K. Morgan

1.6k total citations
28 papers, 1.2k citations indexed

About

K. Morgan is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, K. Morgan has authored 28 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in K. Morgan's work include Epigenetics and DNA Methylation (5 papers), Genetic Syndromes and Imprinting (3 papers) and Cystic Fibrosis Research Advances (3 papers). K. Morgan is often cited by papers focused on Epigenetics and DNA Methylation (5 papers), Genetic Syndromes and Imprinting (3 papers) and Cystic Fibrosis Research Advances (3 papers). K. Morgan collaborates with scholars based in Canada, United States and Belgium. K. Morgan's co-authors include Carmen Sapienza, Takuya Fujiwara, Fereshteh Ghavimi, Mark A. Lovell, Heidi Scrable, Webster K. Cavenee, Mikołaj Łabuda, Francis H. Glorieux, Johanna M. Rommens and Mark H. Skolnick and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

K. Morgan

28 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
K. Morgan Canada 14 665 541 220 174 129 28 1.2k
Luis E. Figuera Mexico 23 637 1.0× 622 1.1× 69 0.3× 101 0.6× 87 0.7× 134 1.8k
Takuya Naruto Japan 23 588 0.9× 423 0.8× 122 0.6× 95 0.5× 71 0.6× 110 1.6k
Aoife Waters United Kingdom 18 625 0.9× 556 1.0× 111 0.5× 114 0.7× 85 0.7× 36 1.6k
Michał Witt Poland 25 690 1.0× 671 1.2× 607 2.8× 49 0.3× 81 0.6× 87 1.7k
Ariadni Mavrou Greece 24 626 0.9× 458 0.8× 134 0.6× 51 0.3× 112 0.9× 94 1.7k
Miranda R.M. Baert Netherlands 23 694 1.0× 194 0.4× 121 0.6× 69 0.4× 134 1.0× 32 1.7k
Hideaki Sawai Japan 17 482 0.7× 305 0.6× 75 0.3× 214 1.2× 40 0.3× 67 1.2k
Hans‐Hartmut Peter Germany 25 359 0.5× 398 0.7× 210 1.0× 96 0.6× 247 1.9× 58 2.3k
Vojtěch Thon Czechia 22 283 0.4× 506 0.9× 331 1.5× 70 0.4× 192 1.5× 58 1.9k
Éva Oláh Hungary 19 358 0.5× 187 0.3× 63 0.3× 87 0.5× 97 0.8× 85 1.1k

Countries citing papers authored by K. Morgan

Since Specialization
Citations

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

Fields of papers citing papers by K. Morgan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. Morgan

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

All Works

20 of 20 papers shown
1.
Morgan, K., Kulsoom Abdullah, Joseph Y. Lo, et al.. (2024). A Method for Efficient De-identification of DICOM Metadata and Burned-in Pixel Text. Journal of Imaging Informatics in Medicine. 37(5). 1–7. 1 indexed citations
2.
Guillot, Loïc, et al.. (2008). Sex differences in the genetic architecture of susceptibility to Cryptococcus neoformans pulmonary infection. Genes and Immunity. 9(6). 536–545. 13 indexed citations
3.
Loredo‐Osti, J. Concepción, et al.. (2006). Complex genetic control of susceptibility to Mycobacterium bovis (Bacille Calmette-Guérin) infection in wild-derived Mus spretus mice. Genes and Immunity. 7(8). 684–687. 11 indexed citations
4.
Loredo‐Osti, Jorge, et al.. (2005). Mapping of interactions and mouse congenic strains identified novel epistatic QTLs controlling the persistence of Salmonella Enteritidis in mice. Genes and Immunity. 6(6). 500–508. 12 indexed citations
5.
Lowry, R. Brian, A. Micheil Innes, François P. Bernier, et al.. (2003). Bowen–Conradi syndrome: A clinical and genetic study. American Journal of Medical Genetics Part A. 120A(3). 423–428. 21 indexed citations
6.
Greenwood, Celia M.T., Alexandre Bureau, Jorge Loredo‐Osti, et al.. (2001). Identity-by-descent sharing using Markov chain Monte Carlo in subsets of the asthma Hutterite pedigree. Genetic Epidemiology. 244–251. 1 indexed citations
7.
Naumova, Anna K., M. Leppert, David F. Barker, K. Morgan, & Carmen Sapienza. (1998). Parental Origin–Dependent, Male Offspring–Specific Transmission-Ratio Distortion at Loci on the Human X Chromosome. The American Journal of Human Genetics. 62(6). 1493–1499. 54 indexed citations
8.
Turecki, Gustavo, et al.. (1996). A systematic evaluation of linkage studies in bipolar disorder. Acta Psychiatrica Scandinavica. 93(5). 317–326. 11 indexed citations
9.
Liu, Jie, Takuya Fujiwara, Fabio Orlando Neira Sánchez, et al.. (1995). Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene.. PubMed. 56(4). 845–53. 145 indexed citations
10.
Pausová, Zdenka, K. Morgan, Takuya Fujiwara, & Geoffrey N. Hendy. (1995). Evolution of a repeat sequence in the parathyroid hormone-related peptide gene in primates. Mammalian Genome. 6(6). 408–414. 3 indexed citations
11.
Wirth, Brunhilde, Eric Hahnen, K. Morgan, et al.. (1995). Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAs. Human Molecular Genetics. 4(8). 1273–1284. 87 indexed citations
12.
Morgan, K., et al.. (1994). A candidate gene approach for the genetic analysis of susceptibility to tuberculosis. The American Journal of Human Genetics. 55. 1 indexed citations
13.
Simard, Jacques, Patricia N. Tonin, Francine Durocher, et al.. (1994). Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families. Nature Genetics. 8(4). 392–398. 264 indexed citations
14.
Bichet, Daniel G., Marie‐Françoise Arthus, Michèle Lonergan, et al.. (1993). X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesis.. Journal of Clinical Investigation. 92(3). 1262–1268. 110 indexed citations
15.
Sapienza, Carmen, et al.. (1992). The polar-lethal Ovum mutant gene maps to the distal portion of mouse chromosome 11.. Genetics. 132(1). 241–246. 50 indexed citations
16.
Fung, Ernest, et al.. (1991). Dihydropyrimidine Dehydrogenase Deficiency in a Hutterite Newborn. Advances in experimental medicine and biology. 309B. 311–314. 2 indexed citations
17.
Thompson, E. A. & K. Morgan. (1989). Recursive descent probabilities for rare recessive lethals. Annals of Human Genetics. 53(4). 357–374. 10 indexed citations
18.
Fujiwara, Takuya, K. Morgan, Robert H. Schwartz, et al.. (1989). Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren.. PubMed. 44(3). 327–37. 30 indexed citations
19.
Pearce, W G, et al.. (1987). Autosomal recessive juvenile cataract in Hutterites. Ophthalmic Paediatrics and Genetics. 8(2). 119–124. 10 indexed citations
20.
Lowry, R. Brian, et al.. (1985). Congenital anomalies in the Hutterite population: A preliminary survey and hypothesis. American Journal of Medical Genetics. 22(3). 545–552. 18 indexed citations

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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