Todd Ackley

1.1k total citations
10 papers, 207 citations indexed

About

Todd Ackley is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Todd Ackley has authored 10 papers receiving a total of 207 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Molecular Biology. Recurrent topics in Todd Ackley's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (3 papers) and Prenatal Screening and Diagnostics (3 papers). Todd Ackley is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (3 papers) and Prenatal Screening and Diagnostics (3 papers). Todd Ackley collaborates with scholars based in United States, Netherlands and Poland. Todd Ackley's co-authors include Ramaswamy K. Iyer, Leon Raskin, Carol R. Bradford, Marian Ludgate, Douglas R. Fullen, Timothy M. Johnson, Jeffrey W. Innis, Jirair K. Bedoyan, Ravinesh A. Kumar and Faye S. Silverstein and has published in prestigious journals such as The American Journal of Surgical Pathology, Methods in molecular biology and American Journal of Medical Genetics Part A.

In The Last Decade

Todd Ackley

9 papers receiving 193 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Todd Ackley United States 7 107 80 67 42 32 10 207
Magdalena Socha Poland 10 143 1.3× 113 1.4× 43 0.6× 17 0.4× 33 1.0× 24 260
Anna Hammarsjö Sweden 9 164 1.5× 115 1.4× 16 0.2× 59 1.4× 30 0.9× 21 264
Marilena Carmela Di Giacomo Italy 9 148 1.4× 140 1.8× 25 0.4× 14 0.3× 30 0.9× 14 278
Maria Paola Recalcati Italy 11 191 1.8× 240 3.0× 17 0.3× 49 1.2× 89 2.8× 21 378
Chureerat Phokaew Thailand 9 282 2.6× 67 0.8× 20 0.3× 58 1.4× 18 0.6× 21 367
Jennifer M. Huang United States 8 256 2.4× 160 2.0× 38 0.6× 35 0.8× 64 2.0× 12 330
Makia J. Marafie Kuwait 11 142 1.3× 154 1.9× 37 0.6× 79 1.9× 21 0.7× 28 279
Carrie M. Coleman United States 8 153 1.4× 84 1.1× 63 0.9× 56 1.3× 9 0.3× 10 294
Ali Awaji Saudi Arabia 4 178 1.7× 170 2.1× 27 0.4× 24 0.6× 10 0.3× 6 265
R Leśniewicz Poland 9 98 0.9× 154 1.9× 23 0.3× 24 0.6× 47 1.5× 20 347

Countries citing papers authored by Todd Ackley

Since Specialization
Citations

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

Fields of papers citing papers by Todd Ackley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Todd Ackley

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

All Works

10 of 10 papers shown
1.
Kang, Benjamin, Hong Xiao, Todd Ackley, & Lina Shao. (2024). Cancer Sample Analysis Utilizing Single-Nucleotide Polymorphism Array and Array Comparative Genomic Hybridization. Methods in molecular biology. 2825. 151–171.
2.
3.
Soemedi, Rachel, Jonathan M. Levine, Sarah Geisler, et al.. (2014). Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development. Congenital Heart Disease. 10(3). 193–208. 21 indexed citations
4.
Quinonez, Shane C., Peter Hedera, Mason Barr, et al.. (2012). Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings. American Journal of Medical Genetics Part A. 158A(10). 2591–2601. 18 indexed citations
5.
Raskin, Leon, Marian Ludgate, Ramaswamy K. Iyer, et al.. (2011). Copy Number Variations and Clinical Outcome in Atypical Spitz Tumors. The American Journal of Surgical Pathology. 35(2). 243–252. 75 indexed citations
6.
Nelson, Marc E., Shane C. Quinonez, Todd Ackley, Ram Iyer, & Jeffrey W. Innis. (2011). Multiple congenital anomalies and developmental delay in a boy associated with a de novo 16p13.3 deletion. American Journal of Medical Genetics Part A. 155(3). 612–617. 6 indexed citations
7.
Otto, Edgar A., Friedhelm Hildebrandt, Todd Ackley, et al.. (2011). Exome capture and massively parallel sequencing identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome. Journal of Pediatric Urology. 7(5). 569–573. 16 indexed citations
8.
Vlangos, Christopher N., Todd Ackley, Hans van Bokhoven, et al.. (2010). Comprehensive genetic analysis of OEIS complex reveals no evidence for a recurrent microdeletion or duplication. American Journal of Medical Genetics Part A. 155(1). 38–49. 21 indexed citations
9.
Bedoyan, Jirair K., Ravinesh A. Kumar, Jyotsna Sudi, et al.. (2010). Duplication 16p11.2 in a child with infantile seizure disorder. American Journal of Medical Genetics Part A. 152A(6). 1567–1574. 37 indexed citations
10.
Bedoyan, Jirair K., Marci M. Lesperance, Todd Ackley, et al.. (2010). A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia. American Journal of Medical Genetics Part A. 155(1). 154–163. 12 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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