Kati J. Buckingham

6.6k citations

29 papers · 1.9k indexed · 1 hit paper · h-index 15

Co-authors: Michael J. Bamshad Jay Shendure Deborah A. Nickerson Abigail W. Bigham Sarah Ng Paul Shannon Karin M. Dent Chad D. Huff
Topics: Glycosylation and Glycoproteins Research (8 papers)HIV Research and Treatment (4 papers)Genomics and Rare Diseases (4 papers)
Cited by: Genetics Cancer Research Molecular Biology
Journals: Nature Genetics Blood PLoS ONE
Partner nations: United States Canada Kenya

In The Last Decade

Kati J. Buckingham

28 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Exome sequencing identifies the cause of a mendelian disorder

2009 1.3k citations Kati J. Buckingham, Abigail W. Bigham et al. profile →

Peers

Countries citing papers authored by Kati J. Buckingham

Since Specialization

Citations

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

Fields of papers citing papers by Kati J. Buckingham

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kati J. Buckingham. 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 Kati J. Buckingham. The network helps show where Kati J. Buckingham may publish in the future.

Co-authorship network of co-authors of Kati J. Buckingham

This figure shows the co-authorship network connecting the top 25 collaborators of Kati J. Buckingham. A scholar is included among the top collaborators of Kati J. Buckingham 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 Kati J. Buckingham. Kati J. Buckingham is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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

