Ulrike Schwarze

9.1k total citations · 1 hit paper
64 papers, 4.2k citations indexed

About

Ulrike Schwarze is a scholar working on Genetics, Rheumatology and Molecular Biology. According to data from OpenAlex, Ulrike Schwarze has authored 64 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 17 papers in Rheumatology and 16 papers in Molecular Biology. Recurrent topics in Ulrike Schwarze's work include Connective tissue disorders research (50 papers), Cell Adhesion Molecules Research (10 papers) and Dermatological and Skeletal Disorders (7 papers). Ulrike Schwarze is often cited by papers focused on Connective tissue disorders research (50 papers), Cell Adhesion Molecules Research (10 papers) and Dermatological and Skeletal Disorders (7 papers). Ulrike Schwarze collaborates with scholars based in United States, Germany and Canada. Ulrike Schwarze's co-authors include Peter H. Byers, Melanie Pepin, Andrea Superti‐Furga, Dru F. Leistritz, David R. Eyre, Elizabeth M. Petty, James M. Pace, David W. Russell, Jayne A. Goldstein and Lynne T. Smith and has published in prestigious journals such as Science, New England Journal of Medicine and Cell.

In The Last Decade

Ulrike Schwarze

63 papers receiving 4.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Clinical and Genetic Features of Ehlers–Danlos Syndrome Type IV, the Vascular Type

2000 814 citations Melanie Pepin, Ulrike Schwarze et al. New England Journal of Medicine profile →

