Ian M. Campbell

4.5k citations

81 papers · 1.8k indexed · h-index 23

Co-authors: Chad A. Shaw James R. Lupski Christopher N Gray Paweł Stankiewicz Robert Mason Christine R. Beck Grzegorz Ira B. A. Thrush
Topics: Genomic variations and chromosomal abnormalities (15 papers)Genomics and Rare Diseases (12 papers)Congenital heart defects research (6 papers)
Cited by: Genetics Atmospheric Science Molecular Biology
Journals: Nature Science Nucleic Acids Research
Partner nations: United States United Kingdom Canada

In The Last Decade

Ian M. Campbell

78 papers receiving 1.7k citations

Peers

Countries citing papers authored by Ian M. Campbell

Since Specialization

Citations

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

Fields of papers citing papers by Ian M. Campbell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ian M. Campbell

This figure shows the co-authorship network connecting the top 25 collaborators of Ian M. Campbell. A scholar is included among the top collaborators of Ian M. Campbell 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 Ian M. Campbell. Ian M. Campbell 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	Phenotype driven molecular genetic test recommendation for diagnosing pediatric rare disorders 2024 ·npj Digital Medicine ·(unknown),Priyanka Ahimaz,Nga Nguyen,Rachel Lewis,Wendy K. Chung,Casey Ta,(unknown),Sarah E. Sheppard,Ian M. Campbell,Kai Wang,Chunhua Weng,Cong Liu	2
2	Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression 2022 ·Clinical Genetics ·Ian M. Campbell,T. Blaine Crowley,Chintan Jobaliya,Alice Bailey,Daniel E. McGinn,(unknown),Anne S. Bassett,Raquel E. Gur,Bernice E. Morrow,Beverly S. Emanuel,Aime T. Franco,Deborah L. French,Elaine H. Zackai,Donna M. McDonald‐McGinn,Michele P. Lambert	4
3	Metabolomic profiling of samples from pediatric patients with asthma unveils deficient nutrients in African Americans 2022 ·iScience ·Hui‐Qi Qu,Joseph Glessner,(unknown),(unknown),Frank Mentch,Ian M. Campbell,Patrick Sleiman,John J. Connolly,Håkon Håkonarson	8
4	Metabolomic profiling for dyslipidemia in pediatric patients with sickle cell disease, on behalf of the IHCC consortium 2022 ·Metabolomics ·Hui‐Qi Qu,Joseph Glessner,(unknown),Frank Mentch,Ian M. Campbell,Patrick Sleiman,John J. Connolly,Håkon Håkonarson	4
5	Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature 2022 ·Molecular Genetics and Metabolism Reports ·Jessica Priestley,(unknown),(unknown),Anjali Aggarwal,Cesar Alves,Ian M. Campbell,(unknown),(unknown),(unknown),(unknown),Andrea Gropman,Ingo Helbig,Xinying Hong,(unknown),(unknown),Pamela Trapane,Varunvenkat M. Srinivasan,Pim Suwannarat,Rebecca Ganetzky	10
6	Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDH 2021 ·Journal of Medical Genetics ·(unknown),Ian M. Campbell,Andrés Hernández,Seema R. Lalani,Pengfei Liu,Chad A. Shaw,Jill A. Rosenfeld,Daryl A. Scott	21
7	Proposed criteria for nevoid basal cell carcinoma syndrome in children assessed using statistical optimization 2021 ·Scientific Reports ·Nina B. Gold,Ian M. Campbell,Sarah E. Sheppard,Wen‐Hann Tan	5
8	Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases 2021 ·Journal of Allergy and Clinical Immunology ·T. Blaine Crowley,Ian M. Campbell,Emily J. Liebling,Michele P. Lambert,Lorraine E. Levitt Katz,Jennifer Heimall,Alice Bailey,Daniel E. McGinn,Donna M. McDonald‐McGinn,Kathleen E. Sullivan	16
9	Vertical transmission of a large calvarial ossification defect due to heterozygous variants of ALX4 and TWIST1 2020 ·American Journal of Medical Genetics Part A ·(unknown),Yves Lacassie,Mahshid S. Azamian,(unknown),Gladys Zapata,Patricia Hernandez,Pengfei Liu,Ian M. Campbell,Bret L. Bostwick,Seema R. Lalani	1