20 of 20 papers shown

#	Work	Indexed citations
1	The clinical utility of sequencing the entirety of CFTR 2024 ·Journal of Cystic Fibrosis ·Molly B. Sheridan,Melis A. Aksit,Kymberleigh A. Pagel,Kurt N. Hetrick,(unknown),(unknown),Kati J. Buckingham,Rhonda G. Pace,Hua Ling,Elizabeth Pugh,Wanda K. O’Neal,Michael J. Bamshad,Ronald L. Gibson,Michael R. Knowles,Scott M. Blackman,Garry R. Cutting,Karen S. Raraigh	1
2	Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects 2023 ·Human Genetics and Genomics Advances ·Jessica X. Chong,Matthew C. Childers,Colby T. Marvin,(unknown),Hernán Gonorazky,Lili‐Naz Hazrati,James J. Dowling,(unknown),Yasemin Alanay,Yolanda Ber,Miguel Ángel Marín Gabriel,Arthur S. Aylsworth,Kati J. Buckingham,Kathryn M. Shively,(unknown),(unknown),Michael Regnier,Michael J. Bamshad	9
3	Club cell secretory protein and lung function in children with cystic fibrosis 2022 ·Journal of Cystic Fibrosis ·Jing Zhai,Mary J. Emond,Amber Spangenberg,Debra A. Stern,Monica M. Vasquez,Elizabeth Blue,Kati J. Buckingham,Duane L. Sherrill,Marilyn Halonen,Ronald L. Gibson,Margaret Rosenfeld,Scott D. Sagel,Michael J. Bamshad,Wayne J. Morgan,Stefano Guerra	11
4	Inflammasome Genetic Variants, Macrophage Function, and Clinical Outcomes in Cystic Fibrosis 2021 ·American Journal of Respiratory Cell and Molecular Biology ·(unknown),William R. Berrington,Kati J. Buckingham,(unknown),(unknown),Margaret Rosenfeld,Michael J. Bamshad,Ronald L. Gibson,Thomas R. Hawn,Mary J. Emond	10
5	Mutations in the translocon‐associated protein complex subunit SSR3 cause a novel congenital disorder of glycosylation 2019 ·Journal of Inherited Metabolic Disease ·Bobby G. Ng,Charles Marques Lourenço,Marie‐Estelle Losfeld,Kati J. Buckingham,Martin Kircher,Deborah A. Nickerson,Jay Shendure,Michael J. Bamshad,Hudson H. Freeze	19
6	DPAGT1 Deficiency with Encephalopathy (DPAGT1-CDG): Clinical and Genetic Description of 11 New Patients 2018 ·JIMD Reports ·(unknown),Bobby G. Ng,Hunter R. Underhill,Lars Palm,Per Bengtson,Jean‐Michel Rozet,S. Gerber,Susanne Arnold,Xavier Zanlonghi,Cathy A. Stevens,Martin Kircher,Deborah A. Nickerson,Kati J. Buckingham,Kevin D. Josephson,Jay Shendure,Michael J. Bamshad,Hudson H. Freeze,Erik A. Eklund	15
7	Encephalopathy caused by novel mutations in the CMP‐sialic acid transporter, SLC35A1 2017 ·American Journal of Medical Genetics Part A ·Bobby G. Ng,Carla Asteggiano,Martin Kircher,Kati J. Buckingham,Kimiyo Raymond,Deborah A. Nickerson,Jay Shendure,Michael J. Bamshad,(unknown),Hudson H. Freeze	26
8	Whole genome sequencing of extreme phenotypes identifies variants in CD101 and UBE2V1 associated with increased risk of sexually acquired HIV-1 2017 ·PLoS Pathogens ·Romel D. Mackelprang,Michael J. Bamshad,Jessica X. Chong,(unknown),Kati J. Buckingham,Kathryn M. Shively,Guy de Bruyn,Nelly Mugo,James I. Mullins,M. Juliana McElrath,Jared M. Baeten,Connie Celum,Mary J. Emond,Jairam R. Lingappa,(unknown)	11
9	Activation of a cryptic splice site in the mitochondrial elongation factor GFM1 causes combined OXPHOS deficiency 2017 ·Mitochondrion ·Mariella Simon,Bobby G. Ng,Marisa W. Friederich,Raymond Wang,Monica Boyer,Martin Kircher,Renata Collard,Kati J. Buckingham,Richard Chang,Jay Shendure,Deborah A. Nickerson,Michael J. Bamshad,Johan L.K. Van Hove,Hudson H. Freeze,José E. Abdenur	17
10	SRD5A3‐CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features 2016 ·American Journal of Medical Genetics Part A ·Patricia G. Wheeler,Bobby G. Ng,(unknown),V. Reid Sutton,Dennis W. Bartholomew,Matthew Pastore,Michael J. Bamshad,Martin Kircher,Kati J. Buckingham,Deborah A. Nickerson,Jay Shendure,Hudson H. Freeze	25
11	Expanding the Molecular and Clinical Phenotype of SSR4-CDG 2015 ·Human Mutation ·Bobby G. Ng,Kimiyo Raymond,Martin Kircher,Kati J. Buckingham,Tim Wood,Jay Shendure,Deborah A. Nickerson,Michael J. Bamshad,(unknown),Fabíola Paoli Monteiro,Brett H. Graham,(unknown),Rebecca Sparkes,Angela E. Scheuerle,Sara Cathey,Fernando Kok,James B. Gibson,Hudson H. Freeze	25
