Gabi Mücher

881 total citations
11 papers, 609 citations indexed

About

Gabi Mücher is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Gabi Mücher has authored 11 papers receiving a total of 609 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Gabi Mücher's work include Genetic and Kidney Cyst Diseases (11 papers), Renal and related cancers (9 papers) and Genetic Syndromes and Imprinting (4 papers). Gabi Mücher is often cited by papers focused on Genetic and Kidney Cyst Diseases (11 papers), Renal and related cancers (9 papers) and Genetic Syndromes and Imprinting (4 papers). Gabi Mücher collaborates with scholars based in Germany, United States and Finland. Gabi Mücher's co-authors include Klaus Zerres, Jutta Becker, Sabine Rudnik‐Schöneborn, Lisa M. Guay‐Woodford, C. Steinkamm, Markus Moser, Armin Pscherer, Joachim Weis, Reinhard Fässler and Reinhard Buettner and has published in prestigious journals such as Nature Genetics, Genes & Development and Biochemical and Biophysical Research Communications.

In The Last Decade

Gabi Mücher

11 papers receiving 596 citations

Peers

Countries citing papers authored by Gabi Mücher

Since Specialization

Citations

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

Fields of papers citing papers by Gabi Mücher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gabi Mücher

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

#	Work	Indexed citations
1	Prenatal Diagnosis of Autosomal Recessive Polycystic Kidney Disease (ARPKD): Molecular Genetics, Clinical Experience, and Fetal Morphology 1999 ·The Journal of Urology ·Klaus Zerres, Gabi Mücher, Jutta Becker, C. Steinkamm, (unknown), (unknown), Juhani Rapola, Riitta Salonen, Gregory G. Germino, Luiz F. Onuchic, Stefan Somlo, Ellis D. Avner, L. Harman, (unknown), Lisa M. Guay‐Woodford	11
2	Prenatal Diagnosis of Autosomal Recessive Polycystic Kidney Disease (ARPKD) 1999 ·The Journal of Urology ·Klaus Zerres, Gabi Mücher, Jutta Becker, C. Steinkamm, (unknown), (unknown), Juhani Rapola, Riitta Salonen, Gregory G. Germino, Luiz F. Onuchic, Stefan Somlo, Ellis D. Avner, L. Harman, (unknown), Lisa M. Guay‐Woodford	1
3	Autosomal recessive polycystic kidney disease 1998 ·Journal of Molecular Medicine ·Klaus Zerres, Sabine Rudnik‐Schöneborn, C. Steinkamm, Jutta Becker, Gabi Mücher	103
4	Fine Mapping of the Autosomal Recessive Polycystic Kidney Disease Locus (PKHD1) and the Genes MUT, RDS, CSNK2β, and GSTA1 at 6p21.1–p12 1998 ·Genomics ·Gabi Mücher, Jutta Becker, Michael Knapp, Reinhard Büttner, Markus Moser, Sabine Rudnik‐Schöneborn, Stefan Somlo, Gregory G. Germino, Luiz F. Onuchic, Ellis D. Avner, Lisa M. Guay‐Woodford, Klaus Zerres	34
5	Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology 1998 ·American Journal of Medical Genetics ·Klaus Zerres, Gabi Mücher, Jutta Becker, C. Steinkamm, Sabine Rudnik‐Schöneborn, Päivi Heikkilä, Juhani Rapola, Riitta Salonen, Gregory G. Germino, Luiz F. Onuchic, Stefan Somlo, Ellis D. Avner, L. Harman, (unknown), Lisa M. Guay‐Woodford	16
6	Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2β 1997 ·Genes & Development ·Markus Moser, Armin Pscherer, Christina Roth, Jutta Becker, Gabi Mücher, Klaus Zerres, Christa Dixkens, Joachim Weis, Lisa M. Guay‐Woodford, Reinhard Buettner, Reinhard Fässler	226
7	An Integrated Genetic and Physical Map of the Autosomal Recessive Polycystic Kidney Disease Region 1997 ·Genomics ·Xosé M. Lens, Luiz F. Onuchic, Guanqing Wu, Tomohito Hayashi, (unknown), Toshio Mochizuki, (unknown), (unknown), Gabi Mücher, Jutta Becker, (unknown), Ellis D. Avner, Lisa M. Guay‐Woodford, Klaus Zerres, Stefan Somlo, Gregory G. Germino	21
8	Autosomal recessive polycystic kidney disease 1996 ·Nephrology Dialysis Transplantation ·Klaus Zerres, Sabine Rudnik‐Schöneborn, C. Steinkamm, Gabi Mücher	11
9	Autosomal recessive polycystic kidney disease: clinical features and genetics. 1996 ·PubMed ·Klaus Zerres, Sabine Rudnik‐Schöneborn, Gabi Mücher	9
10	Fine Mapping of MEP1A, the Gene Encoding the α Subunit of the Metalloendopeptidase Meprin, to Human Chromosome 6p21 1995 ·Biochemical and Biophysical Research Communications ·W. Jiang, (unknown), Ellen K. Brundage, Gabi Mücher, Hans‐Ulrich Schildhaus, Klaus Zerres, Judith Bond	17
11	Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21–cen 1994 ·Nature Genetics ·Klaus Zerres, Gabi Mücher, L Bachner, (unknown), Thomas Eggermann, H Kääriäinen, Michael Knapp, Thomas Lennert, Joachim Misselwitz, K. E. von Mühlendahl, (unknown), Yves Pirson, Sabine Rudnik‐Schöneborn, V. Steinbicker, Brunhilde Wirth, K Schärer	160

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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