Gail E. Graham

3.6k total citations
60 papers, 1.9k citations indexed

About

Gail E. Graham is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Gail E. Graham has authored 60 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 21 papers in Genetics and 9 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Gail E. Graham's work include Neurogenetic and Muscular Disorders Research (5 papers), Genomics and Rare Diseases (4 papers) and Genetic Syndromes and Imprinting (4 papers). Gail E. Graham is often cited by papers focused on Neurogenetic and Muscular Disorders Research (5 papers), Genomics and Rare Diseases (4 papers) and Genetic Syndromes and Imprinting (4 papers). Gail E. Graham collaborates with scholars based in Canada, United States and United Kingdom. Gail E. Graham's co-authors include Kevin W. Garey, Margaret P. Price, Herbert L. DuPont, Errol B. Marliss, Charis Eng, Deborah J. Marsh, Roberto T. Zori, Martin J. Somerville, Susan E. Andrew and J. L. Steckley and has published in prestigious journals such as Nature Genetics, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Gail E. Graham

59 papers receiving 1.8k citations

Peers

Countries citing papers authored by Gail E. Graham

Since Specialization

Citations

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

Fields of papers citing papers by Gail E. Graham

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gail E. Graham. 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 Gail E. Graham. The network helps show where Gail E. Graham may publish in the future.

Co-authorship network of co-authors of Gail E. Graham

This figure shows the co-authorship network connecting the top 25 collaborators of Gail E. Graham. A scholar is included among the top collaborators of Gail E. Graham 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 Gail E. Graham. Gail E. Graham 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

