Nancy D. Leslie

2.5k total citations · 1 hit paper
37 papers, 1.7k citations indexed

About

Nancy D. Leslie is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Nancy D. Leslie has authored 37 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 11 papers in Physiology. Recurrent topics in Nancy D. Leslie's work include Metabolism and Genetic Disorders (12 papers), Lysosomal Storage Disorders Research (9 papers) and Neonatal Health and Biochemistry (6 papers). Nancy D. Leslie is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Lysosomal Storage Disorders Research (9 papers) and Neonatal Health and Biochemistry (6 papers). Nancy D. Leslie collaborates with scholars based in United States, Germany and France. Nancy D. Leslie's co-authors include Jerry R. Mendell, Kandice Roush, Maha Mahmoud, Brett Duval, Cindy Hamil, Chris Shilling, Roula Al‐Dahhak, Diane M. Dunn, Robert B. Weiss and Natalie Street and has published in prestigious journals such as PEDIATRICS, Annals of Neurology and The Journal of Pediatrics.

In The Last Decade

Nancy D. Leslie

37 papers receiving 1.6k 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.

Evidence‐based path to newborn screening for duchenne muscular dystrophy

2012 607 citations Jerry R. Mendell, Chris Shilling et al. Annals of Neurology profile →

Peers

Countries citing papers authored by Nancy D. Leslie

Since Specialization

Citations

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

Fields of papers citing papers by Nancy D. Leslie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nancy D. Leslie. 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 Nancy D. Leslie. The network helps show where Nancy D. Leslie may publish in the future.

