Michael J. Lyons

2.8k citations

41 papers · 737 indexed · h-index 16

Co-authors: Kenton R. Holden Robert J. Hopkin Tracy L. Trotter Joan M. Stoler Angela E. Scheuerle Susan A. Berry Emily Chen Timothy A. Geleske
Topics: Genomic variations and chromosomal abnormalities (11 papers)Genetics and Neurodevelopmental Disorders (8 papers)Genomics and Rare Diseases (4 papers)
Cited by: Developmental Neuroscience Genetics Neurology
Journals: PEDIATRICS Human Molecular Genetics Journal of Neurology Neurosurgery & Psychiatry
Partner nations: United States Italy Canada

In The Last Decade

Michael J. Lyons

37 papers receiving 697 citations

Peers

Countries citing papers authored by Michael J. Lyons

Since Specialization

Citations

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

Fields of papers citing papers by Michael J. Lyons

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael J. Lyons

This figure shows the co-authorship network connecting the top 25 collaborators of Michael J. Lyons. A scholar is included among the top collaborators of Michael J. Lyons 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 Michael J. Lyons. Michael J. Lyons 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	Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data 2025 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Mary K. Young,(unknown),Margaret Brand,(unknown),K. Young,(unknown),Michael J. Lyons	0
2	P169 Childhood onset amyotrophic lateral sclerosis associated with SPTLC2 gain-of-function pathogenic variants: clinical, genetic, and biochemical insights 2023 ·Neuromuscular Disorders ·(unknown),(unknown),Payam Mohassel,Maike F. Dohrn,Museer A. Lone,Sandra Donkervoort,A. Reghan Foley,Danique Beijer,(unknown),Piraye Oflazer,Pinki Munot,Alison Rose,Michael J. Lyons,Francesco Muntoni,Aleksandra Ewa Basak,Teresa Dunn,(unknown),(unknown),Carsten G. Bönnemann	0
3	Recurrentde-novo gain-of-functionmutation inSPTLC2confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis 2023 ·Journal of Neurology Neurosurgery & Psychiatry ·Maike F. Dohrn,Danique Beijer,Museer A. Lone,(unknown),Piraye Oflazer,(unknown),Sandra Donkervoort,A. Reghan Foley,(unknown),Michael J. Lyons,Raymond J. Louie,Kenneth Gable,Teresa Dunn,Sitong Chen,Matt C. Danzi,Matthis Synofzik,Carsten G. Bönnemann,A. Nazlı Başak,Thorsten Hornemann,Stephan Züchner	6
4	A SOX3 duplication and lumbosacral spina bifida in three generations 2022 ·American Journal of Medical Genetics Part A ·Kameryn M. Butler,Timothy Fee,Barbara R. DuPont,Jane H. Dean,Roger E. Stevenson,Michael J. Lyons	5
5	Health Care Supervision for Children With Williams Syndrome 2020 ·PEDIATRICS ·Colleen A. Morris,Stephen R. Braddock,Emily Chen,Tracy L. Trotter,Susan A. Berry,(unknown),Timothy A. Geleske,Rizwan Hamid,Robert J. Hopkin,Wendy J. Introne,Michael J. Lyons,Angela E. Scheuerle,Joan M. Stoler	55
6	Health Supervision for People With Achondroplasia 2020 ·PEDIATRICS ·Julie Hoover‐Fong,Charles I. Scott,Marilyn C. Jones,Emily Chen,Tracy L. Trotter,Susan A. Berry,(unknown),Timothy A. Geleske,Rizwan Hamid,Robert J. Hopkin,Wendy J. Introne,Michael J. Lyons,Angela E. Scheuerle,Joan M. Stoler	70
7	Health Supervision for Children With Neurofibromatosis Type 1 2019 ·PEDIATRICS ·David T. Miller,Debra Freedenberg,Elizabeth K. Schorry,Nicole J. Ullrich,David Viskochil,Bruce R. Korf,Emily Chen,Tracy L. Trotter,Susan A. Berry,Leah W. Burke,Timothy A. Geleske,Rizwan Hamid,Robert J. Hopkin,Wendy J. Introne,Michael J. Lyons,Angela E. Scheuerle,Joan M. Stoler	117
