Stephanie E Wallace

3.6k total citations · 1 hit paper
37 papers, 1.8k citations indexed

About

Stephanie E Wallace is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Stephanie E Wallace has authored 37 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Stephanie E Wallace's work include Connective tissue disorders research (7 papers), Aortic Disease and Treatment Approaches (5 papers) and BRCA gene mutations in cancer (3 papers). Stephanie E Wallace is often cited by papers focused on Connective tissue disorders research (7 papers), Aortic Disease and Treatment Approaches (5 papers) and BRCA gene mutations in cancer (3 papers). Stephanie E Wallace collaborates with scholars based in United States, France and United Kingdom. Stephanie E Wallace's co-authors include Michael A. Pfaller, Richard P. Wenzel, Ronald N. Jones, Donna K. McClish, Michael B. Edmond, Dušan Pavčnik, K C Wright, Dianna M. Milewicz, Ellen S. Regalado and William R. Wilcox and has published in prestigious journals such as SHILAP Revista de lepidopterología, Clinical Infectious Diseases and Radiology.

In The Last Decade

Stephanie E Wallace

35 papers receiving 1.8k 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.

Nosocomial Bloodstream Infections in United States Hospitals: A Three‐Year Analysis

1999 1.1k citations Michael B. Edmond, Stephanie E Wallace et al. Clinical Infectious Diseases profile →

Peers

Countries citing papers authored by Stephanie E Wallace

Since Specialization

Citations

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

Fields of papers citing papers by Stephanie E Wallace

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephanie E Wallace. 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 Stephanie E Wallace. The network helps show where Stephanie E Wallace may publish in the future.

