Anita Imm

1.4k total citations
14 papers, 658 citations indexed

About

Anita Imm is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anita Imm has authored 14 papers receiving a total of 658 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anita Imm's work include Genetic and Kidney Cyst Diseases (6 papers), Renal and related cancers (6 papers) and Pediatric Urology and Nephrology Studies (3 papers). Anita Imm is often cited by papers focused on Genetic and Kidney Cyst Diseases (6 papers), Renal and related cancers (6 papers) and Pediatric Urology and Nephrology Studies (3 papers). Anita Imm collaborates with scholars based in United States, Germany and Türkiye. Anita Imm's co-authors include Friedhelm Hildebrandt, Isabella Zalewski, Rainer Ruf, Anne Lichtenberger, Arno Fuchshuber, Ayşı̇n Bakkaloğlu, Michael Schultheiß, Thomas J. Neuhaus, Bettina E. Mucha and Stephanie M. Karle and has published in prestigious journals such as The Journal of Immunology, Kidney International and Journal of Clinical Microbiology.

In The Last Decade

Anita Imm

14 papers receiving 641 citations

Peers

Countries citing papers authored by Anita Imm

Since Specialization

Citations

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

Fields of papers citing papers by Anita Imm

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anita Imm

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

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

#	Work	Indexed citations
1	Prevalence of Capsular Serotype, Pilus Island Distribution, and Antibiotic Resistance in Pediatric and Adult Invasive Group B Streptococcus Isolates: Data From a Nationwide Prospective Surveillance Study in Germany 2020 ·The Pediatric Infectious Disease Journal ·(unknown), Angela Berg, (unknown), Anita Imm, Gérard Krause, (unknown), Reinhard Berner, Markus Hufnagel, (unknown)	12
2	Pseudodominant inheritance of nephronophthisis caused by a homozygous NPHP1 deletion 2011 ·Pediatric Nephrology ·Julia Hoefele, Ahmet Nayır, Moumita Chaki, Anita Imm, Susan J. Allen, Edgar A. Otto, Friedhelm Hildebrandt	18
3	Mutational analysis of theNPHP4 gene in 250 patients with nephronophthisis 2005 ·Human Mutation ·Julia Hoefele, Ralf Sudbrak, Richard Reinhardt, (unknown), Steffen Hennig, Anita Imm, (unknown), Boris Utsch, Massimo Attanasio, John F. O’Toole, Edgar A. Otto, Friedhelm Hildebrandt	46
4	Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2–q34.2 by total genome search for linkage 2005 ·Nephrology Dialysis Transplantation ·Matthias T. F. Wolf, Isabella Zalewski, Félix Claverie-Martı́n, Rainer Ruf, Dominik N. Müller, Hans Christian Hennies, (unknown), (unknown), Massimo Attanasio, (unknown), Anita Imm, Barbara Lucke, Boris Utsch, Edgar A. Otto, Peter Nürnberg, Víctor Manuel García Nieto, Friedhelm Hildebrandt	20
5	Patients with Mutations in NPHS2 (Podocin) Do Not Respond to Standard Steroid Treatment of Nephrotic Syndrome 2004 ·Journal of the American Society of Nephrology ·Rainer Ruf, Anne Lichtenberger, Stephanie M. Karle, Johannes‐Peter Haas, (unknown), Michael Schultheiß, Isabella Zalewski, Anita Imm, (unknown), Bettina E. Mucha, Arvind Bagga, Thomas J. Neuhaus, Arno Fuchshuber, Ayşı̇n Bakkaloğlu, Friedhelm Hildebrandt	282
6	Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome 2004 ·Kidney International ·Rainer Ruf, Michael Schultheiß, Anne Lichtenberger, Stephanie M. Karle, Isabella Zalewski, Bettina E. Mucha, Anne Schulze Everding, Thomas J. Neuhaus, Ludwig Patzer, Christian Plank, Johannes‐Peter Haas, Fatih Özaltın, Anita Imm, Arno Fuchshuber, Ayşı̇n Bakkaloğlu, Friedhelm Hildebrandt	89
7	A Gene Locus for Steroid-Resistant Nephrotic Syndrome with Deafness Maps to Chromosome 14q24.2 2003 ·Journal of the American Society of Nephrology ·Rainer Ruf, Matthias T. F. Wolf, Hans Christian Hennies, Barbara Lucke, (unknown), Verena Varnholt, Anne Lichtenberger, Andreas Pasch, Anita Imm, (unknown), Thomas Lennert, Arno Fuchshuber, Peter Nürnberg, Friedhelm Hildebrandt	6
8	Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisis 2001 ·Kidney International ·Friedhelm Hildebrandt, (unknown), Christopher Rensing, Regina C. Betz, Ülrike Sommer, Stefanie Birnbaum, Anita Imm, Heymut Omran, M. Leipoldt, Edgar A. Otto	29
9	Improved strategy for molecular genetic diagnostics in juvenile nephronophthisis 2001 ·American Journal of Kidney Diseases ·Erika Héninger, Edgar A. Otto, Anita Imm, Gianluca Caridi, Friedhelm Hildebrandt	11
10	A deletion distinct from the classical homologous recombination of juvenile nephronophthisis type 1 (NPH1) allows exact molecular definition of deletion breakpoints 2000 ·Human Mutation ·Edgar A. Otto, Regina C. Betz, Christopher Rensing, (unknown), Thomas Kuntzen, (unknown), Anita Imm, Friedhelm Hildebrandt	16
11	A deletion distinct from the classical homologous recombination of juvenile nephronophthisis type 1 (NPH1) allows exact molecular definition of deletion breakpoints 2000 ·Human Mutation ·Edgar A. Otto, Regina C. Betz, Christopher Rensing, (unknown), Thomas Kuntzen, (unknown), Anita Imm, Friedhelm Hildebrandt	2
12	Serotyping and electron microscopy studies of Staphylococcus aureus clinical isolates with monoclonal antibodies to capsular polysaccharide types 5 and 8 1987 ·Journal of Clinical Microbiology ·H. K. Hochkeppel, Dietmar G. Braun, W. A. Vischer, Anita Imm, (unknown), (unknown), R. Guggenheim, (unknown), A Boutonnier, Joëlle Fournier	123
13	Specificity of H-2-linked Ir gene control in mice: demonstration of T helper cells recognizing branched synthetic polypeptides in low responder mice. 1981 ·The Journal of Immunology ·H Stötter, Anita Imm, (unknown), Erwin Rüde	2
14	Specificity of H‐2‐linked Ir gene control in mice: Recognition of the core structure A–L in defined sequence analogues of (T,G)‐A–L 1979 ·European Journal of Immunology ·H Stötter, Anita Imm, (unknown), Erwin Rüde	2

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