Jillian G. Buchan

2.8k citations

22 papers · 1.1k indexed · h-index 14

Developmental Biology top 5%
Cancer Research top 10%
- Cancer Genomics and Diagnostics 3
Genetics top 5%
- Genomics and Rare Diseases 6
- Connective tissue disorders research 5
- Neurogenetic and Muscular Disorders Research 3
- Genomic variations and chromosomal abnormalities 3
Genetics top 10%
- Genomics and Rare Diseases 6
- Connective tissue disorders research 5
- Neurogenetic and Muscular Disorders Research 3
- Genomic variations and chromosomal abnormalities 3
Molecular Biology
- Congenital heart defects research 3
- RNA modifications and cancer 3
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 5

Co-authors: Christina A. Gurnett Guangbo Liu Yong‐Yeon Cho Songnian Liu Feng Yang Fen Pei Lingxiao Li Amit Dipak Amin
Cited by: Developmental Biology Cancer Research Genetics
Journals: SHILAP Revista de lepidopterología (1 paper)Neurology (1 paper)Journal of Bone and Joint Surgery (2 papers)
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

The 25 scholars most cited alongside Jillian G. Buchan, 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 Jillian G. Buchan Line = papers co-authored together Jillian G. Buchan links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Looking beyond year 1 in the molecular era of pediatric brain tumor diagnosis: confirmatory testing of germline variants found on tumor sequencing Frontiers in Oncology ·Brittany L. Greene,Shannon M Stasi,Michelle Ting,Natalie Waligorski,Bonnie Cole,Christina M. Lockwood,Vera Paulson,Jillian G. Buchan,Amy S. Lee,Jeffrey G. Ojemann,Richard G. Ellenbogen,Jeffrey Stevens,Sarah Leary	2024	0
2	3-hour genome sequencing and targeted analysis to rapidly assess genetic risk SHILAP Revista de lepidopterología ·Miranda Pg Zalusky,Jonas A. Gustafson,Stephanie C. Bohaczuk,Benjamin J. Mallory,Paxton Reed,Tara Wenger,Erika Beckman,Irene J. Chang,Cate Paschal,Jillian G. Buchan,Christina M. Lockwood,Mihai Puia‐Dumitrescu,Daniel R. Garalde,Joseph Guillory,Androo J. Markham,Michael J. Bamshad,Evan E. Eichler,Andrew B. Stergachis,Danny E. Miller	2024	7
3	Effect of Uterine Leiomyomas on Noninvasive Prenatal Testing Parameters in the First Trimester Obstetrics and Gynecology ·Teodora Kolarova,Ali Alderson,Hayley J. MacKinnon,Leah Chen,Jillian G. Buchan,Christina M. Lockwood,Raj Shree	2024	0
4	Woodhouse–Sakati syndrome in an Indian patient with a novel pathogenic variant American Journal of Medical Genetics Part A ·S. Deepak Amalnath,Jothivanan,Junko Oshima,Jillian G. Buchan,Sarah Paolucci	2023	2
5	A Framework of Critical Considerations in Clinical Exome Reanalyses by Clinical and Laboratory Standards Institute Journal of Molecular Diagnostics ·Marco L. Leung,Jianling Ji,Samuel W. Baker,Jillian G. Buchan,Theru A. Sivakumaran,Bryan L. Krock,Rebecca L. Hutchins,Pınar Bayrak‐Toydemir,John D. Pfeifer,María Laura Cremona,Birgit Funke,Avni Santani	2022	4
6	Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease 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	2020	85
7	Rapid Genome Sequencing in the Critically Ill Clinical Chemistry ·Jillian G. Buchan,Shana White,Ruchi Joshi,Euan A. Ashley	2019	3
8	Canine MAS1: monoallelic expression is suggestive of an imprinted gene Animal Genetics ·Catherine M. Nolan,Robert E. Shiel,Jillian G. Buchan,Fiona O’Sullivan,John J. Callanan	2018	2
9	Long-read genome sequencing identifies causal structural variation in a Mendelian disease Genetics in Medicine ·Jason D. Merker,Aaron M. Wenger,Tam P. Sneddon,Megan E. Grove,Zachary Zappala,Laure Frésard,Daryl Waggott,Sowmi Utiramerur,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	2017	158
10	Are Copy Number Variants Associated With Adolescent Idiopathic Scoliosis? Clinical Orthopaedics and Related Research ·Jillian G. Buchan,David M. Alvarado,Gabe Haller,Hyuliya Aferol,Nancy H. Miller,Matthew B. Dobbs,Christina A. Gurnett	2014	13
11	Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis 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	2014	83
12	Kinesin family member 6 (kif6) is necessary for spine development in zebrafish Developmental Dynamics ·Jillian G. Buchan,Ryan S. Gray,John M. Gansner,David M. Alvarado,Lydia Burgert,Jonathan D. Gitlin,Christina A. Gurnett,Matthew Goldsmith	2014	56
13	MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposis Human Molecular Genetics ·Kyungsoo Ha,Jillian G. Buchan,David M. Alvarado,Kevin McCall,Anupama Vydyanath,Pradeep K. Luther,Matthew Goldsmith,Matthew B. Dobbs,Christina A. Gurnett	2013	47
14	Copy number analysis of 413 isolated talipes equinovarus patients suggests role for transcriptional regulators of early limb development European Journal of Human Genetics ·David M. Alvarado,Jillian G. Buchan,Steven L. Frick,John E. Herzenberg,Matthew B. Dobbs,Christina A. Gurnett	2012	32
15	Polygenic Threshold Model with Sex Dimorphism in Adolescent Idiopathic Scoliosis: The Carter Effect Journal of Bone and Joint Surgery ·Lisa M. Kruse,Jillian G. Buchan,Christina A. Gurnett,Matthew B. Dobbs	2012	30
16	Exome Sequencing Identifies an MYH3 Mutation in a Family with Distal Arthrogryposis Type 1 Journal of Bone and Joint Surgery ·David M. Alvarado,Jillian G. Buchan,Christina A. Gurnett,Matthew B. Dobbs	2011	31
17	Familial Isolated Clubfoot Is Associated with Recurrent Chromosome 17q23.1q23.2 Microduplications Containing TBX4 The American Journal of Human Genetics ·David M. Alvarado,Hyuliya Aferol,Kevin McCall,Jason B. Huang,Matthew Techy,Jillian G. Buchan,Janet Cady,Patrick R. Gonzales,Matthew B. Dobbs,Christina A. Gurnett	2010	61
18	Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy 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,K. Barnett,Martin R. Farlow,Judy Caress,G. Parry,Dianna Quan,Kathy Gardner,Ming Hong,Zachary Simmons,Thomas D. Bird,Phillip F. Chance,Mark Hannibal	2009	22
19	SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy Neurology ·Mark Hannibal,Elizabeth K. Ruzzo,Lauren Miller,Benjamin G Betz,Jillian G. Buchan,Dana Knutzen,K. Barnett,Megan Landsverk,Alexis Brice,Éric Leguern,H. Melanie Bedford,Bradford B. Worrall,S. Lovitt,Stanley H. Appel,E. Andermann,Thomas D. Bird,P. F. Chance	2009	40
20	Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high-performance liquid chromatography British Journal of Dermatology ·E.L. Rugg,John Common,Amanda L Wilgoss,Howard P. Stevens,Jillian G. Buchan,Irene M. Leigh,David P. Kelsell	2002	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), Prenatal Screening and Diagnostics (5 papers), Neurogenetic and Muscular Disorders Research (3 papers), Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), RNA modifications and cancer (3 papers) and Cancer Genomics and Diagnostics (3 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.

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