Bernice E. Morrow

16.5k total citations · 1 hit paper
147 papers, 8.5k citations indexed

About

Bernice E. Morrow is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Bernice E. Morrow has authored 147 papers receiving a total of 8.5k indexed citations (citations by other indexed papers that have themselves been cited), including 122 papers in Molecular Biology, 55 papers in Genetics and 36 papers in Epidemiology. Recurrent topics in Bernice E. Morrow's work include Congenital heart defects research (95 papers), Genomic variations and chromosomal abnormalities (33 papers) and Congenital Heart Disease Studies (32 papers). Bernice E. Morrow is often cited by papers focused on Congenital heart defects research (95 papers), Genomic variations and chromosomal abnormalities (33 papers) and Congenital Heart Disease Studies (32 papers). Bernice E. Morrow collaborates with scholars based in United States, United Kingdom and Canada. Bernice E. Morrow's co-authors include Rosalie Goldberg, Robert J. Shprintzen, David R. Soll, Jonathan R. Warner, Raju Kucherlapati, Peter Scambler, Raj K. Pandita, Jun Liao, Qida Ju and Lisa Edelmann and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Bernice E. Morrow

145 papers receiving 8.3k 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.

22q11.2 deletion syndrome

2015 791 citations Donna M. McDonald‐McGinn, Ann Swillen et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bernice E. Morrow United States	47	6.2k	3.3k	2.0k	1.1k	767	147	8.5k
David Fitzpatrick United Kingdom	65	6.9k 1.1×	5.4k 1.6×	1.1k 0.6×	729 0.6×	452 0.6×	271	14.3k
Chad A. Shaw United States	65	7.7k 1.2×	5.7k 1.7×	864 0.4×	471 0.4×	1.2k 1.6×	193	13.9k
William H Colledge United Kingdom	61	9.6k 1.5×	3.3k 1.0×	497 0.3×	1.7k 1.5×	346 0.5×	172	16.5k
Joris Vermeesch Belgium	59	6.6k 1.1×	6.4k 1.9×	1.1k 0.6×	1.0k 0.9×	2.0k 2.5×	381	13.3k
Christine A. Kozak United States	65	9.1k 1.5×	3.0k 0.9×	860 0.4×	232 0.2×	815 1.1×	329	14.4k
C. Geoffrey Woods United Kingdom	48	6.8k 1.1×	3.4k 1.0×	556 0.3×	206 0.2×	700 0.9×	97	11.0k
Eric D. Green United States	36	3.8k 0.6×	1.5k 0.5×	499 0.3×	268 0.2×	397 0.5×	65	7.7k
Terry Magnuson United States	70	12.5k 2.0×	4.2k 1.3×	473 0.2×	500 0.4×	717 0.9×	198	18.0k
Karen J. Moore United States	33	4.4k 0.7×	1.7k 0.5×	1.6k 0.8×	251 0.2×	301 0.4×	68	10.5k
Suzanne M. Leal United States	47	5.0k 0.8×	4.7k 1.4×	591 0.3×	825 0.7×	305 0.4×	211	10.8k

Countries citing papers authored by Bernice E. Morrow

Since Specialization

Citations

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

Fields of papers citing papers by Bernice E. Morrow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernice E. Morrow. 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 Bernice E. Morrow. The network helps show where Bernice E. Morrow may publish in the future.

Co-authorship network of co-authors of Bernice E. Morrow

This figure shows the co-authorship network connecting the top 25 collaborators of Bernice E. Morrow. A scholar is included among the top collaborators of Bernice E. Morrow 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 Bernice E. Morrow. Bernice E. Morrow 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

Morrow, Bernice E., et al.. (2026). Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome. medRxiv.

