P.M. Conneally

5.7k total citations
63 papers, 3.4k citations indexed

About

P.M. Conneally is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, P.M. Conneally has authored 63 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 23 papers in Cellular and Molecular Neuroscience and 21 papers in Genetics. Recurrent topics in P.M. Conneally's work include Genetic Neurodegenerative Diseases (21 papers), Alzheimer's disease research and treatments (11 papers) and Mitochondrial Function and Pathology (6 papers). P.M. Conneally is often cited by papers focused on Genetic Neurodegenerative Diseases (21 papers), Alzheimer's disease research and treatments (11 papers) and Mitochondrial Function and Pathology (6 papers). P.M. Conneally collaborates with scholars based in United States, United Kingdom and Italy. P.M. Conneally's co-authors include Lindsay A. Farrer, J. Ott, M. E. Hodes, Tatiana M. Foroud, R.M. Ridley, Chris Frith, James F. Gusella, Jonathan L. Haines, Jacqueline S. Gray and N.E. Morton and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

P.M. Conneally

61 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P.M. Conneally United States 33 1.9k 1.0k 993 538 487 63 3.4k
P. Michael Conneally United States 38 3.0k 1.6× 1.4k 1.4× 2.7k 2.8× 658 1.2× 1.8k 3.7× 66 6.2k
Philippe Brachet France 31 1.1k 0.6× 319 0.3× 908 0.9× 379 0.7× 226 0.5× 76 3.1k
P. M. Conneally United States 26 1.8k 0.9× 659 0.6× 760 0.8× 1.5k 2.7× 515 1.1× 61 3.9k
Matthias Vorgerd Germany 41 3.1k 1.6× 359 0.3× 1.4k 1.4× 684 1.3× 686 1.4× 183 5.1k
Teresa L. Wood United States 44 2.5k 1.3× 798 0.8× 657 0.7× 404 0.8× 185 0.4× 113 5.1k
James K. Pretorius United States 29 1.7k 0.9× 337 0.3× 2.9k 3.0× 302 0.6× 248 0.5× 38 4.7k
Margaret A. Pericak‐Vance United States 34 2.2k 1.2× 928 0.9× 1.6k 1.6× 1.1k 2.1× 650 1.3× 71 5.2k
David G. Wells United States 26 1.8k 0.9× 328 0.3× 1.2k 1.2× 306 0.6× 138 0.3× 59 3.3k
Yoshigoro Kuroiwa Japan 36 1.5k 0.8× 218 0.2× 891 0.9× 605 1.1× 1.7k 3.4× 211 4.6k
O. Robain France 31 1.6k 0.9× 337 0.3× 994 1.0× 295 0.5× 234 0.5× 86 3.2k

Countries citing papers authored by P.M. Conneally

Since Specialization
Citations

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

Fields of papers citing papers by P.M. Conneally

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P.M. Conneally. 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 P.M. Conneally. The network helps show where P.M. Conneally may publish in the future.