#	Work	Indexed citations
1	“This Is Actually a Really Unique Moment in Time”: Navigating Long-Acting HIV Treatment and HIV Cure Research with Analytical Treatment Interruptions—A Qualitative Interview Study in the United States 2024 ·AIDS Research and Human Retroviruses ·Karine Dubé, Amaya Perez‐Brumer, Hursch Patel, (unknown), Lynda Dee, Gail E. Graham, Steven Meanley, Morgan M. Philbin	4
2	A partner protection package for HIV cure-related trials involving analytical treatment interruptions 2023 ·The Lancet Infectious Diseases ·Karine Dubé, (unknown), Lawrence Fox, Lynda Dee, David Palm, (unknown), (unknown), Jeff Taylor, Gail E. Graham, (unknown), John A. Sauceda, Michael J. Peluso, Annette Rid	13
3	Use of eConsult to enhance genetics service delivery in primary care: A multimethod study 2022 ·Genetics in Medicine ·June Carroll, Clare Liddy, Amir Afkham, (unknown), Elaine Goh, Gail E. Graham, Joanne Permaul, Judith Allanson, Ruth Heisey, (unknown), Donna Manca, Mary Ann O’Brien, Eva Grunfeld	5
4	Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition 2019 ·Genetics in Medicine ·Marta Unolt, Molka Kammoun, Beata Nowakowska, Gail E. Graham, T. Blaine Crowley, Matthew S. Hestand, (unknown), Maciej Geremek, Beverly S. Emanuel, Elaine H. Zackai, Joris Vermeesch, Donna M. McDonald‐McGinn	7
5	Application of Hereditary Renal Cell Carcinoma Risk Criteria to a Large Prospective Database 2019 ·Clinical Oncology ·Igal Kushnir, (unknown), Ranjeeta Mallick, Raymond H. Kim, Gail E. Graham, Rodney H. Breau, Jean‐Baptiste Lattouf, Philippe D. Violette, Stephen E. Pautler, Melanie Care, Anil Kapoor, Michael A.S. Jewett, Lori Wood, Simon Tanguay, D.Y.C. Heng, Naveen S. Basappa, Alan So, Frédéric Pouliot, Neil Reaume	5
6	A retrospective review of 48 individuals, including 12 families, molecularly diagnosed with hereditary leiomyomatosis and renal cell cancer (HLRCC) 2018 ·Familial Cancer ·(unknown), (unknown), Amanda Smith, Gail E. Graham	16
7	Severe craniosynostosis in an infant with deletion 22q11.2 syndrome 2012 ·American Journal of Medical Genetics Part A ·Walla Al‐Hertani, (unknown), Jean McGowan‐Jordan, (unknown), Gail E. Graham	3
8	Hyperekplexia: Treatment of a Severe Phenotype and Review of the Literature 2011 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Aleksandra Mineyko, Sharon Whiting, Gail E. Graham	11
9	Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13C 2011 ·American Journal of Medical Genetics Part A ·Karen W. Gripp, Elizabeth Hopkins, Katia Sol‐Church, Deborah L. Stabley, Marni E. Axelrad, Daniel Doyle, William B. Dobyns, Cindy Hudson, John P. Johnson, Romano Tenconi, Gail E. Graham, Ana Berta Sousa, Raoul Heller, Maria Piccione, Giovanni Corsello, Gail E. Herman, Marco Tartaglia, Angela E. Lin	48
10	Genetic education for primary care providers 2009 ·Canadian Family Physician ·June Carroll, Andrea L. Rideout, Brenda J. Wilson, (unknown), Sean Blaine, Mary Jane Esplen, Sandra A. Farrell, Gail E. Graham, Jennifer MacKenzie, Wendy S. Meschino, Fiona A. Miller, Preeti Prakash, Cheryl Shuman, Anne Summers, Sherry Taylor	6
11	Further clinical delineation of the Börjeson–Forssman–Lehmann syndrome in patients with PHF6 mutations 2009 ·American Journal of Medical Genetics Part A ·Melissa T. Carter, David J. Picketts, Alasdair G. W. Hunter, Gail E. Graham	23
12	Genotype-phenotype correlations in MYCN-related Feingold syndrome 2008 ·Human Mutation ·Carlo Marcelis, Frans A. Hol, Gail E. Graham, Paul N.M.A. Rieu, Richárd Kellermayer, Rowdy Meijer, Dorien Lugtenberg, Hans Scheffer, Hans van Bokhoven, Han G. Brunner, Arjan P.M. de Brouwer	60
13	Association of Interleukin-8 Polymorphism and Immunoglobulin G Anti–Toxin A in Patients With Clostridium difficile–Associated Diarrhea 2007 ·Clinical Gastroenterology and Hepatology ·(unknown), Kevin W. Garey, Margaret P. Price, Gail E. Graham, Pablo C. Okhuysen, (unknown), Mark LaRocco, Herbert L. DuPont	37
14	The Hunter–MacDonald syndrome with expanded phenotype including risk of meningioma: An update and review 2007 ·American Journal of Medical Genetics Part A ·Linlea Armstrong, Gail E. Graham, R. Neil Schimke, Debra L. Collins, Daniel J. Kirse, Fiona Costello, Holly H Ardinger	2
15	Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease 2006 ·Nature Genetics ·Mark I. Rees, Kirsten Harvey, Brian R. Pearce, Seo‐Kyung Chung, Ian Duguid, P K Thomas, (unknown), Gail E. Graham, Linlea Armstrong, Rita Shiang, (unknown), Sameer M. Zuberi, John B.P. Stephenson, Michael J. Owen, Marina A.J. Tijssen, Arn M. J. M. van den Maagdenberg, Trevor G. Smart, Stéphane Supplisson, Victoria L. Harvey	174
16	A Common Polymorphism in the Interleukin 8 Gene Promoter Is Associated with Clostridium difficile Diarrhea 2006 ·The American Journal of Gastroenterology ·Zhi‐Dong Jiang, Herbert L. DuPont, Kevin W. Garey, Margaret P. Price, Gail E. Graham, Pablo C. Okhuysen, (unknown), Mark LaRocco	69
17	High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome 2005 ·Human Mutation ·Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, Steffan Loff, Walter Back, Constanze Pagenstecher, D. Ross McLeod, Gail E. Graham, Elisabeth Mangold, René Santer, Peter Propping, Waltraut Friedl	174
18	Congenital Insensitivity to Pain with Anhidrosis: Novel Mutations in the TRKA (NTRK1) Gene Encoding A High-Affinity Receptor for Nerve Growth Factor 1999 ·The American Journal of Human Genetics ·(unknown), (unknown), Fumio Endo, Ichiro Matsuda, László Sztriha, Philippe Frossard, Allie Moosa, Essam A. R. Ismail, Alfons Macaya, Generoso Andria, (unknown), William T. Gibson, Gail E. Graham, (unknown)	121
19	Dyskeratosis congenita: An autosomal recessive variant 1999 ·American Journal of Medical Genetics ·Alison M. Elliott, Gail E. Graham, Mark L. Bernstein, Bruce Mazer, Ahmad S. Teebi	15
20	Congenital cholesteatoma and malformations of the facial nerve: Rare manifestations of the BOR syndrome 1999 ·American Journal of Medical Genetics ·Gail E. Graham, Judith Allanson	13

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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