Stefanie Uhrich

1.1k total citations
21 papers, 736 citations indexed

About

Stefanie Uhrich is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Infectious Diseases. According to data from OpenAlex, Stefanie Uhrich has authored 21 papers receiving a total of 736 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Pediatrics, Perinatology and Child Health, 9 papers in Genetics and 4 papers in Infectious Diseases. Recurrent topics in Stefanie Uhrich's work include Prenatal Screening and Diagnostics (15 papers), Fetal and Pediatric Neurological Disorders (7 papers) and BRCA gene mutations in cancer (5 papers). Stefanie Uhrich is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Fetal and Pediatric Neurological Disorders (7 papers) and BRCA gene mutations in cancer (5 papers). Stefanie Uhrich collaborates with scholars based in United States, Australia and Canada. Stefanie Uhrich's co-authors include Robin L. Bennett, Kathryn A. Steinhaus, Robert G. Resta, Victoria Vincent, Dorene S. Markel, Thomas C. Winter, Kwang‐Ting Cheng, David A. Nyberg, Vivienne Souter and Debra Lochner Doyle and has published in prestigious journals such as Radiology, The American Journal of Human Genetics and American Journal of Roentgenology.

In The Last Decade

Stefanie Uhrich

20 papers receiving 700 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefanie Uhrich United States 15 331 305 120 85 78 21 736
Hanna Dar Israel 17 275 0.8× 269 0.9× 261 2.2× 82 1.0× 88 1.1× 53 796
Michal Berkenstadt Israel 15 339 1.0× 450 1.5× 204 1.7× 72 0.8× 108 1.4× 54 869
Robert Roger Lebel United States 16 174 0.5× 287 0.9× 276 2.3× 75 0.9× 116 1.5× 45 800
Kenneth L. Garver United States 11 225 0.7× 260 0.9× 160 1.3× 88 1.0× 187 2.4× 24 712
M. G. J. Jahoda Netherlands 15 648 2.0× 283 0.9× 238 2.0× 183 2.2× 149 1.9× 40 1.0k
Christine M. Armour Canada 20 358 1.1× 435 1.4× 340 2.8× 86 1.0× 73 0.9× 52 923
R. H. Lindenbaum United Kingdom 14 428 1.3× 175 0.6× 116 1.0× 64 0.8× 178 2.3× 20 760
Merel C. van Maarle Netherlands 16 309 0.9× 199 0.7× 135 1.1× 140 1.6× 105 1.3× 29 788
E.J.T. Winsor Canada 20 596 1.8× 450 1.5× 283 2.4× 107 1.3× 242 3.1× 46 1.2k
Charles M. Strom United States 16 132 0.4× 357 1.2× 241 2.0× 44 0.5× 40 0.5× 37 883

Countries citing papers authored by Stefanie Uhrich

Since Specialization
Citations

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

Fields of papers citing papers by Stefanie Uhrich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefanie Uhrich

