Colleen A. Morris

9.7k total citations · 2 hit papers
67 papers, 5.8k citations indexed

About

Colleen A. Morris is a scholar working on Developmental Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, Colleen A. Morris has authored 67 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Developmental Neuroscience, 17 papers in Genetics and 16 papers in Molecular Biology. Recurrent topics in Colleen A. Morris's work include Williams Syndrome Research (53 papers), Congenital heart defects research (12 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Colleen A. Morris is often cited by papers focused on Williams Syndrome Research (53 papers), Congenital heart defects research (12 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Colleen A. Morris collaborates with scholars based in United States, Canada and Czechia. Colleen A. Morris's co-authors include Carolyn Β. Mervis, Mark T. Keating, Claire O. Leonard, Donald L. Atkinson, Jacquelyn Bertrand, Andreas Meyer‐Lindenberg, Karen F. Berman, A.D. Stock, Patricia Spallone and Bonnie Klein-Tasman and has published in prestigious journals such as New England Journal of Medicine, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Colleen A. Morris

66 papers receiving 5.6k 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.

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

1993 809 citations Colleen A. Morris, Patricia Spallone et al. profile →
Natural history of Williams syndrome: Physical characteristics

1988 511 citations Colleen A. Morris, Claire O. Leonard et al. The Journal of Pediatrics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Colleen A. Morris United States	40	3.7k	1.8k	1.4k	699	535	67	5.8k
Lucy R. Osborne Canada	32	1.1k 0.3×	1.3k 0.7×	931 0.7×	300 0.4×	182 0.3×	69	3.1k
Frank Greenberg United States	44	617 0.2×	3.1k 1.7×	3.8k 2.7×	675 1.0×	276 0.5×	112	7.2k
Dian Donnai United Kingdom	48	502 0.1×	3.1k 1.7×	3.0k 2.2×	343 0.5×	245 0.5×	177	7.8k
Jean M. Hébert United States	34	1.2k 0.3×	3.8k 2.1×	1.1k 0.8×	1.0k 1.4×	187 0.3×	83	5.5k
Chérif Beldjord France	30	470 0.1×	2.5k 1.4×	1.3k 0.9×	686 1.0×	266 0.5×	59	4.3k
Andrew A. Davis United States	26	1.1k 0.3×	1.6k 0.9×	206 0.1×	654 0.9×	191 0.4×	100	4.0k
Miguel Marín‐Padilla United States	39	1.3k 0.3×	2.4k 1.3×	594 0.4×	2.6k 3.8×	1.1k 2.1×	73	6.8k
David D. Eisenstat Canada	35	1.3k 0.4×	2.5k 1.4×	449 0.3×	1.3k 1.9×	228 0.4×	105	4.9k
Shaun D. Fouse United States	14	332 0.1×	2.4k 1.3×	1.0k 0.7×	311 0.4×	343 0.6×	20	3.3k
Susan Lindsay United Kingdom	37	393 0.1×	2.7k 1.5×	1.3k 0.9×	463 0.7×	253 0.5×	108	4.2k

Countries citing papers authored by Colleen A. Morris

Since Specialization

Citations

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

Fields of papers citing papers by Colleen A. Morris

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Colleen A. Morris. 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 Colleen A. Morris. The network helps show where Colleen A. Morris may publish in the future.

Co-authorship network of co-authors of Colleen A. Morris

This figure shows the co-authorship network connecting the top 25 collaborators of Colleen A. Morris. A scholar is included among the top collaborators of Colleen A. Morris 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 Colleen A. Morris. Colleen A. Morris 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

Kippenhan, J. Shane, Michael D. Gregory, Tiffany Nash, et al.. (2023). Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome. Journal of Neurodevelopmental Disorders. 15(1). 29–29. 2 indexed citations

Mervis, Carolyn Β., et al.. (2023). DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number. npj Genomic Medicine. 8(1). 25–25. 2 indexed citations

Morris, Colleen A., Stephen R. Braddock, Emily Chen, et al.. (2020). Health Care Supervision for Children With Williams Syndrome. PEDIATRICS. 145(2). 55 indexed citations

