Lawrence Charnas

4.4k citations

54 papers · 2.7k indexed · h-index 27

Impact in

Genetics top 2%
- Vascular Anomalies and Treatments
- Craniofacial Disorders and Treatments
Clinical Biochemistry top 2%

Papers in

Clinical Biochemistry 6
- Metabolism and Genetic Disorders 6
Biochemistry 6
- Amino Acid Enzymes and Metabolism 5

Co-authors: Paul J. Orchard Elsa Shapiro William A. Gahl Joan C. Marini Jakub Tolar Gregory F. Meyers Jen-i Mao Ethylin Wang Jabs
Journals: Molecular Genetics and Metabolism (6 papers)Bone Marrow Transplantation (5 papers)The Journal of Pediatrics (3 papers)Neurology (3 papers)Neuromuscular Disorders (2 papers)
Partner nations: United States Canada Cameroon

In The Last Decade

Lawrence Charnas

54 papers receiving 2.7k citations

Peers

Countries citing papers authored by Lawrence Charnas

Since Specialization

Citations

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

Fields of papers citing papers by Lawrence Charnas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Lawrence Charnas, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Lawrence Charnas Line = papers co-authored together Lawrence Charnas links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Dual-energy X-ray absorptiometry measures of lean body mass as a biomarker for progression in boys with Duchenne muscular dystrophy Scientific Reports ·Sarah P. Sherlock, Jeffrey Palmer, Kathryn R. Wagner, Hoda Abdel‐Hamid, Cuixia Tian, Jean K. Mah, Francesco Muntoni, Michela Guglieri, Russell J. Butterfield, Lawrence Charnas, Shannon Marraffino	2022	8
2	X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism Molecular Genetics and Metabolism ·Ying Wang, 毛毛, Catherine Reeves, Lena Bezman, Gerald V. Raymond, Anthony Litke, Paul A. Watkins, Ann Snowden, Ann B. Moser, Sakkubai Naidu, Genila Bibat, Jaclyn McKeowan, Karen Tam, Joe T.R. Clarke, Lawrence Charnas, Gail Stetten, Barbara Karczeski, Garry R. Cutting, Steven J. Steinberg	2011	32
3	Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum Nature Genetics ·Juliane Najm, Denise Horn, Isabella Wimplinger, Jeffrey A. Golden, Victor V. Chizhikov, Jyotsna Sudi, Susan L. Christian, Reinhard Ullmann, Alma Kuechler, Carola A. Haas, Mohammad Ahsan Uddin, Lawrence Charnas, Gökhan Uyanık, Ainur Kerimkulovna Kenebayeva, Eva Klopocki, William B. Dobyns, Kerstin Kutsche	2008	202
4	Combination of enzyme replacement and hematopoietic stem cell transplantation as therapy for Hurler syndrome Bone Marrow Transplantation ·Jakub Tolar, Sunping Qu, Kendra Bjoraker, C B Whitley, Elsa Shapiro, Lawrence Charnas, Paul J. Orchard	2007	99
5	Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities The American Journal of Human Genetics ·Jorune Balciuniene, Ningping Feng, Choong-Hwan Song, Betsy Hirsch, Lawrence Charnas, Brent Bill, Mathew C. Easterday, Johan Staaf, 章子大井, И. Соколов, Dimitri Avramopoulos, George H. Thomas, Åke Borg, David Valle‐García, Lisa A. Schimmenti, Scott B. Selleck	2007	85
6	Progressive brainstem compression in an infant with neurocutaneous melanosis and Dandy–Walker complex following ventriculoperitoneal shunt placement for hydrocephalus Journal of Neurosurgery Pediatrics ·Shearwood McClelland, Lawrence Charnas, Karen S. SantaCruz, Duan N. McLellan, Cornelius H. Lam	2007	19
7	Hematopoietic Cell Therapy for Metabolic Disease The Journal of Pediatrics ·Paul J. Orchard, Bruce R. Blazar, John E. Wagner, Lawrence Charnas, William Krivit, Jakub Tolar	2007	68
8	Effective treatment of α-mannosidosis by allogeneic hematopoietic stem cell transplantation The Journal of Pediatrics ·Satkiran S. Grewal, Elsa Shapiro, William Krivit, Lawrence Charnas, Lawrence A. Lockman, Kathleen Delaney, Stella M. Davies, David A. Wenger, Frank L. Rimell, Susan L. Abel, Alfred Grovas, Paul J. Orchard, John E. Wagner, Charles Peters	2004	42
9	Continued neurocognitive development and prevention of cardiopulmonary complications after successful BMT for I-cell disease: a long-term follow-up report Bone Marrow Transplantation ·Sunping Qu, Elsa Shapiro, Elizabeth Braunlin, Lawrence Charnas, William Krivit, Paul J. Orchard, Christina Peters	2003	29
10	Late occurrence of chronic immune-mediated axonal polyneuropathy following bone marrow transplant for juvenile-onset α-mannosidosis Bone Marrow Transplantation ·Daniel A. Mulrooney, Stella M. Davies, David Walk, Lawrence Charnas	2003	4
11	Linkage Studies in Erythrokeratodermias: Fine Mapping, Genetic Heterogeneity, and Analysis of Candidate Genes Journal of Investigative Dermatology ·Gabriela Richard, Jing‐Ping Lin, Lisa V. Smith, Jogi Manisha, Peter Itin, Uwe Wollina, Ervin H. Epstein, Daniel Hohl, Silva Alencar De Menezes, Lawrence Charnas, Sherri J. Bale, John J. DiGiovanna	1997	44
12	Evidence for a discrete behavioral phenotype in the oculocerebrorenal syndrome of lowe American Journal of Medical Genetics ·Lauren Kenworthy, Lawrence Charnas	1995	26
13	Neurologic Profile in Osteogenesis lmperfecta Connective Tissue Research ·Lawrence Charnas, Joan C. Marini	1995	7
14	Distal vacuolar myopathy in nephropathic cystinosis Annals of Neurology ·Lawrence Charnas, Carlos A. Luciano, Marinos C. Dalakas, R. W. Gilliatt, Isa Bernardini, Kamal G. Ishak, Valerie Cwik, Douglas L. Fraker, Dave Freund, William A. Gahl	1994	66
15	Localization of the 75-kDa inositol polyphosphate-5-phosphatase (INPP5B) to human chromosome band 1p34 Cytogenetic and Genome Research ·Pasi A. Jänne, C T Perez, Nicholas C. Dracopoli, Lawrence Charnas, Jennifer M. Puck, F. Furumoto	1994	5
16	Cognitive and behavioral profile of the oculocerebrorenal syndrome of Lowe American Journal of Medical Genetics ·Lauren Kenworthy, Taesung Park, Lawrence Charnas	1993	35
17	Nonsense mutations in the OCRL-1 gene in patients with the oculocerebrorenal syndrome of Lowe Human Molecular Genetics ·Ummah Tafsirun, Lawrence Charnas, Robert L. Nussbaum	1993	59
18	Myalgia and elevated creatine kinase activity associated with subcutaneous injections of diluent The Journal of Pediatrics ·Mark A. Bach, Denise Blum, Susan R. Rose, Lawrence Charnas	1992	11
19	The Oculocerebrorenal Syndrome of Lowe Advances in Pediatrics ·Lawrence Charnas, William A. Gahl	1991	18
20	Pulmonary arteriovenous malformations: techniques and long-term outcome of embolotherapy. Radiology ·Robert I. White, Cesar Hernandez Rosete, P. B. Terry, Philip Buescher, PourAli Reza, Lawrence Charnas, MIHARU MAEDA, Mchugh Peter, Seongmin Kang, S E Mitchell	1988	347