8	Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities 2019 ·European Journal of Human Genetics ·Renee Bend,Lior Cohen,Melissa T. Carter,Michael J. Lyons,Dmitriy Niyazov,Mohamad A. Mikati,(unknown),Richard Person,Yue Si,Ingrid M. Wentzensen,Erin Torti,Jennifer A. Lee,Kym M. Boycott,Lina Basel‐Vanagaite,Carlos R. Ferreira,Claudia Gonzaga‐Jauregui	18
9	A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features 2016 ·American Journal of Medical Genetics Part A ·J. A. Smith,Kenton R. Holden,Michael J. Friez,Julie R. Jones,Michael J. Lyons	11
10	Beyond Ohdo syndrome: A familial missense mutation broadens the MED12 spectrum 2015 ·American Journal of Medical Genetics Part A ·Katherine G. Langley,(unknown),(unknown),Janelle Fox,Michael J. Friez,Michael J. Lyons,Samantha A. Schrier Vergano	14
11	Clinical utility of chromosomal microarray analysis in the diagnosis and management of monosomy 7 mosaicism 2014 ·Molecular Cytogenetics ·Alka Dwivedi,Michael J. Lyons,(unknown),Frank Bartel,Michael J. Friez,Kenton R. Holden,Eric T. Fung,Barbara R. DuPont	1
12	Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome 2014 ·American Journal of Medical Genetics Part A ·(unknown),Kenton R. Holden,Sara Cathey,Alka Dwivedi,Barbara R. DuPont,Michael J. Lyons	24
13	Chromosome 22q11.2 deletion syndrome in African‐American patients: A diagnostic challenge 2011 ·American Journal of Medical Genetics Part A ·Aravindhan Veerapandiyan,Omar Abdul‐Rahman,Margaret P Adam,Michael J. Lyons,Melanie Manning,Karlene Coleman,Lisa Kobrynski,(unknown),Kelly Schoch,Holly H. Zimmerman,Vandana Shashi	18
14	Autism in two females with duplications involving Xp11.22-p11.23 2011 ·Developmental Medicine & Child Neurology ·(unknown),Michael J. Lyons,Reyna M. Durón,Barbara R. DuPont,Kenton R. Holden	17
15	Two percent of patients suspected of having Angelman syndrome have TCF4 mutations 2010 ·Clinical Genetics ·Kyoko Takano,Michael J. Lyons,C. D. Moyes,Julie R. Jones,CE Schwartz	40
16	Novel CLCN1 Mutation in Carbamazepine-Responsive Myotonia Congenita 2010 ·Pediatric Neurology ·Michael J. Lyons,Reyna M. Durón,(unknown),Federica Sangiuolo,Kenton R. Holden	13
17	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
18	Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome 2008 ·Journal of Medical Genetics ·Michael J. Lyons,John M. Graham,Giovanni Neri,Alasdair G. W. Hunter,Robin D. Clark,R. Curtis Rogers,(unknown),Luigi Boccuto,Richard J. Simensen,Jonathan D. Dodd,(unknown),Barbara R. DuPont,Michael J. Friez,Charles E. Schwartz,Roger E. Stevenson	18
19	Early onset alpha‐mannosidosis with slow progression in three Hispanic males 2007 ·Developmental Medicine & Child Neurology ·Michael J. Lyons,Tim Wood,(unknown),Hilde Monica Frostad Riise Stensland,Kenton R. Holden	7
20	Terminal deletion of 6p results in a recognizable phenotype 2005 ·American Journal of Medical Genetics Part A ·(unknown),Athena M. Cherry,(unknown),Michael J. Lyons,H. Eugene Hoyme,Louanne Hudgins	44

About Michael J. Lyons

Michael J. Lyons is a scholar working on Genetics, Architecture and Developmental Biology, having authored 41 papers that have together received 737 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Developmental Neuroscience (49 citations), Genetics (302 citations) and Neurology (115 citations). Michael J. Lyons has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Kenton R. Holden, Robert J. Hopkin, Tracy L. Trotter, Joan M. Stoler, Angela E. Scheuerle, Susan A. Berry, Emily Chen, Timothy A. Geleske, Wendy J. Introne and Rizwan Hamid. Their work appears in journals such as PEDIATRICS, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

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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