Morris, Colleen A., Carolyn Β. Mervis, Omar Abdul‐Rahman, et al.. (2015). 7q11.23 Duplication syndrome: Physical characteristics and natural history. American Journal of Medical Genetics Part A. 167(12). 2916–2935. 63 indexed citations

Mervis, Carolyn Β., Bonnie Klein-Tasman, Shelley L. Velleman, et al.. (2015). Children with 7q11.23 duplication syndrome: Psychological characteristics. American Journal of Medical Genetics Part A. 167(7). 1436–1450. 47 indexed citations

Butcher, Darci T., Rajat Singhania, Carolyn Β. Mervis, et al.. (2015). Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23. The American Journal of Human Genetics. 97(2). 216–227. 49 indexed citations

Mervis, Carolyn Β., Emily Lam, Edwin J. Young, et al.. (2012). Duplication of GTF2I Results in Separation Anxiety in Mice and Humans. The American Journal of Human Genetics. 90(6). 1064–1070. 57 indexed citations

Morris, Colleen A.. (2010). Introduction: Williams syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 154C(2). 203–208. 52 indexed citations

Muñoz, Karen E., Andreas Meyer‐Lindenberg, Ahmad R. Hariri, et al.. (2009). Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content. NeuroImage. 50(1). 340–346. 30 indexed citations

10.

Morris, Colleen A., et al.. (2006). Williams-Beuren syndrome : research, evaluation, and treatment. Johns Hopkins University Press eBooks. 64 indexed citations

11.

Morris, Colleen A., et al.. (2005). Adults with Williams syndrome. American Journal of Medical Genetics. 37(S6). 102–107. 63 indexed citations

12.

Mervis, Carolyn Β., et al.. (2004). Intellectual abilities and adaptive behavior of children and adolescents with Kabuki syndrome: A preliminary study. American Journal of Medical Genetics Part A. 132A(3). 248–255. 25 indexed citations

13.

Morris, Colleen A., Carolyn Β. Mervis, Holly H. Hobart, et al.. (2003). GTF2I hemizygosity implicated in mental retardation in Williams syndrome: Genotype–phenotype analysis of five families with deletions in the Williams syndrome region. American Journal of Medical Genetics Part A. 123A(1). 45–59. 125 indexed citations

14.

Mervis, Carolyn Β., Colleen A. Morris, Bonnie Klein-Tasman, et al.. (2003). Attentional Characteristics of Infants and Toddlers With Williams Syndrome During Triadic Interactions. Developmental Neuropsychology. 23(1-2). 243–268. 132 indexed citations

15.

Morris, Colleen A., Carolyn Β. Mervis, Byron F. Robinson, et al.. (1999). Long deletions of the Williams syndrome region on chromosome 7 result in more severe mental retardation. Genetics in Medicine. 1(2). 59–59. 3 indexed citations

16.

Goel, Niti, Thomas L. Ortel, Deeksha Bali, et al.. (1999). Familial antiphospholipid antibody syndrome: Criteria for disease and evidence for autosomal dominant inheritance. Arthritis & Rheumatism. 42(2). 318–327. 46 indexed citations

17.

Bird, Lynne M., Glenn F. Billman, Ronald V. Lacro, et al.. (1996). Sudden death in Williams syndrome: Report of ten cases. The Journal of Pediatrics. 129(6). 926–931. 126 indexed citations

18.

Tint, G. Stephen, Gerald Salen, Ashok K. Batta, et al.. (1995). Correlation of severity and outcome with plasma sterol levels in variants of the Smith-Lemli-Opitz syndrome. The Journal of Pediatrics. 127(1). 82–87. 117 indexed citations

19.

Morris, Colleen A., et al.. (1993). Supravalvular aortic stenosis cosegregates with a familial 6;7 translocation which disrupts the elastin gene. American Journal of Medical Genetics. 46(6). 737–744. 52 indexed citations

20.

Morris, Colleen A., et al.. (1988). Natural history of Williams syndrome: Physical characteristics. The Journal of Pediatrics. 113(2). 318–326. 511 indexed citations breakdown →

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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