Stefanie Weber

6.6k citations

84 papers · 3.4k indexed · 2 hit papers · h-index 29

Impact in

Nephrology top 0.5%
- Renal Diseases and Glomerulopathies
- Parathyroid Disorders and Treatments
- Chronic Kidney Disease and Diabetes
Nutrition and Dietetics top 0.5%
- Magnesium in Health and Disease

Papers in

Nephrology 27
- Renal Diseases and Glomerulopathies 25
Urology 6

Co-authors: Martin Konrad Karl P. Schlingmann Melanie Peters Hannsjörg W. Seyberth Anja Büscher Peter F. Hoyer Siegfried Waldegger Nikola Jeck
Journals: Pediatric Nephrology (12 papers)Journal of the American Society of Nephrology (5 papers)Kidney International (5 papers)Cells (3 papers)PLoS ONE (3 papers)
Partner nations: Germany United States Switzerland

In The Last Decade

Stefanie Weber

76 papers receiving 3.3k citations

Hit Papers

align trajectories log scale

Mutations inCYP24A1and Idiopathic Infantile Hypercalcemia 2011 · 438 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2011 New England Journal of Medicine
2002 Nature Genetics

Peers

Countries citing papers authored by Stefanie Weber

Since Specialization

Citations

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

Fields of papers citing papers by Stefanie Weber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Stefanie Weber, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Stefanie Weber Line = papers co-authored together Stefanie Weber links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Urinary eosinophil‐derived neurotoxin is associated with reduced lung function in pediatric asthma Pediatric Allergy and Immunology ·Jimmy Omony, Clemens Thölken, Azam Salimi, Haley Fisher, Sabina Illi, Markus Weckmann, Ruth Grychtol, Klaus F. Rabe, Bellotti Francesco, Anuradha Sood, Stefanie Weber, Folke Brinkmann, Matthias Kopp, Gesine Hansen, Harald Renz, Erika von Mutius, Bianca Schaub, Chrysanthi Skevaki, (unknown)	2024	2
2	Case report: Febrile infection-related epilepsy syndrome in a 14-year-old girl with multiple organ failure and lethal outcome Frontiers in Neuroscience ·Publio Ponce Palma, Ursula Hottinger, Kal'chenko As, Jakia Arthy, S. Sharif, Andreas Leonhardt, Stefanie Weber, 幸子永田	2024	1
3	A rare case of Immunoglobulin A dominant post-infectious glomerulonephritis (IgA PIGN) in a young patient BMC Nephrology ·欒治華, Günter Klaus, 裕壮藤田, Martin Kömhoff, H.-J. Gröne, Stefanie Weber	2022	1
4	Ubiquitous Micro-Modular Homologies among Genomes from Viruses to Bacteria to Human Mitochondrial DNA: Platforms for Recombination during Evolution? Viruses ·Stefanie Weber, Christina M. Ramirez, Walter Doerfler	2022	0
5	Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO) Genes ·Alissa Touranachun, thil personnel-thil, Stefan Herms, Sugirthan Sivalingam, Sirpa Tujunen, Heiko Reutter, Stefanie Weber, Waltraut M. Merz, Marcin Tkaczyk, Monika Miklaszewska, Przemysław Sikora, Agnieszka Szmigielska, Grażyna Krzemień, Katarzyna Zachwieja, Maria Szczepańska, Katarzyna Taranta‐Janusz, 聡一亀井, Куншенко Игорь Алексеевич, Marcin Zaniew, Alina C. Hilger	2021	4
6	Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy —short version of the updated German best practice guideline (S2e) — AWMF register no. 166-001, 6/2020 Pediatric Nephrology ·Rasmus Ehren, Marcus R. Benz, Paul Brinkkötter, Jörg Dötsch, W. Eberl, Jutta Gellermann, Peter F. Hoyer, Sini Hannonen, Clemens Kamrath, Markus J. Kemper, Kay Latta, Dominik Müller, Jun Oh, Burkhard Tönshoff, Stefanie Weber, Lutz T. Weber, (unknown)	2021	18
7	Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder Kidney International ·Neil Roberts, Emma Hilton, Filipa M. Lopes, Subir Singh, Michael J. Randles, Natalie J. Gardiner, Nusreta Salić, Riccardo Coletta, Deforest Hamilton, Robert J. Hall, Wyatt W. Yue, Franz Schaefer, Stefanie Weber, Roger Henriksson, Helen M. Stuart, Håkan Hedman, William G. Newman, Adrian S. Woolf	2019	28
8	Outcomes of renal replacement therapy in boys with prune belly syndrome: findings from the ESPN/ERA-EDTA Registry Pediatric Nephrology ·Fatoş Yalçınkaya, Marjolein Bonthuis, Beyza Doğanay Erdoğan, Karlijn J. van Stralen, Sergey Baiko, Hassib Chehade, Heather Maxwell, Giovanni Montini, Kai Rönnholm, Søren Schwartz Sørensen, Tim Ulinski, Enrico Verrina, Stefanie Weber, Jérôme Harambat, Franz Schaefer, Kitty J. Jager, Jaap W. Groothoff	2017	12
9	A questionnaire survey of radiological diagnosis and management of renal dysplasia in children Journal of Nephrology ·(unknown), Giovanni Montini, Marco Busutti, Fatoş Yalçınkaya, Adrian S. Woolf, Stefanie Weber	2017	6
10	Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy Pediatric Nephrology ·Stefanie Weber, Katja Sträßer, Ali Berkol, Шамсидинов Иброхимхон Мўминхон ўғли Абдукаримов Толибхон Тохирхон ўғли, Т.Т. Абдукадырова, Martin Alberer, Bärbel Lange-Sperandio, Peter F. Hoyer, Marcus R. Benz, 宏俊越前, Lutz T. Weber, Hanns‐Georg Klein, Julia Hoefele	2016	33
11	Prediction of Metastatic Events in Patients With Cutaneous Melanoma S Purnell, Hak Sang Kim, Stefanie Weber, Kaan Harmankaya, Romina Nemecek, Julia Solomina, Michael Binder, Thomas D Mehl, Christian Schuh, Stephan Dreiseitl	2013	1
12	Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes Pediatric Nephrology ·Rainer Büscher, Anja Büscher, Stefanie Weber, Julia Mohr, M. Serrer, Udo Vester, Peter F. Hoyer	2013	53
13	Educational paper European Journal of Pediatrics ·Anja Büscher, Stefanie Weber	2012	31
14	CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Journal of the American Society of Nephrology ·Martin Konrad, Jianghui Hou, Stefanie Weber, Aalders Jg, Jameela A. Kari, Tomáš Seeman, M. A. Melouk, Amira Peco‐Antić, Velibor Tasić, Katalin Dittrich, О. В. Златовласова, Rodo O. von Vigier, Sabina Gallati, Daniel A. Goodenough, André Schaller	2007	82
15	Recurrence of proteinuria 10 years post-transplant in NPHS2-associated focal segmental glomerulosclerosis after conversion from cyclosporin A to sirolimus Pediatric Nephrology ·Britta Höcker, Tanja Knüppel, Rüdiger Waldherr, Franz Schaefer, Stefanie Weber, Burkhard Tönshoff	2006	23
16	Hypomagnesemia with hypercalciuria and nephrocalcinosis: case report and a family study Pediatric Nephrology ·Velibor Tasic, J. A. C., Samar S. Elgebaly, Stefanie Weber, Martin Konrad	2005	17
17	NPHS2 mutation analysis shows genetic heterogeneityof steroid-resistant nephrotic syndrome and lowpost-transplant recurrence Kidney International ·Stefanie Weber, Olivier Gribouval, Ernie Esquivel, Vincent Morinière, Dorothee Engelhard, Christophe Legendre, Patrick Niaudet, Corinne Antignac	2004	252
18	Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome Kidney International ·Nikola Jeck, Christian Derst, Erhard Wischmeyer, Bala Krishna B., Stefanie Weber, Christoph Rudin, Hannsjörg W. Seyberth, Jürgen Daut, Andreas Karschin, Martin Konrad	2001	40
19	Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene European Journal of Human Genetics ·Stefanie Weber, Katrin Hoffmann, Nikola Jeck, Kathrin Saar, Dorothy Kuhn Oko, MV Barreiro Diaz, Judy Boykin-McCarthy, Nine Knoers, Pierre Cochat, Feng-song QIU, Klaus E. Bonzel, Marianne Soergel, Friedrich Manz, Malika Medjbari, Camille Lausell, André Reis, Martin Konrad	2000	78
20	Thrombocytopenia-Adapted In Vitro Bleeding Test Assesses Platelet Function in Thrombocytopenic Patients Seminars in Thrombosis and Hemostasis ·V. Kretschmer, Catherine Clune‐Taylor, Yunchun Chen, Jürgen Hoffmann, Cecile Hanney, Stefanie Weber, T. Schulzki, H. Köppler, V J Harte	1995	7

