kidney Cyst Diseases (3 papers), Genomics and Rare Diseases (2 papers) and Metabolism and Genetic Disorders (2 papers). Ingrid Bader is often cited by papers focused on Genetic and Kidney Cyst Diseases (3 papers), Genomics and Rare Diseases (2 papers) and Metabolism and Genetic Disorders (2 papers). Ingrid Bader collaborates with scholars based in Germany, Austria and Switzerland. Ingrid Bader's co-authors include Thomas Meitinger, Eckart Apfelstedt-Sylla, Bernd Wissinger, Alfons Meindl, Birgit Lorenz, Oliver Brandau, Helene Achatz, Martin Hergersberg, Johannes A. Mayr and Eugen Boltshauser and has published in prestigious journals such as Genome Research, Human Molecular Genetics and Investigative Ophthalmology & Visual Science.

In The Last Decade

Ingrid Bader

11 papers receiving 202 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ingrid Bader Germany	7	186	69	61	27	18	12	206
Mohammed E. El‐Asrag United Kingdom	10	153 0.8×	58 0.8×	51 0.8×	32 1.2×	11 0.6×	17	211
Saoud Tahsin Swafiri Spain	11	175 0.9×	98 1.4×	61 1.0×	21 0.8×	7 0.4×	15	252
Pooja Biswas United States	11	190 1.0×	69 1.0×	111 1.8×	30 1.1×	14 0.8×	25	232
Katherine Pohida United States	5	98 0.5×	63 0.9×	9 0.1×	20 0.7×	14 0.8×	6	143
Quansheng Xi United States	8	149 0.8×	38 0.6×	65 1.1×	50 1.9×	38 2.1×	14	199
Grace M. Wang United States	8	88 0.5×	40 0.6×	22 0.4×	12 0.4×	4 0.2×	12	158
Natsue Omi Japan	8	143 0.8×	38 0.6×	187 3.1×	32 1.2×	4 0.2×	12	295
Laura Steenpaß Germany	9	205 1.1×	112 1.6×	40 0.7×	8 0.3×	11 0.6×	28	279
Keng Wee Teik Malaysia	8	69 0.4×	72 1.0×	13 0.2×	14 0.5×	14 0.8×	11	131
Phillip Gonzalez Brazil	4	316 1.7×	84 1.2×	85 1.4×	5 0.2×	43 2.4×	8	352

Countries citing papers authored by Ingrid Bader

Since Specialization

Citations

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

Fields of papers citing papers by Ingrid Bader

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingrid Bader

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

Beck‐Woedl, Stefanie, Katalin Komlósi, Matthias Eckenweiler, et al.. (2023). Novel homozygous LAMB1 in‐frame deletion in a pediatric patient with brain anomalies and cerebrovascular event. American Journal of Medical Genetics Part A. 191(10). 2656–2663. 1 indexed citations

Bader, Ingrid, Martin A. Rooimans, Anneke B. Oostra, et al.. (2022). Biallelic BUB1 mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation. Sapientia (Algarve University). 15 indexed citations

Bader, Ingrid, Michael Freilinger, Franz Landauer, et al.. (2022). A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathy. Orphanet Journal of Rare Diseases. 17(1). 279–279. 2 indexed citations

Epting, Daniel, Eva L. Decker, Elisabeth Ott, et al.. (2022). The ciliary transition zone protein TMEM218 synergistically interacts with the NPHP module and its reduced dosage leads to a wide range of syndromic ciliopathies. Human Molecular Genetics. 31(14). 2295–2306. 5 indexed citations

Schröder, Simone, Yun Li, Gökhan Yigit, et al.. (2020). Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia. Genetics in Medicine. 23(2). 341–351. 10 indexed citations

Bader, Ingrid, et al.. (2020). Severe syndromic ID and skewed X-inactivation in a girl with NAA10 dysfunction and a novel heterozygous de novo NAA10 p.(His16Pro) variant - a case report. BMC Medical Genetics. 21(1). 153–153. 14 indexed citations

Wortmann, Saskia B., Johannes Koch, Christian Rauscher, et al.. (2018). Next-Generation-Sequenzierung – Next-Generation-Qualität in der Pädiatrie. Pädiatrie & Pädologie. 53(6). 278–283.

Koch, J., Johannes A. Mayr, Benjamin J.S. al-Haddad, et al.. (2017). Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations. Neuropediatrics. 48(S 01). S1–S45. 1 indexed citations

Bader, Ingrid, Eva L. Decker, Johannes A. Mayr, et al.. (2016). MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum. European Journal of Medical Genetics. 59(8). 386–391. 13 indexed citations

10.

Zweier, Christiane, Olaf Rittinger, Ingrid Bader, et al.. (2014). Females with de novo aberrations in PHF6: Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(3). 290–301. 20 indexed citations

11.

Bader, Ingrid, Oliver Brandau, Helene Achatz, et al.. (2003). X-linked Retinitis Pigmentosa:RPGRMutations in Most Families with Definite X Linkage and Clustering of Mutations in a Short Sequence Stretch of Exon ORF15. Investigative Ophthalmology & Visual Science. 44(4). 1458–1458. 101 indexed citations

12.

Schindelhauer, Dirk, Heide Hellebrand, Ingrid Bader, et al.. (1996). Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich interval.. Genome Research. 6(11). 1056–1069. 24 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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