Joannella Morales

14.0k total citations · 2 hit papers
12 papers, 3.6k citations indexed

About

Joannella Morales is a scholar working on Genetics, Molecular Biology and Organic Chemistry. According to data from OpenAlex, Joannella Morales has authored 12 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 1 paper in Organic Chemistry. Recurrent topics in Joannella Morales's work include Genomics and Rare Diseases (5 papers), Genetic Associations and Epidemiology (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Joannella Morales is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetic Associations and Epidemiology (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Joannella Morales collaborates with scholars based in United States, United Kingdom and Netherlands. Joannella Morales's co-authors include Paul Flicek, Jacqueline A. L. MacArthur, Lucia A. Hindorff, Danielle Welter, Heather Junkins, Helen Parkinson, Peggy Hall, Tony Burdett, Teri A. Manolio and Fiona Cunningham and has published in prestigious journals such as Nucleic Acids Research, Neuron and Journal of Neuroscience.

In The Last Decade

Joannella Morales

11 papers receiving 3.6k 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.

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

2013 1.9k citations Danielle Welter, Jacqueline A. L. MacArthur et al. Nucleic Acids Research profile →
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)

2016 1.3k citations Jacqueline A. L. MacArthur, Emily Bowler-Barnett et al. Nucleic Acids Research profile →

Peers

Countries citing papers authored by Joannella Morales

Since Specialization

Citations

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

Fields of papers citing papers by Joannella Morales

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joannella Morales

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

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Design and implementation of an action plan for justice, equity, diversity, and inclusion within the Clinical Genome Resource 2025 ·The American Journal of Human Genetics ·Alice B. Popejoy, Deborah Ritter, Danielle R. Azzariti, Jonathan S. Berg, Joanna E. Bulkley, Mildred K. Cho, Claudia Gonzaga‐Jauregui, Teri E. Klein, Daphne Oluwaseun Martschenko, Akinyemi Oni‐Orisan, Erin M. Ramos, Heidi L. Rehm, Erin Rooney Riggs, Matt W. Wright, Michael Yudell, Sharon E. Plon, Joannella Morales	0
2	Patterns of pharmacogenetic variation in nine biogeographic groups 2024 ·Clinical and Translational Science ·(unknown), Lucia A. Hindorff, Joannella Morales, Erin M. Ramos, Teri A. Manolio	2
3	The value of primary transcripts to the clinical and non‐clinical genomics community: Survey results and roadmap for improvements 2021 ·Molecular Genetics & Genomic Medicine ·Joannella Morales, Aoife McMahon, Jane Loveland, Emily Perry, Adam Frankish, Sarah Hunt, Irina M. Armean, Paul Flicek, Fiona Cunningham	3
4	User-focused development of the NHGRI-EBI Genome-Wide Association Studies Catalog 2019 ·Faculty of 1000 Research Ltd ·Elliot Sollis, Annalisa Buniello, María Cerezo, Peggy Hall, Laura W. Harris, James Hayhurst, Heather Junkins, Elizabeth Lewis, Claudio Malangone, Aoife McMahon, Joannella Morales, Dániel Süveges, Olga Vrousgou, Patricia L. Whetzel, Paul Flicek, Lucia A. Hindorff, Fiona Cunningham, Tony Burdett, Helen Parkinson, Jacqueline A. L. MacArthur	1
5	Curated disease‐causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH 2019 ·Journal of Thrombosis and Haemostasis ·Karyn Mégy, Kate Downes, Ilenia Simeoni, Loredana Bury, Joannella Morales, Rutendo Mapeta, Daniel B. Bellissimo, Paul F. Bray, Anne Goodeve, Paolo Gresele, Michele P. Lambert, Pieter H. Reitsma, Willem H. Ouwehand, Kathleen Freson	56
6	The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog) breakdown → 2016 ·Nucleic Acids Research ·Jacqueline A. L. MacArthur, Emily Bowler-Barnett, María Cerezo, Laurent Gil, Peggy Hall, Emma Hastings, Heather Junkins, Aoife McMahon, Annalisa Milano, Joannella Morales, Zoë May Pendlington, Danielle Welter, Tony Burdett, Lucia A. Hindorff, Paul Flicek, Fiona Cunningham, Helen Parkinson	1346
7	Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains 2016 ·Epigenetics ·David Monk, Joannella Morales, Johan T. den Dunnen, Silvia Russo, Franck Court, Dirk Prawitt, (unknown), Jasmin Beygo, Karin Buiting, Zeynep Tümer, (unknown)	70
8	Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants 2013 ·Nucleic Acids Research ·Jacqueline A. L. MacArthur, Joannella Morales, (unknown), Alex Astashyn, Laurent Gil, Elspeth A. Bruford, Pontus Larsson, Paul Flicek, Raymond Dalgleish, Donna Maglott, Fiona Cunningham	45
9	The NHGRI GWAS Catalog, a curated resource of SNP-trait associations breakdown → 2013 ·Nucleic Acids Research ·Danielle Welter, Jacqueline A. L. MacArthur, Joannella Morales, Tony Burdett, Peggy Hall, Heather Junkins, (unknown), Paul Flicek, Teri A. Manolio, Lucia A. Hindorff, Helen Parkinson	1850
10	TheDrosophilaFMRP and LARK RNA-Binding Proteins Function Together to Regulate Eye Development and Circadian Behavior 2008 ·Journal of Neuroscience ·(unknown), Vasudha Sundram, Fanny Ng, Yelena Kleyner, Joannella Morales, Juan Botas, F. Rob Jackson, David L. Nelson	27
11	Drosophila Fragile X Protein, DFXR, Regulates Neuronal Morphology and Function in the Brain 2002 ·Neuron ·Joannella Morales, P. Robin Hiesinger, Andrew J. Schroeder, Kazuhiko Kume, Patrik Verstreken, F. Rob Jackson, David L. Nelson, Bassem A. Hassan	199
12	Identification of Developmentally Regulated Sea Urchin U5 snRNA Genes 1997 ·DNA sequence ·Joannella Morales, (unknown), Jan L. Sumerel, (unknown)	7

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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