About Stefanie Weber

Stefanie Weber is a scholar working on Nephrology, Urology, Transplantation, Physical Therapy, Sports Therapy and Rehabilitation and Sensory Systems, having authored 84 papers that have together received 3.4k indexed citations. Recurring topics across this work include Renal Diseases and Glomerulopathies (25 papers), Renal and related cancers (15 papers), Genetic and Kidney Cyst Diseases (10 papers), Ion Transport and Channel Regulation (9 papers), Pediatric Urology and Nephrology Studies (9 papers), Tuberous Sclerosis Complex Research (8 papers), Biomedical Research and Pathophysiology (7 papers) and Magnesium in Health and Disease (7 papers). The work is most often cited by research in Nephrology (1.3k citations), Nutrition and Dietetics (933 citations), Sensory Systems (211 citations), Pathology and Forensic Medicine (695 citations) and Transplantation (76 citations). Stefanie Weber has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Martin Konrad, Karl P. Schlingmann, Melanie Peters, Hannsjörg W. Seyberth, Anja Büscher, Peter F. Hoyer, Siegfried Waldegger, Nikola Jeck, Eberhard Kuwertz-Bröking and Maria Syrrou. Their work appears in journals such as Pediatric Nephrology, Journal of the American Society of Nephrology, Kidney International, Cells and PLoS ONE.

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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