Nomaru, Hiroko, David M. Reynolds, Robert Dubin, et al.. (2023). An optimized approach for multiplexing single-nuclear ATAC-seq using oligonucleotide-conjugated antibodies. Epigenetics & Chromatin. 16(1). 14–14. 2 indexed citations

Wu, Bingruo, Pengfei Lu, Tae‐Ju Park, et al.. (2023). Crk and Crkl Are Required in the Endocardial Lineage for Heart Valve Development. Journal of the American Heart Association. 12(18). e029683–e029683. 2 indexed citations

Campbell, Ian M., T. Blaine Crowley, Chintan Jobaliya, et al.. (2022). Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression. Clinical Genetics. 103(1). 109–113. 4 indexed citations

McGinn, Daniel E., T. Blaine Crowley, Tracy Heung, et al.. (2022). Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome. Genes. 13(10). 1800–1800. 2 indexed citations

Mitchell, Laura E., Elizabeth Goldmuntz, Hongbo Xie, et al.. (2021). Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States. Genes. 12(7). 1030–1030.

Agopian, A. J., Elizabeth Goldmuntz, Håkon Håkonarson, et al.. (2021). Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects. Genes. 12(5). 655–655. 2 indexed citations

Nomaru, Hiroko, Yang Liu, Christopher De Bono, et al.. (2021). Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm. Nature Communications. 12(1). 6645–6645. 32 indexed citations

Liu, Yang, Pengfei Lu, Yidong Wang, et al.. (2019). Spatiotemporal Gene Coexpression and Regulation in Mouse Cardiomyocytes of Early Cardiac Morphogenesis. Journal of the American Heart Association. 8(15). e012941–e012941. 10 indexed citations

10.

Mostovoy, Yulia, Feyza Yilmaz, Steven Pastor, et al.. (2019). The 22q11 low copy repeats are characterized by unprecedented size and structural variability. Genome Research. 29(9). 1389–1401. 28 indexed citations

11.

Racedo, Silvia E., Mingyan Lin, Tingwei Guo, et al.. (2017). Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome. PLoS Genetics. 13(3). e1006687–e1006687. 20 indexed citations

12.

Guo, Chaoshe, Ye Sun, Bin Zhou, et al.. (2011). A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis. Journal of Clinical Investigation. 121(4). 1585–1595. 104 indexed citations

13.

Funke, Birgit, Marco Ramoni, Christine Finn, et al.. (2007). A Novel, Single Nucleotide Polymorphism-Based Assay to Detect 22q11 Deletions. Genetic Testing. 11(1). 91–100. 5 indexed citations

14.

Nowotschin, Sonja, Jun Liao, Philip J. Gage, et al.. (2006). Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field. Development. 133(8). 1565–1573. 108 indexed citations

15.

McDermid, Heather E. & Bernice E. Morrow. (2002). Genomic Disorders on 22q11. The American Journal of Human Genetics. 70(5). 1077–1088. 182 indexed citations

16.

Edelmann, Lisa, Elizabeth Spiteri, Rosalie Goldberg, et al.. (1999). A Common Breakpoint on 11q23 in Carriers of the Constitutional t(11;22) Translocation. The American Journal of Human Genetics. 65(6). 1608–1616. 46 indexed citations

17.

O‘Donnell, Hilary, et al.. (1997). Detection of a deletion within 22q11 which has no overlap with the DiGeorge syndrome critical region. UCL Discovery (University College London). 2 indexed citations

18.

Funke, Birgit, Bruno Saint-Jore, Anne Puech, et al.. (1997). Characterization and Mutation Analysis of Goosecoid-like (GSCL), a Homeodomain-Containing Gene That Maps to the Critical Region for VCFS/DGS on 22q11. Genomics. 46(3). 364–372. 21 indexed citations

19.

Morrow, Bernice E., Stewart P. Johnson, & Jonathan R. Warner. (1993). The rRNA Enhancer Regulates rRNA Transcription in Saccharomyces cerevisiae. Molecular and Cellular Biology. 13(2). 1283–1289. 8 indexed citations

20.

Ju, Qida, Bernice E. Morrow, & Jonathan R. Warner. (1990). REB1, a Yeast DNA-Binding Protein with Many Targets, Is Essential for Cell Growth and Bears Some Resemblance to the Oncogene myb. Molecular and Cellular Biology. 10(10). 5226–5234. 42 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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