John B. Moeschler

6.7k total citations
62 papers, 2.6k citations indexed

About

John B. Moeschler is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, John B. Moeschler has authored 62 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Genetics, 22 papers in Molecular Biology and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in John B. Moeschler's work include Genomic variations and chromosomal abnormalities (21 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Prenatal Screening and Diagnostics (15 papers). John B. Moeschler is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Prenatal Screening and Diagnostics (15 papers). John B. Moeschler collaborates with scholars based in United States, Canada and United Kingdom. John B. Moeschler's co-authors include Michael Shevell, John M. Graham, Marilyn C. Jones, John M. Opitz, Joan M. Stoler, Rizwan Hamid, Beth A. Tarini, Emily Chen, Robert A. Saul and Debra Freedenberg and has published in prestigious journals such as Nature Genetics, Neurology and PEDIATRICS.

In The Last Decade

John B. Moeschler

61 papers receiving 2.4k citations

Peers

Countries citing papers authored by John B. Moeschler

Since Specialization

Citations

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

Fields of papers citing papers by John B. Moeschler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John B. Moeschler. 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 John B. Moeschler. The network helps show where John B. Moeschler may publish in the future.

Co-authorship network of co-authors of John B. Moeschler

This figure shows the co-authorship network connecting the top 25 collaborators of John B. Moeschler. A scholar is included among the top collaborators of John B. Moeschler 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 John B. Moeschler. John B. Moeschler 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	The metabolic evaluation of the child with an intellectual developmental disorder: Diagnostic algorithm for identification of treatable causes and new digital resource 2014 ·Molecular Genetics and Metabolism ·Clara van Karnebeek, Michael Shevell, Johannes Zschocke, John B. Moeschler, Sylvia Stöckler	93
2	Comprehensive Evaluation of the Child With Intellectual Disability or Global Developmental Delays 2014 ·PEDIATRICS ·John B. Moeschler, Michael Shevell, Robert A. Saul, Emily Chen, Debra Freedenberg, Rizwan Hamid, Marilyn C. Jones, Joan M. Stoler, Beth A. Tarini	352
3	Evidence Report: Genetic and metabolic testing on children with global developmental delay [RETIRED] 2011 ·Neurology ·David Michelson, Michael Shevell, Elliott H. Sherr, John B. Moeschler, Andrea Gropman, Stephen Ashwal	168
4	Invited comment on terminology 2011 ·American Journal of Medical Genetics Part A ·John B. Moeschler, (unknown)	4
5	FG syndrome, an X-linked multiple congenital anomaly syndrome: The clinical phenotype and an algorithm for diagnostic testing 2009 ·Genetics in Medicine ·Robin D. Clark, John M. Graham, Michael J. Friez, Joe J. Hoo, Kenneth Lyons Jones, C McKeown, John B. Moeschler, F. Lucy Raymond, R. Curtis Rogers, Charles E. Schwartz, Agatino Battaglia, Michael J. Lyons, Roger E. Stevenson	27
6	Improving genetic health care: A Northern New England pilot project addressing the genetic evaluation of the child with developmental delays or intellectual disability 2009 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·John B. Moeschler, Roberto Amato, (unknown), Leah W. Burke, Mary Beth Dinulos, Rosemarie Smith, Wendy E. Smith, Patrick Miller	13
7	Genetic Evaluation of Intellectual Disabilities 2008 ·Seminars in Pediatric Neurology ·John B. Moeschler	57
8	Medical genetics diagnostic evaluation of the child with global developmental delay or intellectual disability 2008 ·Current Opinion in Neurology ·John B. Moeschler	37
9	A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome 2007 ·Nature Genetics ·Hiba Risheg, John M. Graham, Robin D. Clark, R. Curtis Rogers, John M. Opitz, John B. Moeschler, (unknown), Melanie May, Sumy Joseph, Julie R. Jones, Roger E. Stevenson, Charles E. Schwartz, Michael J. Friez	152
10	Neuroimaging findings in macrocephaly–capillary malformation: A longitudinal study of 17 patients 2007 ·American Journal of Medical Genetics Part A ·Robert L. Conway, Barry D. Pressman, William B. Dobyns, Moise Danielpour, John Lee, Pedro A. Sanchez‐Lara, Merlin G. Butler, Elaine H. Zackai, (unknown), Sulagna C. Saitta, Carol L. Clericuzio, Jeff M. Milunsky, H. Eugene Hoyme, Joseph T.C. Shieh, John B. Moeschler, Barbara F. Crandall, Julie Lauzon, David Viskochil, Brian Harding, John M. Graham	78
11	Clinical Genetic Evaluation of the Child With Mental Retardation or Developmental Delays 2006 ·PEDIATRICS ·John B. Moeschler, Michael Shevell	166
12	Evaluation of mental retardation: Recommendations of a consensus conference 1997 ·American Journal of Medical Genetics ·Cynthia J. Curry, Roger E. Stevenson, David J. Aughton, Janice L. B. Byrne, John C. Carey, Suzanne B. Cassidy, Christopher Cunniff, John M. Graham, Marilyn C. Jones, Michael M. Kaback, John B. Moeschler, G. Bradley Schaefer, Stuart Schwartz, Jack Tarleton, John M. Opitz	266
13	Radiological features in Brachmann‐de Lange syndrome 1993 ·American Journal of Medical Genetics ·Stephen R. Braddock, Ralph S. Lachman, (unknown), John C. Carey, (unknown), John B. Moeschler, Christopher Cunniff, John M. Graham	24
14	Mild Brachmann‐de Lange syndrome. Phenotypic and developmental characteristics of mildly affected individuals 1993 ·American Journal of Medical Genetics ·John B. Moeschler, John M. Graham	16
15	Trisomy 18 and 18p‐ features in a case of isochromosome 18q [46,XY,i(18q)]: prenatal diagnosis and autopsy report 1991 ·Clinical Genetics ·Doris H. Wurster‐Hill, (unknown), John B. Moeschler, Jonathan P. Park, (unknown)	11
16	Autosomal dominant familial spastic paraplegia: report of a large New England family 1990 ·Clinical Genetics ·W. Carl Cooley, (unknown), (unknown), (unknown), Damhnat McCann, (unknown), Joseph Coughlan, John B. Moeschler	7
17	Acrocallosal syndrome: New findings 1989 ·American Journal of Medical Genetics ·John B. Moeschler, Barbara R. Pober, Lewis B. Holmes, John M. Graham	18
18	Trisomy 20 mosaicism confirmed in a phenotypically normal liveborn 1989 ·Prenatal Diagnosis ·(unknown), John B. Moeschler, (unknown), (unknown), Doris H. Wurster‐Hill	11
19	Further delineation of the 10p deletion syndrome. 1984 ·PubMed ·(unknown), John C. Carey, Gordon K. Livingston, John B. Moeschler, Mark Lubinsky	13
20	Use of the CT scan in the medical evaluation of the mentally retarded child 1981 ·The Journal of Pediatrics ·John B. Moeschler, Forrest C. Bennett, Laurence D. Cromwell	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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