Daniel J. Driscoll

10.9k total citations · 1 hit paper
104 papers, 6.8k citations indexed

About

Daniel J. Driscoll is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Daniel J. Driscoll has authored 104 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 92 papers in Genetics, 58 papers in Molecular Biology and 34 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Daniel J. Driscoll's work include Genetic Syndromes and Imprinting (84 papers), Epigenetics and DNA Methylation (49 papers) and Prenatal Screening and Diagnostics (34 papers). Daniel J. Driscoll is often cited by papers focused on Genetic Syndromes and Imprinting (84 papers), Epigenetics and DNA Methylation (49 papers) and Prenatal Screening and Diagnostics (34 papers). Daniel J. Driscoll collaborates with scholars based in United States, United Kingdom and Germany. Daniel J. Driscoll's co-authors include Suzanne B. Cassidy, Jennifer Miller, Stuart Schwartz, Robert D. Nicholls, Merlin G. Butler, Christopher C. Glenn, Charles A. Williams, Shinji Saitoh, M T Jong and Jonathan J. Shuster and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Daniel J. Driscoll

102 papers receiving 6.6k 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.

Prader-Willi syndrome

2012 1.0k citations Suzanne B. Cassidy, Jennifer Miller et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Daniel J. Driscoll United States	38	5.5k	4.0k	2.0k	508	391	104	6.8k
Suzanne B. Cassidy United States	38	5.9k 1.1×	2.8k 0.7×	2.0k 1.0×	697 1.4×	793 2.0×	107	7.0k
Jill A. Rosenfeld United States	42	3.6k 0.7×	2.9k 0.7×	1.3k 0.7×	433 0.9×	599 1.5×	174	5.9k
Carlos A. Bacino United States	38	3.1k 0.6×	2.4k 0.6×	934 0.5×	405 0.8×	322 0.8×	134	5.0k
Jozef Gécz Australia	56	5.9k 1.1×	6.6k 1.6×	804 0.4×	312 0.6×	1.1k 2.7×	232	10.5k
Bert B.A. de Vries Netherlands	39	5.1k 0.9×	3.6k 0.9×	785 0.4×	523 1.0×	653 1.7×	114	7.4k
Ignatia B. Van den Veyver United States	30	4.7k 0.9×	3.4k 0.9×	1.6k 0.8×	263 0.5×	1.9k 4.9×	105	6.7k
Thomas Eggermann Germany	44	4.5k 0.8×	4.2k 1.0×	2.5k 1.3×	497 1.0×	385 1.0×	299	7.0k
Karen Brøndum‐Nielsen Denmark	34	2.0k 0.4×	2.3k 0.6×	485 0.2×	233 0.5×	514 1.3×	137	4.1k
Trilochan Sahoo United States	36	2.8k 0.5×	1.9k 0.5×	1.1k 0.6×	222 0.4×	426 1.1×	67	4.1k
Ivo J.P. Arnhold Brazil	44	2.7k 0.5×	3.5k 0.9×	412 0.2×	511 1.0×	101 0.3×	186	6.1k

Countries citing papers authored by Daniel J. Driscoll

Since Specialization

Citations

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

Fields of papers citing papers by Daniel J. Driscoll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel J. Driscoll. 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 Daniel J. Driscoll. The network helps show where Daniel J. Driscoll may publish in the future.

Co-authorship network of co-authors of Daniel J. Driscoll

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel J. Driscoll. A scholar is included among the top collaborators of Daniel J. Driscoll 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 Daniel J. Driscoll. Daniel J. Driscoll 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

Kweh, Frederick, Carlos R. Sulsona, Jennifer Miller, & Daniel J. Driscoll. (2023). Hyperinsulinemia is a probable trigger for weight gain and hyperphagia in individuals with Prader‐Willi syndrome. Obesity Science & Practice. 9(4). 383–394. 2 indexed citations

Butler, Merlin G., Pamela Flodman, June‐Anne Gold, et al.. (2022). Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader–Willi Syndrome. Journal of Clinical Medicine. 11(9). 2572–2572. 3 indexed citations

Butler, Merlin G., Pamela Flodman, June‐Anne Gold, et al.. (2021). Influence of molecular classes and growth hormone treatment on growth and dysmorphology in Prader‐Willi syndrome: A multicenter study. Clinical Genetics. 100(1). 29–39. 9 indexed citations

