Tim Donlon

1.7k total citations
26 papers, 1.3k citations indexed

About

Tim Donlon is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tim Donlon has authored 26 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tim Donlon's work include Genetic Syndromes and Imprinting (4 papers), Prenatal Screening and Diagnostics (4 papers) and Microtubule and mitosis dynamics (3 papers). Tim Donlon is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Prenatal Screening and Diagnostics (4 papers) and Microtubule and mitosis dynamics (3 papers). Tim Donlon collaborates with scholars based in United States, Switzerland and Canada. Tim Donlon's co-authors include Marc Lalande, S.A. Latt, Uta Francke, Tayfun Özçelık, Albert Schinzel, M. Lalande, Wendy P. Robinson, Stuart E. Leff, G.A.P. Bruns and Arnon Nagler and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Tim Donlon

25 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tim Donlon United States 18 672 607 254 201 139 26 1.3k
M. H. K. Shokeir Canada 19 355 0.5× 557 0.9× 178 0.7× 88 0.4× 153 1.1× 48 1.3k
Hai‐Yang Law Singapore 21 334 0.5× 444 0.7× 385 1.5× 265 1.3× 46 0.3× 54 1.6k
Arabella Smith Australia 22 1.2k 1.7× 605 1.0× 591 2.3× 107 0.5× 50 0.4× 119 1.8k
Ashwin Dalal India 20 543 0.8× 651 1.1× 202 0.8× 52 0.3× 52 0.4× 151 1.4k
Gökçe Törüner United States 19 376 0.6× 581 1.0× 90 0.4× 140 0.7× 213 1.5× 86 1.4k
Gail E. Graham Canada 23 549 0.8× 786 1.3× 147 0.6× 42 0.2× 163 1.2× 60 1.9k
M O Rethoré France 21 754 1.1× 599 1.0× 395 1.6× 47 0.2× 33 0.2× 62 1.5k
Bradley W. Popovich United States 19 947 1.4× 802 1.3× 174 0.7× 95 0.5× 20 0.1× 28 1.7k
M Gautier France 16 498 0.7× 396 0.7× 237 0.9× 42 0.2× 138 1.0× 60 1.7k
Elizabeth M. Rohlfs United States 18 435 0.6× 705 1.2× 149 0.6× 91 0.5× 40 0.3× 25 1.8k

Countries citing papers authored by Tim Donlon

Since Specialization
Citations

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

Fields of papers citing papers by Tim Donlon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tim Donlon

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

All Works

20 of 20 papers shown
1.
Maguire, Patricia B., Tim Donlon, Martin Parsons, et al.. (2018). Proteomic Analysis Reveals a Strong Association of β‐Catenin With Cadherin Adherens Junctions in Resting Human Platelets. PROTEOMICS. 18(9). e1700419–e1700419. 9 indexed citations
2.
Ceria‐Ulep, Clementina D., John Grove, Randi Chen, et al.. (2010). Physical Aspects of Healthy Aging: Assessments of Three Measures of Balance for Studies in Middle-Aged and Older Adults. Current Gerontology and Geriatrics Research. 2010. 1–8. 11 indexed citations
3.
Curb, J. David, Clementina D. Ceria‐Ulep, Beatriz L. Rodríguez, et al.. (2006). Performance‐Based Measures of Physical Function for High‐Function Populations. Journal of the American Geriatrics Society. 54(5). 737–742. 178 indexed citations
4.
Kobori, J., et al.. (1999). Prader-Willi Syndrome Is Caused by Disruption of the SNRPN Gene. The American Journal of Human Genetics. 64(1). 70–76. 52 indexed citations
5.
Yancey, M K, et al.. (1996). Non‐mosaic trisomy 16 in a third‐trimester fetus. International Journal of Gynecology & Obstetrics. 55(2). 194–194. 20 indexed citations
6.
Malcolm, S & Tim Donlon. (1994). Report of the, Second International Workshop on Human Chromosome 15 Mapping 1994. Cytogenetic and Genome Research. 67(1). 1–22. 34 indexed citations
7.
Özçelık, Tayfun, Stuart E. Leff, Wendy P. Robinson, et al.. (1992). Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region. Nature Genetics. 2(4). 265–269. 214 indexed citations
8.
Comings, David E., Donn Muhleman, George Dietz, & Tim Donlon. (1991). Human tryptophan oxygenase localized to 4q31: Possible implications for alcoholism and other behavioral disorders. Genomics. 9(2). 301–308. 20 indexed citations
9.
Hsieh, Chih‐Lin, Tim Donlon, Basil T. Darras, et al.. (1990). The gene for the RNA component of the mitochondrial RNA-processing endoribonuclease is located on human chromosome 9p and on mouse chromosome 4. Genomics. 6(3). 540–544. 27 indexed citations
10.
Nagler, Arnon, et al.. (1990). Effects of recombinant human granulocyte colony stimulating factor and granulocyte-monocyte colony stimulating factor on in vitro hemopoiesis in the myelodysplastic syndromes.. PubMed. 4(3). 193–202. 29 indexed citations
11.
Donlon, Tim, et al.. (1990). Report of the committee on the genetic constitution of chromosome 15. Cytogenetic and Genome Research. 55(1-4). 189–193. 17 indexed citations
12.
Donlon, Tim. (1988). Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes. Human Genetics. 80(4). 322–328. 78 indexed citations
13.
Reeders, Stephen T. & Tim Donlon. (1988). Report on the genetic constitution of chromosome 16. Cytogenetic and Genome Research. 49(1-3). 94–94. 5 indexed citations
14.
Latt, S.A., Yosef Shiloh, G M Brodeur, et al.. (1986). Novel DNA rearrangement phenomena associated with DNA amplification in human neuroblastomas and neuroblastoma cell lines.. PubMed. 209A. 601–12. 2 indexed citations
15.
Shiloh, Yosef, Tim Donlon, G Bruns, Martin L. Breitman, & Lap‐Chee Tsui. (1986). Assignment of the human ?-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33?36. Human Genetics. 73(1). 17–19. 48 indexed citations
16.
Donlon, Tim, et al.. (1986). Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma.. PubMed. 23(2). 151–7. 18 indexed citations
17.
Müller, Ulrich, Marc Lalande, Tim Donlon, & Samuel A. Latt. (1986). Moderately repeated DNA sequences specific for the short arm of the human Y chromosome are present in XX males and reduced in copy number in an XY female. Nucleic Acids Research. 14(3). 1325–1340. 64 indexed citations
18.
Leonard, Warren J., Tim Donlon, Roger V. Lebo, & Warner C. Greene. (1985). Localization of the Gene Encoding the Human Interleukin-2 Receptor on Chromosome 10. Science. 228(4707). 1547–1549. 64 indexed citations
19.
Sakai, K, N Kanda, Yosef Shiloh, et al.. (1985). Molecular and cytologic analysis of DNA amplification in retinoblastoma. Cancer Genetics and Cytogenetics. 17(2). 95–112. 25 indexed citations
20.
Donlon, Tim, M. Litt, Samuel R. Newcom, & R.E. Magenis. (1983). Localization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization.. PubMed. 35(6). 1097–106. 36 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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