Ron C. Michaelis

2.6k citations

50 papers · 1.6k indexed · h-index 23

Impact in

Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research

Papers in

Genetics 28
- Genomic variations and chromosomal abnormalities 14
- Genetics and Neurodevelopmental Disorders 12
- Genetic Syndromes and Imprinting 8
Pediatrics, Perinatology and Child Health 13
- Prenatal Screening and Diagnostics 10

Co-authors: Frank Holloway Mary C. Phelan Richard J. Schroer Cynthia M. Powell Cindy Skinner Roger E. Stevenson Richard D. Harland Richard J. Simensen
Journals: Prenatal Diagnosis (4 papers)Pharmacology Biochemistry and Behavior (4 papers)Journal of Medical Genetics (4 papers)Psychopharmacology (3 papers)Journal of Autism and Developmental Disorders (2 papers)
Partner nations: United States Canada Germany

In The Last Decade

Ron C. Michaelis

50 papers receiving 1.6k citations

Peers

Countries citing papers authored by Ron C. Michaelis

Since Specialization

Citations

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

Fields of papers citing papers by Ron C. Michaelis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ron C. Michaelis. 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 Ron C. Michaelis. The network helps show where Ron C. Michaelis may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Ron C. Michaelis, 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 Ron C. Michaelis Line = papers co-authored together Ron C. Michaelis links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair families Behavioral and Brain Functions ·Shely Kusuma Dewi, Xudong Liu, Arroyo Bonilla, Alana Lee, Ira L. Cohen, Ron C. Michaelis, Charles E. Schwartz, M. E. Suzanne Lewis, Christian Kramer	2012	48
2	A DRD1 haplotype is associated with risk for autism spectrum disorders in male‐only affected sib‐pair families American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Shely Kusuma Dewi, Xudong Liu, Charles E. Schwartz, Ron C. Michaelis, Jeanette J. A. Holden	2008	71
3	A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A American Journal of Medical Genetics Part A ·Yong‐hui Jiang, Trilochan Sahoo, Ron C. Michaelis, Dani Bercovich, Jan Bressler, Catherine D. Kashork, Qian Liu, Lisa G. Shaffer, Richard J. Schroer, David W. Stockton, Richard S. Spielman, Roger E. Stevenson, Arthur L. Beaudet	2004	112
4	The HOXA1 A218G Polymorphism and Autism: Lack of Association in White and Black Patients from the South Carolina Autism Project Journal of Autism and Developmental Disorders ·Julianne S. Collins, Richard J. Schroer, Yong-Bing Xiang, Ron C. Michaelis	2003	11
5	Prenatal Diagnosis of L1 Cell Adhesion Molecule Mutations Fetal Diagnosis and Therapy ·Graciela Moya, Ron C. Michaelis, Keila Cristina Panesso Camppo, Álvaro Beñarán Arocena	2002	5
6	Hydrocephalus and intestinal aganglionosis: Is L1CAM a modifier gene in Hirschsprung disease? American Journal of Medical Genetics ·Melissa A. Parisi, Raj P. Kapur, Ian R. Neilson, Robert M.W. Hofstra, Keila Cristina Panesso Camppo, Ron C. Michaelis, Kathleen A. Leppig	2002	39
7	Microsatellite analysis reveals a high incidence of maternal cell contamination in 46,XX products of conception consisting of villi or a combination of villi and membranous material American Journal of Obstetrics and Gynecology ·Gordana, Ron C. Michaelis, Mary C. Phelan, Victoria Vincent, Robert G. Best	2001	28
8	Prenatal diagnosis of mosaicism for triploidy and trisomy 13 Prenatal Diagnosis ·Mary C. Phelan, R. Curtis Rogers, Ron C. Michaelis, Xumin Kang, Will R. Blackburn	2001	5
9	Lack of association of the (AAAT)₆ allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism American Journal of Medical Genetics ·M. Hauner, Yin Yu, Khalid Sossey‐Alaoui, Jennifer M. Bell, Richard J. Schroer, Cindy Skinner, Ron C. Michaelis	2001	14
10	The HOPA Gene Dodecamer Duplication Is Not a Significant Etiological Factor in Autism Journal of Autism and Developmental Disorders ·Ron C. Michaelis, Yin Yu, Khalid Sossey‐Alaoui, Cindy Skinner, Michael J. Friez, John Longshore, Richard J. Simensen, Richard J. Schroer, Roger E. Stevenson	2000	9