Osann, Kathryn, et al.. (2020). Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome. Genes. 11(11). 1250–1250. 6 indexed citations

Burnett, Lisa C., Charles A. LeDuc, Carlos R. Sulsona, et al.. (2016). Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS. Stem Cell Research. 17(3). 526–530. 22 indexed citations

Butler, Merlin G., Waheeda A. Hossain, Carlos R. Sulsona, Daniel J. Driscoll, & Ann M. Manzardo. (2015). Increased plasma chemokine levels in children with Prader–Willi syndrome. American Journal of Medical Genetics Part A. 167(3). 563–571. 16 indexed citations

Buiting, Karin, Suzanne B. Cassidy, Daniel J. Driscoll, et al.. (2014). Clinical utility gene card for: Prader-Willi Syndrome. European Journal of Human Genetics. 22(9). 1153–1153. 15 indexed citations

Gold, June-Anne, Kathryn Osann, Pamela Flodman, et al.. (2013). Frequency of Prader–Willi syndrome in births conceived via assisted reproductive technology. Genetics in Medicine. 16(2). 164–169. 15 indexed citations

Wirth, Eva K., et al.. (2012). SECISBP2 syndrome: Mouse models for an atypical form of resistance to thyroid hormone. 15th International & 14th European Congress of Endocrinology. 29. 1 indexed citations

10.

Miller, Jennifer, Jessica A. Couch, Christiana M. Leonard, et al.. (2007). Sylvian fissure morphology in Prader-Willi syndrome and early-onset morbid obesity. Genetics in Medicine. 9(8). 536–543. 14 indexed citations

11.

Miller, Jennifer, Anthony P. Goldstone, Jessica A. Couch, et al.. (2007). Pituitary abnormalities in Prader–Willi syndrome and early onset morbid obesity. American Journal of Medical Genetics Part A. 146A(5). 570–577. 56 indexed citations

12.

Bittel, Douglas C., Nataliya Kibiryeva, Steven G. McNulty, et al.. (2006). Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader–Willi syndrome. American Journal of Medical Genetics Part A. 143A(5). 422–429. 24 indexed citations

13.

Bittel, Douglas C., Nataliya Kibiryeva, Zohreh Talebizadeh, Daniel J. Driscoll, & Merlin G. Butler. (2004). Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD. Genomics. 85(1). 85–91. 22 indexed citations

14.

Shapira, Nathan A., Mary Lessig, Tanya K. Murphy, Daniel J. Driscoll, & Wayne K. Goodman. (2002). Topiramate attenuates self-injurious behaviour in Prader–Willi syndrome. The International Journal of Neuropsychopharmacology. 5(2). 141–5. 50 indexed citations

15.

Jong, M T, Todd A. Gray, Yazhong Ji, et al.. (1999). A Novel Imprinted Gene, Encoding a RING Zinc-Finger Protein, and Overlapping Antisense Transcript in the Prader-Willi Syndrome Critical Region. Human Molecular Genetics. 8(5). 783–793. 184 indexed citations

16.

Mowery‐Rushton, Patricia, Daniel J. Driscoll, Robert D. Nicholls, Joseph Locker, & Urvashi Surti. (1996). DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi region. American Journal of Medical Genetics. 61(2). 140–146. 16 indexed citations

17.

Zackowski, Joleen L., Robert D. Nicholls, Brian A. Gray, et al.. (1993). Cytogenetic and molecular analysis in Angelman syndrome. American Journal of Medical Genetics. 46(1). 7–11. 28 indexed citations

18.

Glenn, Christopher C., et al.. (1993). Functional imprinting and epigenetic modification of the human SNRPN gene. Human Molecular Genetics. 2(12). 2001–2005. 132 indexed citations

19.

Migeon, Barbara R., Mitchell M. Holland, Daniel J. Driscoll, & J. Courtland Robinson. (1991). Programmed demethylation in CpG islands during human fetal development. Somatic Cell and Molecular Genetics. 17(2). 159–168. 24 indexed citations

20.

Driscoll, Daniel J. & Barbara R. Migeon. (1990). Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations. Somatic Cell and Molecular Genetics. 16(3). 267–282. 139 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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