Karlene Coleman

1.8k citations

19 papers · 873 indexed · h-index 13

Molecular Biology
Epidemiology top 10%
Genetics top 10%
Pulmonary and Respiratory Medicine top 10%
Surgery

Co-authors: William T. Mahle Robert M. Campbell Paul M. Fernhoff Kristin M. May Robert Merritt Lorenzo D. Botto Leslie A. O’Leary E. Marsha Elixson
Topics: Congenital heart defects research (12 papers)Congenital Heart Disease Studies (9 papers)Genetics and Neurodevelopmental Disorders (3 papers)
Cited by: Epidemiology Genetics Molecular Biology
Journals: PEDIATRICS International Journal of Molecular Sciences The American Journal of Human Genetics
Partner nations: United States Belgium Italy

In The Last Decade

Karlene Coleman

18 papers receiving 849 citations

Peers

Countries citing papers authored by Karlene Coleman

Since Specialization

Citations

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

Fields of papers citing papers by Karlene Coleman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karlene Coleman

This figure shows the co-authorship network connecting the top 25 collaborators of Karlene Coleman. A scholar is included among the top collaborators of Karlene Coleman 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 Karlene Coleman. Karlene Coleman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	The impact of concurrent X chromosome anomalies on diagnosis and bleeding phenotype in children with hemophilia: A single‐institution case series 2023 ·Pediatric Blood & Cancer ·(unknown),Karlene Coleman,Glaivy Batsuli	0
2	The emotional experience of mothers of children with haemophilia: maternal guilt, effective coping strategies and resilience within the haemophilia community 2023 ·Haemophilia ·(unknown),(unknown),(unknown),Karlene Coleman,Robert F. Sidonio	4
3	Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome 2017 ·International Journal of Molecular Sciences ·Opal Ousley,(unknown),Samuel Fernàndez‐Carriba,Erica Smearman,(unknown),Michael J. Morrier,David W. Evans,Karlene Coleman,Joseph F. Cubells	33
4	Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome 2015 ·The American Journal of Human Genetics ·Tingwei Guo,Jonathan H. Chung,Tao Wang,Donna M. McDonald‐McGinn,Wendy R. Kates,(unknown),Karlene Coleman,Elaine H. Zackai,Beverly S. Emanuel,Bernice E. Morrow	40
5	Whole-Genome Sequencing and Integrative Genomic Analysis Approach on Two 22q11.2 Deletion Syndrome Family Trios for Genotype to Phenotype Correlations 2015 ·Human Mutation ·Jonathan H. Chung,(unknown),(unknown),Zhengdong Zhang,Karlene Coleman,Bernice E. Morrow	14
6	Compound heterozygous mutations inNEK8in siblings with end‐stage renal disease with hepatic and cardiac anomalies 2015 ·American Journal of Medical Genetics Part A ·Ramakrishnan Rajagopalan,Christopher M. Grochowski,Melissa A. Gilbert,(unknown),Karlene Coleman,René Romero,Kathleen M. Loomes,David A. Piccoli,Marcella Devoto,Nancy B. Spinner	17
7	The effect of hypocalcemia in early childhood on autism-related social and communication skills in patients with 22q11 deletion syndrome 2014 ·European Archives of Psychiatry and Clinical Neuroscience ·(unknown),Opal Ousley,Lisa Kobrynski,(unknown),Matthew E. Oster,Samuel Fernàndez‐Carriba,Joseph F. Cubells,Karlene Coleman,Bradley D. Pearce	6
8	Association of IL-12p70 and IL-6:IL-10 ratio with autism-related behaviors in 22q11.2 deletion syndrome: A preliminary report 2013 ·Brain Behavior and Immunity ·Heather E. Ross,Ying Guo,Karlene Coleman,Opal Ousley,Andrew H. Miller	48
9	Severe aortopathy due to fibulin-4 deficiency: molecular insights, surgical strategy, and a review of the literature 2013 ·European Journal of Pediatrics ·Camden L. Hebson,Karlene Coleman,Martha L. Clabby,Denver Sallee,Suma P. Shankar,Bart Loeys,Lut Van Laer,(unknown)	13
10	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
11	Do Neonates with Genetic Abnormalities Have an Increased Morbidity and Mortality following Cardiac Surgery? 2009 ·Congenital Heart Disease ·Janet M. Simsic,Karlene Coleman,Kevin Maher,Angel R. Cuadrado,Paul M. Kirshbom	33
12	Preaxial hallucal polydactyly as a marker for diabetic embryopathy 2008 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Margaret P Adam,Louanne Hudgins,John C. Carey,Bryan D. Hall,Karlene Coleman,Karen W. Gripp,Antonio Pérez Aytés,John M. Graham	16
13	Sclerocornea associated with the chromosome 22q11.2 deletion syndrome 2008 ·American Journal of Medical Genetics Part A ·Gil Binenbaum,Donna M. McDonald‐McGinn,Elaine H. Zackai,(unknown),Karlene Coleman,(unknown),Margaret P Adam,Melanie Manning,Deborah Alcorn,(unknown),(unknown),Brian J. Forbes	22
14	A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: Implications for clinical evaluation and treatment 2007 ·Current Psychiatry Reports ·Opal Ousley,(unknown),Mary Lynn Dell,Karlene Coleman,Joseph F. Cubells	39
15	Rhabdomyomatous hamartomata of the pharyngeal region with bilateral microtia and aural atresia: A new association? 2006 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Margaret P Adam,Carlos R. Abramowsky,(unknown),Karlene Coleman,N. Wendell Todd	7
16	Deletion of chromosome 22q11.2 and outcome in patients with pulmonary atresia and ventricular septal defect 2003 ·The Annals of Thoracic Surgery ·William T. Mahle,(unknown),Karlene Coleman,Robert M. Campbell,Vincent K.H Tam,Robert Vincent,Kirk R. Kanter	66
17	A Population-Based Study of the 22q11.2 Deletion: Phenotype, Incidence, and Contribution to Major Birth Defects in the Population 2003 ·PEDIATRICS ·Lorenzo D. Botto,Kristin M. May,Paul M. Fernhoff,Adolfo Correa,Karlene Coleman,Sonja A. Rasmussen,Robert Merritt,Leslie A. O’Leary,Lee-Yang Wong,E. Marsha Elixson,William T. Mahle,Robert M. Campbell	481
18	Genetic Counseling in Congenital Heart Disease 2002 ·Critical Care Nursing Quarterly ·Karlene Coleman	8
19	Unique mosaicism of tetraploidy and trisomy 8: Clinical, cytogenetic, and molecular findings in a live-born infant 1996 ·American Journal of Medical Genetics ·Helen Roberts,Debra Saxe,Kasinathan Muralidharan,Karlene Coleman,(unknown),Paul M. Fernhoff	8

About Karlene Coleman

Karlene Coleman is a scholar working on Developmental Biology, Genetics and Epidemiology, having authored 19 papers that have together received 873 indexed citations. Recurring topics across this work include Congenital heart defects research (12 papers), Congenital Heart Disease Studies (9 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Epidemiology (422 citations), Genetics (330 citations) and Molecular Biology (643 citations). Karlene Coleman has collaborated with scholars based in United States, Belgium and Italy. Frequent co-authors include William T. Mahle, Robert M. Campbell, Paul M. Fernhoff, Kristin M. May, Robert Merritt, Lorenzo D. Botto, Leslie A. O’Leary, E. Marsha Elixson, Sonja A. Rasmussen and Lee-Yang Wong. Their work appears in journals such as PEDIATRICS, International Journal of Molecular Sciences and The American Journal of Human Genetics.

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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