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

All Works

20 of 20 papers shown
1.
Underhill, Hunter R., et al.. (2015). Detecting the effects of Fabry disease in the adult human brain with diffusion tensor imaging and fast bound‐pool fraction imaging. Journal of Magnetic Resonance Imaging. 42(6). 1611–1622. 6 indexed citations
2.
Fall, B., Stefanie Uhrich, Michael Mauer, et al.. (2013). Podocyturia correlates with proteinuria in patients with Fabry disease (FD) and is a potential biomarker of Fabry nephropathy. Molecular Genetics and Metabolism. 108(2). S76–S77. 2 indexed citations
3.
Uhrich, Stefanie, et al.. (2012). Four Mutations in the SI Gene Are Responsible for the Majority of Clinical Symptoms of CSID. Journal of Pediatric Gastroenterology and Nutrition. 55(S2). S34–5. 33 indexed citations
4.
Tran, Lan, Darcy B. Carr, Lee M. Mitsumori, Stefanie Uhrich, & Laurence E. Shields. (2005). Second-Trimester Biparietal Diameter/Nasal Bone Length Ratio Is an Independent Predictor of Trisomy 21. Journal of Ultrasound in Medicine. 24(6). 805–810. 15 indexed citations
5.
Bennett, Robin L., Arno G. Motulsky, A.H. Bittles, et al.. (2002). Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors. Australasian Journal of Paramedicine. 11(2). 97–119. 138 indexed citations
6.
Winter, Thomas C., et al.. (2000). Echogenic Intracardiac Focus in 2nd-Trimester Fetuses with Trisomy 21: Usefulness as a US Marker. Radiology. 216(2). 450–456. 45 indexed citations
7.
Winter, Thomas C., Stefanie Uhrich, Vivienne Souter, & David A. Nyberg. (2000). The “Genetic Sonogram”: Comparison of the Index Scoring System with the Age-adjusted US Risk Assessment. Radiology. 215(3). 775–782. 39 indexed citations
8.
Winter, Thomas C., et al.. (2000). Cerebellar and Frontal Lobe Hypoplasia in Fetuses with Trisomy 21: Usefulness as Combined US Markers. Radiology. 214(2). 533–538. 42 indexed citations
9.
Winter, Thomas C., et al.. (1998). Frontal lobe shortening in second-trimester fetuses with trisomy 21: usefulness as a US marker.. Radiology. 207(1). 215–222. 17 indexed citations
10.
Shields, Laurence E., et al.. (1996). Amniotic fluid alpha-fetoprotein determination at the time of genetic amniocentesis: has it outlived its usefulness?. Journal of Ultrasound in Medicine. 15(11). 735–739. 5 indexed citations
11.
Shields, Laurence E., Stefanie Uhrich, Thomas R. Easterling, D R Cyr, & L A Mack. (1996). Isolated fetal choroid plexus cysts and karyotype analysis: is it necessary?. Journal of Ultrasound in Medicine. 15(5). 389–394. 18 indexed citations
12.
Bennett, Robin L., Kathryn A. Steinhaus, Stefanie Uhrich, et al.. (1995). Reply to Marazita and Curtis.. The American Journal of Human Genetics. 57(4). 983–984.
13.
Steinhaus, Kathryn A., Robin L. Bennett, Robert G. Resta, et al.. (1995). Inconsistencies in pedigree symbols in human genetics publications: A need for standardization. American Journal of Medical Genetics. 56(3). 291–295. 6 indexed citations
14.
Bennett, Robin L., Kathryn A. Steinhaus, Stefanie Uhrich, et al.. (1995). Recommendations for standardized human pedigree nomenclature. Pedigree Standardization Task Force of the National Society of Genetic Counselors.. PubMed. 56(3). 745–52. 126 indexed citations
15.
Bennett, Robin L., Kathryn A. Steinhaus, Stefanie Uhrich, et al.. (1995). Recommendations for standardized human pedigree nomenclature. Journal of Genetic Counseling. 4(4). 267–279. 118 indexed citations
16.
Uhrich, Stefanie, et al.. (1994). Fetal t(5p;21q) misdiagnosed as monosomy 21: A plea for in situ hybridization studies. American Journal of Medical Genetics. 52(4). 416–418. 15 indexed citations
17.
Bennett, Robin L., et al.. (1993). The need for developing standardized family pedigree nomenclature. Journal of Genetic Counseling. 2(4). 261–273. 16 indexed citations
18.
Hendricks, Susan K., et al.. (1991). Diagnosis of polyhydramnios in early gestation: Indication for prenatal diagnosis?. Prenatal Diagnosis. 11(8). 649–654. 12 indexed citations
19.
Uhrich, Stefanie, Jack Fitzsimmons, Thomas R. Easterling, Laurence A. Mack, & Christine M. Distèche. (1991). Duplication (6q) syndrome diagnosed in utero. American Journal of Medical Genetics. 41(3). 282–283. 14 indexed citations
20.
Mack, L A, et al.. (1989). Sonography of placental abnormalities and oligohydramnios in women with elevated alpha-fetoprotein levels: comparison with control subjects. American Journal of Roentgenology. 153(4). 815–819. 29 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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