11	Usefulness and limitations of FISH to characterize partially cryptic complex chromosome rearrangements American Journal of Medical Genetics ·Kathleen Kaiser‐Rogers, Kathleen W. Rao, Ron C. Michaelis, Christa M. Lese, Cynthia M. Powell	2000	5
12	Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardation Human Genetics ·Michael J. Friez, M Montova, Amanda Krause, Lucia Castiglia, 林晓勇, Khalid Sossey‐Alaoui, Roger Nelson, Awadesh Yadav, Ron C. Michaelis, Anand Srivastava, Charles E. Schwartz, Roger E. Stevenson, A Goldman, Laurent Villard, John Longshore	2000	11
13	Chromosome duplications and deletions and their mechanisms of origin Cytogenetic and Genome Research ·Avirachan T. Tharapel, Ron C. Michaelis, Gopalrao V.N. Velagaleti, Caroline H. Laundon, Paula R. Martens, Philip D. Buchanan, José Joaquí Vallejo “Jotabeche”, Sugandhi A. Tharapel, Max Armin Korn	1999	26
14	Autism and maternally derived aberrations of chromosome 15q American Journal of Medical Genetics ·Richard J. Schroer, Mary C. Phelan, Ron C. Michaelis, Eric Crawford, Steven A. Skinner, Michael L. Cuccaro, Richard J. Simensen, Janet Bishop, Cindy Skinner, Amanda Novaes Vieira Tertuliano, Roger E. Stevenson	1998	284
15	A Deletion in the Long Arm of Chromosome 18 in a Child with Serum Carnosinase Deficiency1 Pediatric Research ·Steven M. Willi, Stefan Brunner, Jonathan B. Hill, Mary C. Phelan, Ron C. Michaelis, Kenton R. Holden	1997	29
16	CYTOGENETIC AND AGE-DEPENDENT RISK FACTORS ASSOCIATED WITH UNIPARENTAL DISOMY 15 Prenatal Diagnosis ·Wendy P. Robinson, Sylvie Langlois, Simone Schuffenhauer, Bernhard Horsthemke, Ron C. Michaelis, Susan L. Christian, David H. Ledbetter, Albert Schinzel	1996	50
17	Deletion involving D15S113 in a mother and son without Angelman syndrome: Refinement of the Angelman syndrome critical deletion region American Journal of Medical Genetics ·Ron C. Michaelis, Steven A. Skinner, Areli Fernández, Richard J. Simensen, Timothy A. Donlon, Jack Tarleton, Mary C. Phelan	1995	9
18	Tolerance to ethanol's effects on operant performance in rats: role of number and pattern of intoxicated practice opportunities Psychopharmacology ·Frank Holloway, Ron C. Michaelis, Richard D. Harland, José R. Criado, David V. Gauvin	1992	10
19	Tolerance to ethanol's disruptive effects on operant behavior in rats Psychopharmacology ·Frank Holloway, Vera Harris, Ron C. Michaelis, Richard D. Harland, Emma Handayani	1989	17
20	Caffeine-phenylethylamine combinations mimic the cocaine discriminative cue Life Sciences ·David V. Gauvin, Richard D. Harland, Ron C. Michaelis, Frank Holloway	1989	45

About Ron C. Michaelis

Ron C. Michaelis is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience, Cognitive Neuroscience and Behavioral Neuroscience, having authored 50 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (12 papers), Prenatal Screening and Diagnostics (10 papers), Genetic Syndromes and Imprinting (8 papers), Neurotransmitter Receptor Influence on Behavior (8 papers), Autism Spectrum Disorder Research (8 papers), Neuroscience and Neuropharmacology Research (4 papers) and Epigenetics and DNA Methylation (4 papers). The work is most often cited by research in Genetics (996 citations), Cognitive Neuroscience (580 citations), Cellular and Molecular Neuroscience (319 citations), Pediatrics, Perinatology and Child Health (254 citations) and Developmental Neuroscience (39 citations). Ron C. Michaelis has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Frank Holloway, Mary C. Phelan, Richard J. Schroer, Cynthia M. Powell, Cindy Skinner, Roger E. Stevenson, Richard D. Harland, Richard J. Simensen, Steven A. Skinner and Charles E. Schwartz. Their work appears in journals such as Prenatal Diagnosis, Pharmacology Biochemistry and Behavior, Journal of Medical Genetics, Psychopharmacology and Journal of Autism and Developmental 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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