12	Variants in Host Viral Replication Cycle Genes Are Associated With Heterosexual HIV-1 Acquisition in Africans 2014 ·JAIDS Journal of Acquired Immune Deficiency Syndromes ·Abigail W. Bigham,Romel D. Mackelprang,Connie Celum,Guy de Bruyn,Kristin Beima‐Sofie,Grace John‐Stewart,Allan Ronald,Nelly Mugo,Kati J. Buckingham,Michael J. Bamshad,James I. Mullins,M. Juliana McElrath,Jairam R. Lingappa	5
13	TCIRG1-Associated Congenital Neutropenia 2014 ·Human Mutation ·Vahagn Makaryan,Elisabeth A. Rosenthal,Audrey Anna Bolyard,Merideth L. Kelley,Jennifer E. Below,Michael J. Bamshad,(unknown),Joshua D. Smith,Kati J. Buckingham,Laurence A. Boxer,Julia Skokowa,Karl Welte,Deborah A. Nickerson,Gail P. Jarvik,David C. Dale	30
14	Multiple mutant T alleles cause haploinsufficiency of Brachyury and short tails in Manx cats 2013 ·Mammalian Genome ·Kati J. Buckingham,Margaret J. McMillin,Margaret M. Brassil,Kathryn M. Shively,Kevin M. Magnaye,(unknown),Amy S. Weinmann,Leslie A. Lyons,Michael J. Bamshad	37
15	Toll-like Receptor Polymorphism Associations With HIV-1 Outcomes Among Sub-Saharan Africans 2013 ·The Journal of Infectious Diseases ·Romel D. Mackelprang,Abigail W. Bigham,Connie Celum,Guy de Bruyn,Kristin Beima‐Sofie,Grace John‐Stewart,Allan Ronald,Nelly Mugo,Kati J. Buckingham,Michael J. Bamshad,James I. Mullins,M. Juliana McElrath,Jairam R. Lingappa	28
16	TCIRG1 Associated Congenital Neutropenia 2013 ·Blood ·Vahagn Makaryan,Elisabeth A. Rosenthal,Audrey Anna Bolyard,Merideth L. Kelley,Jennifer E. Below,Michael J. Bamshad,(unknown),Joshua D. Smith,Kati J. Buckingham,Laurence A. Boxer,Julia Skokowa,Karl Welte,Deborah A. Nickerson,Gail P. Jarvik,David C. Dale	1
17	A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex 2013 ·Human Molecular Genetics ·Marie‐Estelle Losfeld,Bobby G. Ng,Martin Kircher,Kati J. Buckingham,Emily H. Turner,Alexey M. Eroshkin,Joshua D. Smith,Jay Shendure,D. A. Nickerson,Michael J. Bamshad,Hudson H. Freeze	52
18	Host Genetic Risk Factors for West Nile Virus Infection and Disease Progression 2011 ·PLoS ONE ·Abigail W. Bigham,Kati J. Buckingham,(unknown),Mary J. Emond,(unknown),Heidi Gildersleeve,Ann Rutherford,(unknown),Andrey A. Perelygin,Michael P. Busch,Kristy O. Murray,James J. Sejvar,Sharone Green,John D. Kriesel,Margo A. Brinton,Michael J. Bamshad	97
19	Cryptic gametic interactions confer both conspecific and heterospecific advantages in the Chrysochus (Coleoptera: Chrysomelidae) hybrid zone 2011 ·Genetica ·Merrill A. Peterson,Erica L. Larson,Margaret M. Brassil,Kati J. Buckingham,(unknown),(unknown),(unknown),Michael A. White,(unknown),(unknown),Kirsten J. Monsen	7
20	RELATIVE ABUNDANCE AND THE SPECIES-SPECIFIC REINFORCEMENT OF MALE MATING PREFERENCE IN THE CHRYSOCHUS (COLEOPTERA: CHRYSOMELIDAE) HYBRID ZONE 2005 ·Evolution ·Merrill A. Peterson,Barbara M. Honchak,(unknown),(unknown),(unknown),(unknown),Kati J. Buckingham,Michael A. White,Kirsten J. Monsen	5

About Kati J. Buckingham

Kati J. Buckingham is a scholar working on Virology, Immunology and Genetics, having authored 29 papers that have together received 1.9k indexed citations. Recurring topics across this work include Glycosylation and Glycoproteins Research (8 papers), HIV Research and Treatment (4 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (951 citations), Cancer Research (234 citations) and Molecular Biology (999 citations). Kati J. Buckingham has collaborated with scholars based in United States, Canada and Kenya. Frequent co-authors include Michael J. Bamshad, Jay Shendure, Deborah A. Nickerson, Abigail W. Bigham, Sarah Ng, Paul Shannon, Karin M. Dent, Chad D. Huff, Ethylin Wang Jabs and Choli Lee. Their work appears in journals such as Nature Genetics, Blood and PLoS ONE.

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