Co-authorship network of co-authors of Nancy D. Leslie

This figure shows the co-authorship network connecting the top 25 collaborators of Nancy D. Leslie. A scholar is included among the top collaborators of Nancy D. Leslie 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 Nancy D. Leslie. Nancy D. Leslie 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	Clinically available testing options resulting in diagnosis in post-exome clinic at one medical center 2022 ·Frontiers in Genetics ·Elizabeth Baker, (unknown), (unknown), (unknown), Barbara Hallinan, Nancy D. Leslie, Alexander Miethke, (unknown), Yaning Wu, Loren D.M. Peña	1
2	Motor Responses in Pediatric Pompe Disease in the ADVANCE Participant Cohort 2022 ·Journal of Neuromuscular Diseases ·Tina Duong, Priya S. Kishnani, Kristina An Haack, Meredith C. Foster, James B. Gibson, Catherine Wilson, Si Houn Hahn, Richard E. Hillman, David Kronn, Nancy D. Leslie, Loren Peña, Susan Sparks, David W. Stockton, Pranoot Tanpaiboon, John Day	3
3	Participant choices for return of genomic results in the eMERGE Network 2020 ·Genetics in Medicine ·Christin Hoell, Julia Wynn, Luke V. Rasmussen, Keith Marsolo, Sharon Aufox, Wendy K. Chung, John J. Connolly, Robert R. Freimuth, (unknown), Håkon Håkonarson, Margaret Harr, Ingrid A. Holm, Iftikhar J. Kullo, Philip E. Lammers, Kathleen A. Leppig, Nancy D. Leslie, Melanie F. Myers, Richard R. Sharp, Maureen E. Smith, Cynthia A. Prows	24
4	Clinical characteristics and genotypes in the ADVANCE baseline data set, a comprehensive cohort of US children and adolescents with Pompe disease 2019 ·Genetics in Medicine ·Priya S. Kishnani, James B. Gibson, Michael J. Gambello, Richard E. Hillman, David W. Stockton, David Kronn, Nancy D. Leslie, Loren Peña, Pranoot Tanpaiboon, John Day, Raymond Wang, Jennifer Goldstein, Kristina An Haack, Susan Sparks, Yang Zhao, Si Houn Hahn	9
5	Acquired ornithine transcarbamylase deficiency in pediatric and adolescent patients with fibrolamellar hepatocellular carcinoma 2018 ·Pediatric Blood & Cancer ·(unknown), Nancy D. Leslie, Anita Gupta, James I. Geller	8
6	Efficacy, safety profile, and immunogenicity of alglucosidase alfa produced at the 4,000-liter scale in US children and adolescents with Pompe disease: ADVANCE, a phase IV, open-label, prospective study 2018 ·Genetics in Medicine ·Si Houn Hahn, David Kronn, Nancy D. Leslie, Loren Peña, Pranoot Tanpaiboon, Michael J. Gambello, James B. Gibson, Richard E. Hillman, David W. Stockton, John Day, Raymond Wang, Kristina An Haack, Raheel Shafi, Susan Sparks, Yang Zhao, Catherine Wilson, Priya S. Kishnani	21
7	Inborn Errors of Metabolism Collaborative: large-scale collection of data on long-term follow-up for newborn-screened conditions 2016 ·Genetics in Medicine ·Susan A. Berry, Nancy D. Leslie, Mathew J. Edick, (unknown), (unknown), Cynthia A. Cameron	7
8	Mucopolysaccharidosis Type I Newborn Screening: Best Practices for Diagnosis and Management 2016 ·The Journal of Pediatrics ·L. Clarke, Andrea M. Atherton, Barbara K. Burton, Debra Day‐Salvatore, Paige Kaplan, Nancy D. Leslie, C. Ronald Scott, David W. Stockton, Janet A. Thomas, Joseph Muenzer	58
9	Outcomes of four patients with homocysteine remethylation disorders detected by newborn screening 2015 ·Genetics in Medicine ·Derek A. Wong, Silvia Tortorelli, L.A. Bishop, Elizabeth A. Sellars, Lisa A. Schimmenti, Natalie M. Gallant, Carlos E. Prada, Robert J. Hopkin, Nancy D. Leslie, Susan A. Berry, David S. Rosenblatt, (unknown), Dietrich Matern, Kimiyo Raymond, Devin Oglesbee, Piero Rinaldo, Dimitar Gavrilov	21
10	Recurrent pancreatitis in ornithine transcarbamylase deficiency 2012 ·Molecular Genetics and Metabolism ·Carlos E. Prada, Ajay Kaul, Robert J. Hopkin, (unknown), Jaimie D. Nathan, Dennis W. Bartholomew, Mitchell B. Cohen, James E. Heubi, Nancy D. Leslie, T. Burrow	3
11	Evidence‐based path to newborn screening for duchenne muscular dystrophy breakdown → 2012 ·Annals of Neurology ·Jerry R. Mendell, Chris Shilling, Nancy D. Leslie, Kevin M. Flanigan, Roula Al‐Dahhak, (unknown), (unknown), Diane M. Dunn, Brett Duval, (unknown), Cindy Hamil, Maha Mahmoud, Kandice Roush, (unknown), (unknown), (unknown), Natalie Street, (unknown), Robert B. Weiss	607
12	Malonyl Coenzyme A Decarboxylase Deficiency: Early Dietary Restriction and Time Course of Cardiomyopathy 2012 ·PEDIATRICS ·Carlos E. Prada, John L. Jefferies, Michelle A. Grenier, (unknown), (unknown), Robert L. Spicer, Jeffrey A. Towbin, Nancy D. Leslie	25
13	Intellectual disability, midface hypoplasia, facial hypotonia, and alport syndrome are associated with a deletion in Xq22.3 2010 ·American Journal of Medical Genetics Part A ·Jayson Rodriguez, (unknown), Ilaria Meloni, Sydney Ladd, Nancy D. Leslie, (unknown), Alessandra Renieri, Barbara R. DuPont, Roger E. Stevenson, Charles E. Schwartz, Anand K. Srivastava	13
14	Early Treatment With Alglucosidase Alfa Prolongs Long-Term Survival of Infants With Pompe Disease 2009 ·Pediatric Research ·Priya S. Kishnani, Deya Corzo, Nancy D. Leslie, Daniel Gruskin, Ans van der Ploeg, John Clancy, Rossella Parini, Gilles Morin, Michael Beck, Mislen Bauer, (unknown), (unknown), (unknown), Claire Morgan, Tara O’Meara, Susan Richards, Elisa Tsao, Hanna Mandel	232
15	A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24‐2q31 2008 ·Movement Disorders ·Donald L. Gilbert, Elizabeth J. Leslie, Mehdi Keddache, Nancy D. Leslie	10
16	An Updated Review of the Long-Term Neurological Effects of Galactosemia 2005 ·Pediatric Neurology ·(unknown), Nancy D. Leslie, Donald L. Gilbert	67
17	Undetectable maternal serum uE3 and postnatal abnormal sterol and steroid metabolism in Antley–Bixler syndrome 2004 ·American Journal of Medical Genetics Part A ·Deborah Cragun, (unknown), Cedric Shackleton, Richard I. Kelley, Nancy D. Leslie, Neil Mulrooney, Robert J. Hopkin	25
18	Antenatal Corticosteroids and Newborn Screening for Congenital Adrenal Hyperplasia 2001 ·Archives of Pediatrics and Adolescent Medicine ·Jennifer L. King, (unknown), Robert J. Hopkin, David R. Repaske, (unknown), Nancy D. Leslie	17
19	A Mouse Model of Galactose-1-Phosphate Uridyl Transferase Deficiency 1996 ·Biochemical and Molecular Medicine ·Nancy D. Leslie, Karen L. Yager, Pamela D. McNamara, Stanton Segal	70
20	The human galactose-1-phosphate uridyltransferase gene 1992 ·Genomics ·Nancy D. Leslie, (unknown), (unknown), (unknown), Judith L. Fridovich‐Keil, Louis J. Elsas	110

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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