Monica B. Proud

1.3k total citations
4 papers, 247 citations indexed

About

Monica B. Proud is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Monica B. Proud has authored 4 papers receiving a total of 247 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Cognitive Neuroscience. Recurrent topics in Monica B. Proud's work include Genomic variations and chromosomal abnormalities (2 papers), Autism Spectrum Disorder Research (2 papers) and Prenatal Screening and Diagnostics (1 paper). Monica B. Proud is often cited by papers focused on Genomic variations and chromosomal abnormalities (2 papers), Autism Spectrum Disorder Research (2 papers) and Prenatal Screening and Diagnostics (1 paper). Monica B. Proud collaborates with scholars based in United States and Canada. Monica B. Proud's co-authors include Qixuan Chen, Sudha Kilaru Kessler, Elysa J. Marco, Melissa B. Ramocki, Sarah Spence, LeeAnne Green Snyder, Kyle J. Steinman, Elliott H. Sherr, Debra D’Angelo and Wendy K. Chung and has published in prestigious journals such as European Journal of Human Genetics, American Journal of Medical Genetics Part A and Clinical Pediatrics.

In The Last Decade

Monica B. Proud

4 papers receiving 232 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Monica B. Proud United States 4 174 123 73 33 20 4 247
Lisa M. Prock United States 2 333 1.9× 96 0.8× 115 1.6× 35 1.1× 21 1.1× 2 384
Jamie Love‐Nichols United States 3 335 1.9× 90 0.7× 113 1.5× 41 1.2× 20 1.0× 3 388
Jin Szatkiewicz United States 11 220 1.3× 125 1.0× 40 0.5× 22 0.7× 26 1.3× 30 321
Tianyun Wang China 8 97 0.6× 71 0.6× 89 1.2× 29 0.9× 9 0.5× 15 205
Amber Boys Australia 7 154 0.9× 143 1.2× 41 0.6× 35 1.1× 11 0.6× 10 281
J.A.S. Vorstman Netherlands 4 225 1.3× 141 1.1× 133 1.8× 23 0.7× 5 0.3× 4 298
Bert Ba de Vries Netherlands 5 270 1.6× 169 1.4× 121 1.7× 17 0.5× 7 0.3× 7 305
Sharon Bade Shrestha United States 7 88 0.5× 71 0.6× 106 1.5× 12 0.4× 7 0.3× 8 255
Wei‐Hsien Chien Taiwan 8 145 0.8× 72 0.6× 145 2.0× 20 0.6× 5 0.3× 14 257
Charlly Kao United States 10 106 0.6× 107 0.9× 40 0.5× 24 0.7× 20 1.0× 20 233

Countries citing papers authored by Monica B. Proud

Since Specialization
Citations

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

Fields of papers citing papers by Monica B. Proud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Monica B. Proud. 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 Monica B. Proud. The network helps show where Monica B. Proud may publish in the future.

Co-authorship network of co-authors of Monica B. Proud

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

All Works

4 of 4 papers shown
1.
Steinman, Kyle J., Sarah Spence, Melissa B. Ramocki, et al.. (2016). 16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort. American Journal of Medical Genetics Part A. 170(11). 2943–2955. 135 indexed citations
2.
Monteiro, Sónia, Diane Treadwell‐Deering, Leandra N. Berry, et al.. (2015). Prevalence of Autism Spectrum Disorder in Children Referred for Diagnostic Autism Evaluation. Clinical Pediatrics. 54(14). 1322–1327. 26 indexed citations
3.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Carolyn Bay, et al.. (2011). Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43–q44. European Journal of Human Genetics. 20(2). 176–179. 38 indexed citations
4.
Beck, T., et al.. (2009). A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder. American Journal of Medical Genetics Part A. 149A(8). 1758–1762. 48 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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