10	Field Survey in the Basentello Valley on the Basilicata-Puglia Border 2018 ·Project Muse (Johns Hopkins University) ·Alastair Small,(unknown),Ian M. Campbell,(unknown),Tracy Prowse,(unknown)	2
11	Predicting human genes susceptible to genomic instability associated with Alu/Alu-mediated rearrangements 2018 ·Genome Research ·Xiaofei Song,Christine R. Beck,Renqian Du,Ian M. Campbell,Zeynep Coban‐Akdemir,Shen Gu,Amy M. Breman,Paweł Stankiewicz,Grzegorz Ira,Chad A. Shaw,James R. Lupski	51
12	Somatic mosaicism: implications for disease and transmission genetics 2015 ·Trends in Genetics ·Ian M. Campbell,Chad A. Shaw,Paweł Stankiewicz,James R. Lupski	179
13	Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles 2013 ·Genome Research ·Philip M. Boone,Ian M. Campbell,(unknown),Zachry T. Soens,(unknown),Patricia Hixson,Ankita Patel,Weimin Bi,Sau Wai Cheung,Seema R. Lalani,Arthur L. Beaudet,Paweł Stankiewicz,Chad A. Shaw,James R. Lupski	45
14	Mutations inVRK1Associated With Complex Motor and Sensory Axonal Neuropathy Plus Microcephaly 2013 ·JAMA Neurology ·Claudia Gonzaga‐Jauregui,Timothy Lotze,Leila Jamal,Samantha Penney,Ian M. Campbell,Davut Pehli̇van,Jill V. Hunter,(unknown),Gerald V. Raymond,Adekunle M. Adesina,Shalini N. Jhangiani,Jeffrey G. Reid,Donna M. Muzny,Eric Boerwinkle,James R. Lupski,Richard A. Gibbs,Wojciech Wiszniewski	41
15	Incidental copy-number variants identified by routine genome testing in a clinical population 2012 ·Genetics in Medicine ·Philip M. Boone,Zachry T. Soens,Ian M. Campbell,Paweł Stankiewicz,Sau Wai Cheung,Ankita Patel,Arthur L. Beaudet,Sharon E. Plon,Chad A. Shaw,Amy L. McGuire,James R. Lupski	30
16	TGFBR2 deletion in a 20‐month‐old female with developmental delay and microcephaly 2011 ·American Journal of Medical Genetics Part A ·Ian M. Campbell,Katarzyna Kołodziejska,Michael Quach,(unknown),Sau Wai Cheung,Seema R. Lalani,Melissa B. Ramocki,Paweł Stankiewicz	13
17	The distribution of Mekong schistosomiasis, past and future: Preliminary indications from an analysis of genetic variation in the intermediate host 2008 ·Parasitology International ·Stephen W. Attwood,Farrah A. Fatih,Ian M. Campbell,E. S. Upatham	31
18	In Vitro Comparative Kinetic Analysis of the Chloroplast Toc GTPases 2007 ·Journal of Biological Chemistry ·L. Evan Reddick,Michael Vaughn,Sarah J Wright,Ian M. Campbell,Barry D. Bruce	37
19	Tuberculosis control and medical schools : report of a WHO workshop, Rome, Italy, 29-31 October, 1997 1998 ·World Health Organization eBooks ·P Chaulet,Ian M. Campbell,Charles Boelen	2
20	A Prospective Study of Factors Influencing HIV Infection in Homosexual and Bisexual Men: Interim Report of Findings to Stage II 1990 ·Ian M. Campbell,(unknown),(unknown),C. R. Lucas	1

About Ian M. Campbell

Ian M. Campbell is a scholar working on Genetics, Insect Science and Molecular Biology, having authored 81 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Genomics and Rare Diseases (12 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Genetics (568 citations), Atmospheric Science (236 citations) and Molecular Biology (730 citations). Ian M. Campbell has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Chad A. Shaw, James R. Lupski, Christopher N Gray, Paweł Stankiewicz, Robert Mason, Christine R. Beck, Grzegorz Ira, B. A. Thrush, Marenda A. Wilson and Yang Yu. Their work appears in journals such as Nature, Science and Nucleic Acids Research.

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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