Patrick MacLeod

5.5k citations

74 papers · 3.1k indexed · h-index 29

Impact in

Cellular and Molecular Neuroscience top 2%
- Genetic Neurodegenerative Diseases
Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research

Papers in ⓘ

Cellular and Molecular Neuroscience 25
- Genetic Neurodegenerative Diseases 20
Clinical Biochemistry 7
- Metabolism and Genetic Disorders 7

Co-authors: David G. Huntsman (3 shared papers)Carlos Caldas (3 shared papers)Raquel Seruca (3 shared papers)Charles E. Jackson (2 shared papers)J. Tapio Pantzar (2 shared papers)Barbara McGillivray (3 shared papers)Henry G. Dunn (3 shared papers)Kristin G. Monaghan (1 shared paper)
Journals: Neurology (5 papers)Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques (4 papers)Human Genetics (4 papers)Journal of the Neurological Sciences (4 papers)The Journal of Pediatrics (2 papers)
Partner nations: Canada United States Portugal

In The Last Decade

Patrick MacLeod

73 papers receiving 3.0k citations

Peers

Countries citing papers authored by Patrick MacLeod

Since Specialization

Citations

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

Fields of papers citing papers by Patrick MacLeod

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Patrick MacLeod, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Patrick MacLeod Line = papers co-authored together Patrick MacLeod links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 74 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Early Gastric Cancer in Young, Asymptomatic Carriers of Germ-Line E-Cadherin Mutations New England Journal of Medicine ·David G. Huntsman, Fátima Carneiro, Frank R. Lewis, Patrick MacLeod, Allen Hayashi, Kristin G. Monaghan, Raymond Maung, Raquel Seruca, Charles E. Jackson, Carlos Caldas	2001	281
2	Evidence for multi‐site closure of the neural tube in humans American Journal of Medical Genetics ·Margot I. Van Allen, Dagmar K. Kalousek, Gerold F. Chernoff, D. M. Juriloff, Muriel J. Harris, Barbara McGillivray, Siu‐Li Yong, Sylvie Langlois, Patrick MacLeod, David Chitayat, Jan M. Friedman, R.D. Wilson, Deborah E. McFadden, J. Tapio Pantzar, Susan Ritchie, Judith G. Hall	1993	280
3	Identification of germ-line E-cadherin mutations in gastric cancer families of European origin. PubMed ·Simon A. Gayther, Kylie L. Gorringe, Susan J. Ramus, David G. Huntsman, Giandomenico Roviello, Nicola Grehan, José Carlos Machado, Enrico Pinto, Raquel Seruca, Kevin C. Halling, Patrick MacLeod, Steven M. Powell, Charles E. Jackson, Bruce A.J. Ponder, Carlos Caldas	1998	245
4	Inherited Mutations in PTEN That Are Associated with Breast Cancer, Cowden Disease, and Juvenile Polyposis The American Journal of Human Genetics ·Eric D. Lynch, Elizabeth Ostermeyer, Ming K. Lee, J. Fernando Arena, Hanlee P. Ji, Jamie L. Dann, Karen Swisshelm, David Suchard, Patrick MacLeod, Stener Kvinnsland, Bjørn Tore Gjertsen, Ketil Heimdal, Herb Lubs, Pål Møller, Mary‐Claire King	1997	209
5	Predictive testing for Huntington disease in Canada: Adverse effects and unexpected results in those receiving a decreased risk American Journal of Medical Genetics ·Marlene J. Huggins, Maurice Bloch, Sandi Wiggins, Shelin Adam, Oksana Suchowersky, Michael Trew, Marylou Klimek, Cheryl R. Greenberg, Michael Eleff, Louise Thompson, Julie Knight, Patrick MacLeod, Kathleen Girard, Jane Theilmann, A Hedrick, Michael R. Hayden	1992	180
6	Mutations in the KIAA0196 Gene at the SPG8 Locus Cause Hereditary Spastic Paraplegia The American Journal of Human Genetics ·Paul N. Valdmanis, Inge A. Meijer, Annie Reynolds, Adrienne Lei, Patrick MacLeod, David Schlesinger, Mayana Zatz, Evan Reid, Patrick A. Dion, Pierre Drapeau, Guy A. Rouleau	2006	141
7	Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum Orphanet Journal of Rare Diseases ·Matthis Synofzik, Anne S. Soehn, Janina Gburek‐Augustat, Julia Schicks, Kathrin N. Karle, Rebecca Schüle, Tobias B. Haack, M. Schöning, Saskia Biskup, Sabine Rudnik‐Schöneborn, Jan Senderek, Karl‐Titus Hoffmann, Patrick MacLeod, Johannes Schwarz, Benjamin Bender, Stefan Krüger, Friedmar R. Kreuz, Peter Bauer, Lüdger Schöls	2013	125
