Edward J. Lose

2.8k total citations · 1 hit paper
17 papers, 1.4k citations indexed

About

Edward J. Lose is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Edward J. Lose has authored 17 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 7 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Edward J. Lose's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (7 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Edward J. Lose is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (7 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Edward J. Lose collaborates with scholars based in United States, Australia and Mexico. Edward J. Lose's co-authors include Merton Bernfield, Jürg Spring, Masato Kato, Richard L. Gallo, Robert Kokenyesi, Michael T. Hinkes, Nathaniel H. Robin, Andrew J. Carroll, Fady M. Mikhail and Bruce R. Korf and has published in prestigious journals such as Genomics, Human Genetics and Genetics in Medicine.

In The Last Decade

Edward J. Lose

17 papers receiving 1.4k 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.

Biology of the Syndecans: A Family of Transmembrane Heparan Sulfate Proteoglycans

1992 923 citations Merton Bernfield, Robert Kokenyesi et al. PubMed profile →

Peers

Countries citing papers authored by Edward J. Lose

Since Specialization

Citations

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

Fields of papers citing papers by Edward J. Lose

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edward J. Lose. 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 Edward J. Lose. The network helps show where Edward J. Lose may publish in the future.

Co-authorship network of co-authors of Edward J. Lose

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child’s Best Possible Life 2021 ·AJOB Empirical Bioethics ·Janet E. Childerhose, Carla A. Rich, Kelly M. East, Whitley V. Kelley, Shirley Simmons, Candice R. Finnila, Kevin M. Bowling, Michelle D. Amaral, Susan M. Hiatt, Michelle L. Thompson, Stacy W. Gray, James M.J. Lawlor, R Myers, Gregory S. Barsh, Edward J. Lose, (unknown), Gregory M. Cooper, Kyle B. Brothers	19
2	Menkes disease complicated by concurrent Koolen‐de Vries syndrome (17q21.31 deletion) 2019 ·Molecular Genetics & Genomic Medicine ·(unknown), (unknown), Joseph B. Philips, Edward J. Lose, Fady M. Mikhail, Anna Hurst	2
3	Genomic sequencing identifies secondary findings in a cohort of parent study participants 2018 ·Genetics in Medicine ·Michelle L. Thompson, Candice R. Finnila, Kevin M. Bowling, Kyle B. Brothers, Matthew B. Neu, Michelle D. Amaral, Susan M. Hiatt, Kelly M. East, Stacy W. Gray, James M.J. Lawlor, Whitley V. Kelley, Edward J. Lose, Carla A. Rich, Shirley Simmons, Shawn Levy, R Myers, Gregory S. Barsh, E. Martina Bebin, Gregory M. Cooper	19
4	A case report of chromosome 17q22‐qter trisomy with distinct clinical presentation and review of the literature 2018 ·Clinical Case Reports ·(unknown), Joseph B. Philips, Nathaniel H. Robin, Edward J. Lose, Fady M. Mikhail	7
5	Schaaf‐Yang syndrome overview: Report of 78 individuals 2018 ·American Journal of Medical Genetics Part A ·John McCarthy, Philip J. Lupo, (unknown), (unknown), Bret L. Bostwick, Daryl A. Scott, Katerina Kraft, Tony Roscioli, Joel Charrow, Samantha A. Schrier Vergano, Edward J. Lose, (unknown), Yves Lacassie, Christian P. Schaaf	64
6	Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results 2016 ·Genetics in Medicine ·Kyle B. Brothers, Kelly M. East, Whitley V. Kelley, (unknown), (unknown), Carla A. Rich, Kevin M. Bowling, Edward J. Lose, E. Martina Bebin, Shirley Simmons, John Myers, Gregory S. Barsh, R Myers, Gregory M. Cooper, Jill M. Pulley, Mark A. Rothstein, Ellen Wright Clayton	29
7	Clinical relevance of small copy-number variants in chromosomal microarray clinical testing 2016 ·Genetics in Medicine ·(unknown), (unknown), (unknown), Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, (unknown)	19
8	Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States 2015 ·Molecular Genetics and Metabolism ·Marcus J. Miller, Lindsay C. Burrage, James B. Gibson, (unknown), Edward J. Lose, David Bick, Sarah H. Elsea, V. Reid Sutton, Qin Sun, Brett H. Graham, William J. Craigen, Victor Wei Zhang, Lee-Jun Wong	53
9	Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders 2011 ·American Journal of Medical Genetics Part A ·Fady M. Mikhail, Edward J. Lose, Nathaniel H. Robin, Maria Descartes, (unknown), S. Lane Rutledge, Bruce R. Korf, Andrew J. Carroll	129
10	BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome 2011 ·Human Genetics ·Linda M. Reis, Rebecca C. Tyler, Kala F. Schilter, Omar Abdul‐Rahman, Jeffrey W. Innis, Beth A. Kozel, Adele Schneider, Tanya Bardakjian, Edward J. Lose, Donna M. Martin, Ulrich Broeckel, Elena V. Semina	87
11	Molecular cytogenetic characterization of two cases with constitutional distal 11q duplication/triplication 2009 ·American Journal of Medical Genetics Part A ·Rachel D. Burnside, Edward J. Lose, (unknown), José Sánchez‐Corona, Horacio Rivera, Andrew J. Carroll, Fady M. Mikhail	29
12	AsktheGeneticistSM: five years of online experience 2009 ·Genetics in Medicine ·(unknown), Bruce R. Korf, Lynn Holt, Sandra K. Prucka, Nathaniel H. Robin, Maria Descartes, Edward J. Lose, Adrya Stembridge, Michael P. Epstein, Stephen T. Warren	2
13	The emerging role of primary care in genetics 2008 ·Current Opinion in Pediatrics ·Edward J. Lose	7
14	The use by Alabama pediatricians of genetics consultation in the evaluation of developmental delay 2008 ·American Journal of Medical Genetics Part A ·(unknown), Cheryl L. Holt, Edward J. Lose, Nathaniel H. Robin	8
15	Advances in Genetic Testing and Applications in Newborn Medicine 2008 ·NeoReviews ·(unknown), Margaret Chen, Edward J. Lose, Fady M. Mikhail, Bruce R. Korf	1
16	Biology of the Syndecans: A Family of Transmembrane Heparan Sulfate Proteoglycans breakdown → 1992 ·PubMed ·Merton Bernfield, Robert Kokenyesi, Masato Kato, Michael T. Hinkes, Jürg Spring, Richard L. Gallo, Edward J. Lose	923
17	Chromosome mapping of the murine syndecan gene 1991 ·Genomics ·(unknown), Heather B. Streeter, Edward J. Lose, N G Copeland, Debra J. Gilbert, Monica J. Justice, Nancy A. Jenkins, T. Mohandas, Merton Bernfield	14

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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