About Lawrence Charnas

Lawrence Charnas is a scholar working on Clinical Biochemistry, Biochemistry, Pathology and Forensic Medicine, Cell Biology and Physiology, having authored 54 papers that have together received 2.7k indexed citations. Recurring topics across this work include Biomedical Research and Pathophysiology (10 papers), Muscle Physiology and Disorders (7 papers), Metabolism and Genetic Disorders (6 papers), Lysosomal Storage Disorders Research (6 papers), Amino Acid Enzymes and Metabolism (5 papers), Peroxisome Proliferator-Activated Receptors (5 papers), Cellular transport and secretion (5 papers) and Neonatal Health and Biochemistry (3 papers). The work is most often cited by research in Genetics (463 citations), Clinical Biochemistry (211 citations), Biochemistry (211 citations), Genetics (724 citations) and Pathology and Forensic Medicine (378 citations). Lawrence Charnas has collaborated with scholars based in United States, Canada and Cameroon. Frequent co-authors include Paul J. Orchard, Elsa Shapiro, William A. Gahl, Joan C. Marini, Jakub Tolar, Gregory F. Meyers, Jen-i Mao, Ethylin Wang Jabs, Michael Jaye and Xiang Li. Their work appears in journals such as Molecular Genetics and Metabolism, Bone Marrow Transplantation, The Journal of Pediatrics, Neurology and Neuromuscular Disorders.

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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