8	Diagnosis and Management of Infantile Marfan Syndrome PEDIATRICS ·Richard P. Morse, Sol Rockenmacher, Reed E. Pyeritz, Stephen P. Sanders, Frederick R. Bieber, Angela E. Lin, Patrick MacLeod, Bryan D. Hall, John M. Graham	1990	123
9	Clinical and ultrastructural heterogeneity of type IV Ehlers-Danlos syndrome Human Genetics ·Peter H. Byers, Karen A. Holbrook, Barbara McGillivray, Patrick MacLeod, R. Brian Lowry	1979	96
10	Gas Exchange Abnormalities in Mild Bronchitis and Asymptomatic Asthma New England Journal of Medicine ·Gerald D. Levine, Filomena Housley, Patrick MacLeod, Peter T. Macklem	1970	84
11	Molecular characterization of L-CPT I deficiency in six patients: insights into function of the native enzyme Journal of Lipid Research ·Nicholas F. Brown, Rashmi Mullur, Indhu Subramanian, Victoria Esser, Michael J. Bennett, Jean‐Marie Saudubray, Annette S. Feigenbaum, Joyce A. Kobari, Patrick MacLeod, Julie McGarry, Jonathan C. Cohen	2001	83
12	Possible new autosomal recessive syndrome with unusual renal histopathological changes American Journal of Medical Genetics ·Judith Allanson, J. Tapio Pantzar, Patrick MacLeod	1983	76
13	Longevity in Rett Syndrome: Analysis of the North American Database The Journal of Pediatrics ·Russell S. Kirby, Jane B. Lane, Jerry Childers, Steve A. Skinner, Fran Annese, Judy O. Barrish, Daniel G. Glaze, Patrick MacLeod, Alan K. Percy	2009	73
14	Rett Syndrome: North American Database Journal of Child Neurology ·Alan K. Percy, Jane B. Lane, Jerry Childers, Steve A. Skinner, Fran Annese, Judy O. Barrish, Erwin Caeg, Daniel G. Glaze, Patrick MacLeod	2007	71
15	Rett Syndrome: Review of Biological Abnormalities Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Henry G. Dunn, Patrick MacLeod	2001	49
16	Cardiac malformations in the fetal alcohol syndrome The Journal of Pediatrics ·G Sándor, David F. Smith, Patrick MacLeod	1981	47
17	Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome. Journal of Medical Genetics ·Timothy Drumheller, Barbara McGillivray, D. Behrner, Patrick MacLeod, Deborah E. McFadden, J. Roberson, Charles P. Venditti, Karen Chorney, Michael J. Chorney, Jeremy C. Smith	1996	45
18	Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus. Journal of Medical Genetics ·Elspeth C. Twist, L K Casaubon, Martin Ruttledge, Vittal Rao, Patrick MacLeod, João Radvany, Zhen Zhao, Roger N. Rosenberg, Lindsay A. Farrer, Guy A. Rouleau	1995	44
19	Prenatal diagnosis of neuronal ceroid‐lipofuscinoses American Journal of Medical Genetics ·Patrick MacLeod, Clarissa L. Dolman, Robert E. Nickel, Eva Chang, Sukriti Nag, J. Zonana, Kerry Silvey, John M. Opitz, James F. Reynolds	1985	41
20	A familial factor independent of CAG repeat length influences age at onset of Machado-Joseph disease. PubMed ·Anita L. DeStefano, L. Adrienne Cupples, Patrı́cia Maciel, Cláudia Gaspar, João Radvany, D M Dawson, Lewis Sudarsky, L. A. Corwin, Paula Coutinho, Patrick MacLeod	1996	41

About Patrick MacLeod

Patrick MacLeod is a scholar working on Cellular and Molecular Neuroscience, Clinical Biochemistry, Neurology, Genetics and Rheumatology, having authored 74 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (20 papers), Mitochondrial Function and Pathology (13 papers), Genetics and Neurodevelopmental Disorders (9 papers), Lysosomal Storage Disorders Research (8 papers), Metabolism and Genetic Disorders (7 papers), DNA Repair Mechanisms (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Autism Spectrum Disorder Research (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (644 citations), Genetics (910 citations), Pathology and Forensic Medicine (411 citations), Pediatrics, Perinatology and Child Health (403 citations) and Molecular Biology (1.3k citations). Patrick MacLeod has collaborated with scholars based in Canada, United States and Portugal. Frequent co-authors include David G. Huntsman, Carlos Caldas, Raquel Seruca, Charles E. Jackson, J. Tapio Pantzar, Barbara McGillivray, Henry G. Dunn, Kristin G. Monaghan, Fátima Carneiro and Allen Hayashi. Their work appears in journals such as Neurology, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, Human Genetics, Journal of the Neurological Sciences and The Journal of Pediatrics.

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.

Explore authors with similar magnitude of impact