Co-authorship network of co-authors of P.M. Conneally

This figure shows the co-authorship network connecting the top 25 collaborators of P.M. Conneally. A scholar is included among the top collaborators of P.M. Conneally 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 P.M. Conneally. P.M. Conneally 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.
Martin, Eden R., John R. Gilbert, Eric Lai, et al.. (2000). Analysis of Association at Single Nucleotide Polymorphisms in the APOE Region. Genomics. 63(1). 7–12. 47 indexed citations
2.
Vance, Jeffery M., Janet M. Grubber, Lisa Bailey, et al.. (2000). Identification of Novel Genes in Late-Onset Alzheimer's Disease. Experimental Gerontology. 35(9-10). 1343–1352. 153 indexed citations
3.
Scott, William K., Janet M. Grubber, P.M. Conneally, et al.. (2000). Fine Mapping of the Chromosome 12 Late-Onset Alzheimer Disease Locus: Potential Genetic and Phenotypic Heterogeneity. The American Journal of Human Genetics. 66(3). 922–932. 82 indexed citations
4.
Grubber, Janet M., Ann M. Saunders, William K. Scott, et al.. (1999). Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K). Neuroscience Letters. 269(2). 115–119. 32 indexed citations
5.
Foroud, Tatiana M., et al.. (1999). Differences in duration of Huntington's disease based on age at onset. Journal of Neurology Neurosurgery & Psychiatry. 66(1). 52–56. 158 indexed citations
6.
Begleiter, Henri, Theodore Reich, John I. Nürnberger, et al.. (1999). Description of the genetic analysis workshop 11 collaborative study on the genetics of alcoholism. Genetic Epidemiology. 17(S1). S25–30. 39 indexed citations
7.
Vance, Jeffery M., Larry H. Yamaoka, P. C. Gaskell, et al.. (1998). Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease. Neurobiology of Aging. 19(1). S39–S42. 44 indexed citations
8.
Scott, William K., Larry H. Yamaoka, P. A. Locke, et al.. (1997). No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease. Genetic Epidemiology. 14(3). 307–315. 28 indexed citations
9.
Small, Gary W., Ernest P. Noble, Steven S. Matsuyama, et al.. (1997). D2 Dopamine Receptor A1 Allele in Alzheimer Disease and Aging. Archives of Neurology. 54(3). 281–285. 10 indexed citations
10.
Quaid, Kimberly A., et al.. (1996). Issues in Genetic Testing for Susceptibility to Alcoholism: Lessons from Alzheimer's Disease and Huntington's Disease. Alcoholism Clinical and Experimental Research. 20(8). 1430–1437. 13 indexed citations
11.
Locke, P. A., P.M. Conneally, Rudolph E. Tanzi, James F. Gusella, & Jonathan L. Haines. (1995). Apolipoprotein E4 allele and Alzheimer disease: Examination of Allelic association and effect on age at onset in both early‐and late‐onset cases. Genetic Epidemiology. 12(1). 83–92. 62 indexed citations
12.
Young, Keith A., Tatiana Foroud, Paul Williams, et al.. (1992). Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15. Genomics. 13(4). 1370–1371. 31 indexed citations
13.
Haines, Jonathan L., James A. Trofatter, Rudolph E. Tanzi, et al.. (1992). Chromosome 21 genetic linkage data set based on the Venezuelan reference pedigree. Cytogenetic and Genome Research. 59(2-3). 88–89. 1 indexed citations
14.
Pratt, Victoria M., et al.. (1991). A new mutation in the proteolipid protein (PLP) gene in a German family with pelizaeus‐merzbacher disease. American Journal of Medical Genetics. 38(1). 136–139. 36 indexed citations
15.
Sadovnick, A. Dessa, Marleen Irwin, Patricia A. Baird, B. Lynn Beattie, & P.M. Conneally. (1989). Genetic studies on an Alzheimer Clinic population. Genetic Epidemiology. 6(5). 633–643. 21 indexed citations
16.
Haines, J. L., Laurie J. Ozelius, Peter St George‐Hyslop, et al.. (1988). Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes. Genetic Epidemiology. 5(6). 375–380. 9 indexed citations
17.
Pericak‐Vance, Margaret A., P.M. Conneally, A.D. Merritt, et al.. (1978). Genetic linkage studies in Huntington disease. Cytogenetic and Genome Research. 22(1-6). 640–645. 15 indexed citations
18.
Conneally, P.M., et al.. (1976). Linkage Relations of the Loci for Kell and Phenylthiocarbamide Taste Sensitivity. Human Heredity. 26(4). 267–271. 27 indexed citations
19.
Conneally, P.M., E.W. Lovrien, R.E. Magenis, et al.. (1976). The linkage and mapping relationships of 1qh. Cytogenetic and Genome Research. 16(1-5). 347–350. 4 indexed citations
20.
Meyers, Deborah A., P.M. Conneally, E.W. Lovrien, et al.. (1976). Linkage group I: the simultaneous estimation of recombination and interference. Cytogenetic and Genome Research. 16(1-5). 335–339. 13 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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