Co-authorship network of co-authors of Stephanie E Wallace

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie E Wallace. A scholar is included among the top collaborators of Stephanie E Wallace 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 Stephanie E Wallace. Stephanie E Wallace 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	Evaluation of Targeted Therapies Currently Available for Congenital Genetic Conditions Indexed in GeneReviews 2025 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Nina Adam, (unknown), Stephanie E Wallace, (unknown), Ghayda Mirzaa, Margaret P Adam	2
2	Cellular senescence in acute human infectious disease: a systematic review 2024 ·SHILAP Revista de lepidopterología ·(unknown), Stephanie E Wallace, (unknown), Erin E. Reardon, Nicole Theis‐Mahon, Negar Yousefzadeh, E Schmidt, Laura J. Niedernhofer, Michael A. Puskarich	1
3	Multiplexed Biosensing of Proteins and Virions with Disposable Plasmonic Assays 2023 ·ACS Sensors ·Stephanie E Wallace, (unknown), (unknown), Christopher Davis, Agnieszka M. Szemiel, (unknown), Swetha Víjayakríshnan, Sarah Cole, Giuditta De Lorenzo, Emmanuel Maillart, (unknown), Adrian J. Lapthorn, Arvind H. Patel, Nikolaj Gadegaard, Malcolm Kadodwala, Edward Hutchinson, Affar S. Karimullah	8
4	Pre-existing Hepatic Encephalopathy: Really a Contraindication to Elective TIPS? 2023 ·CardioVascular and Interventional Radiology ·Pooya Torkian, Stephanie E Wallace, Nicholas Lim, Siobhan Flanagan, Jafar Golzarian, Shamar Young	1
5	Biocompatible, Multi-Mode, Fluorescent, T2 MRI Contrast Magnetoelectric-Silica Nanoparticles (MagSiNs), for On-Demand Doxorubicin Delivery to Metastatic Cancer Cells 2022 ·Pharmaceuticals ·(unknown), (unknown), (unknown), Stephanie E Wallace, (unknown), (unknown), (unknown), Ryan K. Roeder, Paul Helquist, M. Sharon Stack, Prakash D. Nallathamby	6
6	Genetic aortic disease epidemiology, management principles, and disparities in care 2021 ·Seminars in Vascular Surgery ·Sherene Shalhub, Stephanie E Wallace, (unknown), Karina Newhall	8
7	The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy 2019 ·Genetics in Medicine ·Amélie Pinard, Stéphanie Guey, Dongchuan Guo, Alana C. Cecchi, (unknown), Stephanie E Wallace, Ellen S. Regalado, Ellen M. Hostetler, Anjail Sharrief, Françoise Bergametti, Manoëlle Kossorotoff, Dominique Hervé, Markus Kraemer, Michael J. Bamshad, Deborah A. Nickerson, Edward R. Smith, Elisabeth Tournier‐Lasserve, Dianna M. Milewicz	34
8	Assessment of the Information Sources and Interest in Research Collaboration Among Individuals with Vascular Ehlers-Danlos Syndrome 2019 ·Annals of Vascular Surgery ·Sherene Shalhub, (unknown), (unknown), Stephanie E Wallace, (unknown), Lara Bloom, Martha Driessnack, Peter H. Byers	14
9	Resources for Genetics Professionals — Direct-to-Consumer Genetic Testing 2019 ·Stephanie E Wallace, Lora Jh Bean	0
10	MYLK pathogenic variants aortic disease presentation, pregnancy risk, and characterization of pathogenic missense variants 2018 ·Genetics in Medicine ·Stephanie E Wallace, Ellen S. Regalado, Limin Gong, (unknown), Dongchuan Guo, Claudio Russo, Richard J. Kulmacz, Nadine Hanna, Guillaume Jondeau, Cathérine Boileau, Pauline Arnaud, Kwanghyuk Lee, Suzanne M. Leal, (unknown), Bo Carlberg, (unknown), (unknown), Ellen M. Hostetler, Roberto Colombo, Dianna M. Milewicz	30
11	LTBP3 Pathogenic Variants Predispose Individuals to Thoracic Aortic Aneurysms and Dissections 2018 ·The American Journal of Human Genetics ·Dongchuan Guo, Ellen S. Regalado, Amélie Pinard, Jiyuan Chen, Kwanghyuk Lee, Christina Rigelsky, Lior Zilberberg, Ellen M. Hostetler, Micheala A. Aldred, Stephanie E Wallace, Siddharth K. Prakash, Suzanne M. Leal, Michael J. Bamshad, Deborah A. Nickerson, Marvin R. Natowicz, Daniel B. Rifkin, Dianna M. Milewicz	40
12	Impact of preoperative screening for rectal colonization with fluoroquinolone-resistant enteric bacteria on the incidence of sepsis following transrectal ultrasound guided prostate biopsy 2017 ·Research and Reports in Urology ·John Farrell, Jennifer L. Hicks, Stephanie E Wallace, Allen D. Seftel	7
13	Precision medical and surgical management for thoracic aortic aneurysms and acute aortic dissections based on the causative mutant gene. 2016 ·PubMed ·Dianna M. Milewicz, Ellen M. Hostetler, Stephanie E Wallace, (unknown), Limin Gong, Hariyadarshi Pannu, Dongchuan Guo, Ellen S. Regalado	21
14	Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome 2016 ·Molecular Case Studies ·Linda M. Polfus, Eric Boerwinkle, Richard A. Gibbs, Ginger Metcalf, Donna M. Muzny, Narayanan Veeraraghavan, Megan L. Grove, Sanjay Shete, Stephanie E Wallace, Dianna M. Milewicz, Neil A. Hanchard, James R. Lupski, S. Shahrukh Hashmi, Monesha Gupta‐Malhotra	9
15	A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations 2014 ·Neuromuscular Disorders ·Stephanie E Wallace, Jessie H. Conta, Thomas Winder, Tobias Willer, (unknown), Richard Haas, Kathleen Patterson, Kevin P. Campbell, Steven A. Moore, Sídney M. Gospe	12
16	Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity 2010 ·Genetics in Medicine ·Ruxandra Bachmann‐Gagescu, Heather C. Mefford, Charles A. Cowan, Gwen M. Glew, Anne Hing, Stephanie E Wallace, Patricia I. Bader, (unknown), Pamela J. Reitnauer, Rosemarie Smith, David W. Stockton, Hiltrud Muhle, Ingo Helbig, Evan E. Eichler, Blake C. Ballif, Jill A. Rosenfeld, Karen D. Tsuchiya	137
17	Marked phenotypic variability in progressive diaphyseal dysplasia (Camurati–Engelmann disease): Report of a four‐generation pedigree, identification of a mutation in TGFB1, and review 2004 ·American Journal of Medical Genetics Part A ·Stephanie E Wallace, Ralph S. Lachman, Pertchoui B. Mekikian, (unknown), William R. Wilcox	44
18	Nosocomial Bloodstream Infections in United States Hospitals: A Three‐Year Analysis breakdown → 1999 ·Clinical Infectious Diseases ·Michael B. Edmond, Stephanie E Wallace, Donna K. McClish, Michael A. Pfaller, Ronald N. Jones, Richard P. Wenzel	1123
19	Development and initial experimental evaluation of a prosthetic aortic valve for transcatheter placement. Work in progress. 1992 ·Radiology ·Dušan Pavčnik, K C Wright, Stephanie E Wallace	54
20	Referrals by traditional birth attendants in northeast Brazil. 1985 ·American Journal of Public Health ·(unknown), Stephanie E Wallace, (unknown), (unknown)	24

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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