Peers

Countries citing papers authored by Ulrike Schwarze

Since Specialization

Citations

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

Fields of papers citing papers by Ulrike Schwarze

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrike Schwarze

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Multidisciplinary hybrid approach to management of a thoracoabdominal aneurysm in a patient with both Loeys-Dietz and vascular Ehlers-Danlos syndrome 2024 ·Journal of Vascular Surgery Cases and Innovative Techniques ·(unknown), (unknown), Scott DeRoo, Ulrike Schwarze, Matthew P. Sweet, Sara L. Zettervall	1
2	Splenic artery pathology presentation, operative interventions, and outcomes in 88 patients with vascular Ehlers-Danlos syndrome 2023 ·Journal of Vascular Surgery ·Sherene Shalhub, (unknown), (unknown), (unknown), Sandeep Vaidya, Ulrike Schwarze, Peter H. Byers	5
3	Endovascular Repair of Internal Mammary Artery Aneurysms in 2 Sisters with SMAD3 Mutation 2017 ·Annals of Vascular Surgery ·(unknown), Sherene Shalhub, Gabriel S. Aldea, Peter H. Byers, Ulrike Schwarze, Mitzi L. Murray, Benjamin W. Starnes	9
4	Altered behavioral and neural responsiveness to counterfactual gains in the elderly 2016 ·Cognitive Affective & Behavioral Neuroscience ·Michael J. Tobia, (unknown), Jan Gläscher, Ulrike Schwarze, Stefanie Brassen, Christian Büchel, Klaus Obermayer, Tobias Sommer	6
5	The challenge of comprehensive and consistent sequence variant interpretation between clinical laboratories 2015 ·Genetics in Medicine ·Melanie Pepin, Mitzi L. Murray, S.S. Bailey, (unknown), Ulrike Schwarze, Peter H. Byers	44
6	Survival is affected by mutation type and molecular mechanism in vascular Ehlers–Danlos syndrome (EDS type IV) 2014 ·Genetics in Medicine ·Melanie Pepin, Ulrike Schwarze, Kenneth Rice, (unknown), Dru F. Leistritz, Peter H. Byers	176
7	Neural systems for choice and valuation with counterfactual learning signals 2013 ·NeuroImage ·Michael J. Tobia, (unknown), Ulrike Schwarze, (unknown), Jan Gläscher, Barbara Finckh, Andreas Marschner, Christian Büchel, Klaus Obermayer, Tobias Sommer	25
8	Estrogen and the male hippocampus: Genetic variation in the aromatase gene predicting serum estrogen is associated with hippocampal gray matter volume in men 2012 ·Hippocampus ·Janine Bayer, Gabriele M. Rune, Kerstin Kutsche, Ulrike Schwarze, Raffaël Kalisch, Christian Büchel, Tobias Sommer	9
9	Homozygosity for a Missense Mutation in SERPINH1, which Encodes the Collagen Chaperone Protein HSP47, Results in Severe Recessive Osteogenesis Imperfecta 2010 ·The American Journal of Human Genetics ·Helena E. Christiansen, Ulrike Schwarze, Shawna M. Pyott, Abdulrahman Alswaid, Mohammed Al Balwi, (unknown), Melanie Pepin, Mary Ann Weis, David R. Eyre, Peter H. Byers	228
10	Molecular mechanisms of classical Ehlers-Danlos syndrome (EDS) 2009 ·Human Mutation ·Anna L. Mitchell, Ulrike Schwarze, (unknown), Peter H. Byers	33
11	Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype–phenotype relationships 2008 ·Human Molecular Genetics ·Dale L. Bodian, Ting‐Fung Chan, Annie Poon, Ulrike Schwarze, (unknown), Peter H. Byers, Pui–Yan Kwok, Teri E. Klein	85
12	MRI of great vessel morphology and function in Ehlers-Danlos syndrome type IV 2007 ·International journal of cardiac imaging ·William Kerwin, Melanie Pepin, Lee M. Mitsumori, Vasily L. Yarnykh, Ulrike Schwarze, Peter H. Byers	13
13	CRTAP Is Required for Prolyl 3- Hydroxylation and Mutations Cause Recessive Osteogenesis Imperfecta 2006 ·Cell ·Roy Morello, Terry Bertin, Yuqing Chen, John Hicks, Laura Tonachini, Massimiliano Monticone, Patrizio Castagnola, Frank Rauch, Francis H. Glorieux, Janice A. Vranka, Hans Peter Bächinger, James M. Pace, Ulrike Schwarze, Peter H. Byers, MaryAnn Weis, Russell J. Fernandes, David R. Eyre, Zhenqiang Yao, Brendan F. Boyce, Brendan Lee	366
14	Order of Intron Removal Influences Multiple Splice Outcomes, Including a Two-Exon Skip, in a COL5A1 Acceptor-Site Mutation That Results in Abnormal Pro-α1(V) N-Propeptides and Ehlers-Danlos Syndrome Type I 2002 ·The American Journal of Human Genetics ·Kazuhiko Takahara, Ulrike Schwarze, Yasutada Imamura, Guy G. Hoffman, Helga V. Toriello, Lynne T. Smith, Peter H. Byers, Daniel S. Greenspan	86
15	Clinical and Genetic Features of Ehlers–Danlos Syndrome Type IV, the Vascular Type breakdown → 2000 ·New England Journal of Medicine ·Melanie Pepin, Ulrike Schwarze, Andrea Superti‐Furga, Peter H. Byers	814
16	Redefinition of Exon 7 in the COL1A1 Gene of Type I Collagen by an Intron 8 Splice-Donor–Site Mutation in a Form of Osteogenesis Imperfecta: Influence of Intron Splice Order on Outcome of Splice-Site Mutation 1999 ·The American Journal of Human Genetics ·Ulrike Schwarze, Barbra J. Starman, Peter H. Byers	59
17	Non-radioactive multiplex-SSCP analysis: detection of a new type II procollagen gene (COL2A1) mutation 1995 ·Human Genetics ·Andreas Winterpacht, Katja Hilbert, Ulrike Schwarze, Bernhard Zabel	10
18	Autosomal dominant spondylarthropathy due to a type II procollagen gene(COL2A1) point mutation 1994 ·Human Mutation ·Andreas Winterpacht, (unknown), Ulrike Schwarze, Stefan Mundlos, J. Spranger, Bernhard Zabel	17
19	Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect 1993 ·Nature Genetics ·Andreas Winterpacht, (unknown), Ulrike Schwarze, Stefan Mundlos, J. Spranger, Bernhard Zabel	122
20	Retinoschisis mit zentral gelegenem Außenschichtriesenriß und Begleitamotio 1990 ·Klinische Monatsblätter für Augenheilkunde ·Ulrike Schwarze, H. Laqua	4

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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