Jillian G. Buchan

2.8k citations

22 papers · 1.1k indexed · h-index 14

Co-authors: Christina A. Gurnett Guangbo Liu Yong‐Yeon Cho Songnian Liu Feng Yang Fen Pei Lingxiao Li Amit Dipak Amin
Topics: Genomics and Rare Diseases (6 papers)Connective tissue disorders research (5 papers)Prenatal Screening and Diagnostics (5 papers)
Cited by: Developmental Biology Cancer Research Genetics
Journals: SHILAP Revista de lepidopterologíaNeurology Journal of Bone and Joint Surgery
Partner nations: United States United Kingdom Canada

In The Last Decade

Jillian G. Buchan

20 papers receiving 1.0k citations

Peers

Countries citing papers authored by Jillian G. Buchan

Since Specialization

Citations

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

Fields of papers citing papers by Jillian G. Buchan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jillian G. Buchan. 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 Jillian G. Buchan. The network helps show where Jillian G. Buchan may publish in the future.

Co-authorship network of co-authors of Jillian G. Buchan

This figure shows the co-authorship network connecting the top 25 collaborators of Jillian G. Buchan. A scholar is included among the top collaborators of Jillian G. Buchan 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 Jillian G. Buchan. Jillian G. Buchan 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	Looking beyond year 1 in the molecular era of pediatric brain tumor diagnosis: confirmatory testing of germline variants found on tumor sequencing 2024 ·Frontiers in Oncology ·(unknown),(unknown),(unknown),(unknown),Bonnie Cole,Christina M. Lockwood,Vera Paulson,Jillian G. Buchan,Amy S. Lee,Jeffrey G. Ojemann,Richard G. Ellenbogen,Jeffrey Stevens,Sarah Leary	0
2	3-hour genome sequencing and targeted analysis to rapidly assess genetic risk 2024 ·SHILAP Revista de lepidopterología ·(unknown),(unknown),(unknown),Benjamin J. Mallory,(unknown),Tara Wenger,(unknown),Irene J. Chang,(unknown),Jillian G. Buchan,Christina M. Lockwood,Mihai Puia‐Dumitrescu,Daniel R. Garalde,(unknown),(unknown),Michael J. Bamshad,Evan E. Eichler,Andrew B. Stergachis,Danny E. Miller	7
3	Effect of Uterine Leiomyomas on Noninvasive Prenatal Testing Parameters in the First Trimester 2024 ·Obstetrics and Gynecology ·Teodora Kolarova,(unknown),(unknown),(unknown),Jillian G. Buchan,Christina M. Lockwood,Raj Shree	0
4	Woodhouse–Sakati syndrome in an Indian patient with a novel pathogenic variant 2023 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Junko Oshima,Jillian G. Buchan,(unknown)	2
5	A Framework of Critical Considerations in Clinical Exome Reanalyses by Clinical and Laboratory Standards Institute 2022 ·Journal of Molecular Diagnostics ·Marco L. Leung,Jianling Ji,Samuel W. Baker,Jillian G. Buchan,Theru A. Sivakumaran,Bryan L. Krock,(unknown),Pınar Bayrak‐Toydemir,John D. Pfeifer,María Laura Cremona,Birgit Funke,Avni Santani	4
6	Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease 2020 ·npj Genomic Medicine ·Christian R. Marshall,Shimul Chowdhury,Ryan J. Taft,Matthew S. Lebo,Jillian G. Buchan,Steven M. Harrison,Ross Rowsey,Eric W. Klee,Pengfei Liu,Elizabeth A. Worthey,Vaidehi Jobanputra,David Dimmock,Hutton M. Kearney,David Bick,Shashikant Kulkarni,Stacie L. Taylor,John W. Belmont,Dimitri J. Stavropoulos,Niall J. Lennon	85
7	Rapid Genome Sequencing in the Critically Ill 2019 ·Clinical Chemistry ·Jillian G. Buchan,Shana White,Ruchi Joshi,Euan A. Ashley	3
8	Canine MAS1: monoallelic expression is suggestive of an imprinted gene 2018 ·Animal Genetics ·Catherine M. Nolan,Robert E. Shiel,Jillian G. Buchan,Fiona O’Sullivan,John J. Callanan	2
9	Long-read genome sequencing identifies causal structural variation in a Mendelian disease 2017 ·Genetics in Medicine ·Jason D. Merker,Aaron M. Wenger,Tam P. Sneddon,Megan E. Grove,Zachary Zappala,Laure Frésard,Daryl Waggott,(unknown),Yanli Hou,Kevin S. Smith,Stephen B. Montgomery,Matthew T. Wheeler,Jillian G. Buchan,Christine Lambert,Kevin Eng,Luke Hickey,Jonas Korlach,James M. Ford,Euan A. Ashley	158
10	Are Copy Number Variants Associated With Adolescent Idiopathic Scoliosis? 2014 ·Clinical Orthopaedics and Related Research ·Jillian G. Buchan,David M. Alvarado,Gabe Haller,(unknown),Nancy H. Miller,Matthew B. Dobbs,Christina A. Gurnett	13
11	Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis 2014 ·Human Molecular Genetics ·Jillian G. Buchan,David M. Alvarado,Gabe Haller,Carlos Cruchaga,Matthew B. Harms,Tianxiao Zhang,Marcia Willing,Dorothy K. Grange,Alan C. Braverman,Nancy H. Miller,José A. Morcuende,Nelson L.S. Tang,Tsz Ping Lam,Bobby K. W. Ng,Jack C. Y. Cheng,Matthew B. Dobbs,Christina A. Gurnett	83
12	Kinesin family member 6 (kif6) is necessary for spine development in zebrafish 2014 ·Developmental Dynamics ·Jillian G. Buchan,Ryan S. Gray,John M. Gansner,David M. Alvarado,(unknown),Jonathan D. Gitlin,Christina A. Gurnett,Matthew Goldsmith	56
13	MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposis 2013 ·Human Molecular Genetics ·Kyungsoo Ha,Jillian G. Buchan,David M. Alvarado,Kevin McCall,(unknown),Pradeep K. Luther,Matthew Goldsmith,Matthew B. Dobbs,Christina A. Gurnett	47
14	Copy number analysis of 413 isolated talipes equinovarus patients suggests role for transcriptional regulators of early limb development 2012 ·European Journal of Human Genetics ·David M. Alvarado,Jillian G. Buchan,Steven L. Frick,John E. Herzenberg,Matthew B. Dobbs,Christina A. Gurnett	32
15	Polygenic Threshold Model with Sex Dimorphism in Adolescent Idiopathic Scoliosis: The Carter Effect 2012 ·Journal of Bone and Joint Surgery ·Lisa M. Kruse,Jillian G. Buchan,Christina A. Gurnett,Matthew B. Dobbs	30
16	Exome Sequencing Identifies an MYH3 Mutation in a Family with Distal Arthrogryposis Type 1 2011 ·Journal of Bone and Joint Surgery ·David M. Alvarado,Jillian G. Buchan,Christina A. Gurnett,Matthew B. Dobbs	31
17	Familial Isolated Clubfoot Is Associated with Recurrent Chromosome 17q23.1q23.2 Microduplications Containing TBX4 2010 ·The American Journal of Human Genetics ·David M. Alvarado,(unknown),Kevin McCall,(unknown),(unknown),Jillian G. Buchan,Janet Cady,Patrick R. Gonzales,Matthew B. Dobbs,Christina A. Gurnett	61
18	Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy 2009 ·Human Molecular Genetics ·Megan Landsverk,Elizabeth K. Ruzzo,Heather C. Mefford,Karen Buysse,Jillian G. Buchan,Evan E. Eichler,Elizabeth M. Petty,Esther A. Peterson,Dana Knutzen,(unknown),Martin R. Farlow,(unknown),G. Parry,Dianna Quan,Kathy Gardner,(unknown),Zachary Simmons,Thomas D. Bird,Phillip F. Chance,Mark Hannibal	22
19	SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy 2009 ·Neurology ·Mark Hannibal,Elizabeth K. Ruzzo,(unknown),(unknown),Jillian G. Buchan,Dana Knutzen,(unknown),Megan Landsverk,Alexis Brice,Éric Leguern,H. Melanie Bedford,Bradford B. Worrall,(unknown),Stanley H. Appel,E. Andermann,Thomas D. Bird,P. F. Chance	40
20	Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high-performance liquid chromatography 2002 ·British Journal of Dermatology ·E.L. Rugg,John Common,(unknown),Howard P. Stevens,Jillian G. Buchan,Irene M. Leigh,David P. Kelsell	10

About Jillian G. Buchan

Jillian G. Buchan is a scholar working on Developmental Biology, Genetics and Cancer Research, having authored 22 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Connective tissue disorders research (5 papers) and Prenatal Screening and Diagnostics (5 papers). The work is most often cited by research in Developmental Biology (40 citations), Cancer Research (203 citations) and Genetics (352 citations). Jillian G. Buchan has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Christina A. Gurnett, Guangbo Liu, Yong‐Yeon Cho, Songnian Liu, Feng Yang, Fen Pei, Lingxiao Li, Amit Dipak Amin, Matthew B. Dobbs and David M. Alvarado. Their work appears in journals such as SHILAP Revista de lepidopterología, Neurology and Journal of Bone and Joint Surgery.

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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