Eden Haverfield

2.8k citations

23 papers · 536 indexed · h-index 13

Genetics top 10%
Molecular Biology
Pediatrics, Perinatology and Child Health top 10%
Genetics
Cancer Research

Co-authors: Ryk Ward Nourdine Bouzekri Soma Das Kristin Petras William B. Dobyns Sean Myles Jean‐Michel Dugoujon Mohamed Cherkaoui
Topics: BRCA gene mutations in cancer (5 papers)Genomics and Rare Diseases (4 papers)Genomic variations and chromosomal abnormalities (4 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health
Journals: Blood Cancer Research Fertility and Sterility
Partner nations: United States United Kingdom Germany

In The Last Decade

Eden Haverfield

22 papers receiving 517 citations

Peers

Countries citing papers authored by Eden Haverfield

Since Specialization

Citations

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

Fields of papers citing papers by Eden Haverfield

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eden Haverfield. 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 Eden Haverfield. The network helps show where Eden Haverfield may publish in the future.

Co-authorship network of co-authors of Eden Haverfield

This figure shows the co-authorship network connecting the top 25 collaborators of Eden Haverfield. A scholar is included among the top collaborators of Eden Haverfield 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 Eden Haverfield. Eden Haverfield 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 Impact of Proband Indication for Genetic Testing on the Uptake of Cascade Testing Among Relatives 2022 ·Frontiers in Genetics ·Tara Schmidlen,Sara L. Bristow,Kathryn E. Hatchell,Edward D. Esplin,Robert L. Nussbaum,Eden Haverfield	21
2	Limited-Variant Screening vs Comprehensive Genetic Testing for Familial Hypercholesterolemia Diagnosis 2021 ·JAMA Cardiology ·Amy C. Sturm,Rebecca Truty,Thomas E. Callis,(unknown),Edward D. Esplin,(unknown),Eden Haverfield,Ana Morales,Robert L. Nussbaum,Susan Rojahn,Matteo Vatta,Daniel J. Rader	18
3	GENETIC SCREENING IN REPRODUCTIVE AGE WOMEN IDENTIFIES A HIGH POSITIVE RATE OF ACTIONABLE RESULTS 2020 ·Fertility and Sterility ·(unknown),Eden Haverfield,Edward D. Esplin,Robert L. Nussbaum,Swaroop Aradhya	0
4	Abstract P4-03-06: Limitations of direct-to-consumer genetic screening for HBOC: False negatives, false positives and everything in between 2019 ·Cancer Research ·Edward D. Esplin,Eden Haverfield,Shan Yang,Blanca Herrera,Michael J. Anderson,(unknown)	4
5	Cleft palate and hypopituitarism in a patient with Noonan‐like syndrome with loose anagen hair‐1 2018 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Marsha L. Davenport,Eden Haverfield,Maheer M. Masood,(unknown),Arthur S. Aylsworth	9
6	Clinical Genetic Testing for the Cardiomyopathies and Arrhythmias: A Systematic Framework for Establishing Clinical Validity and Addressing Genotypic and Phenotypic Heterogeneity 2016 ·Frontiers in Cardiovascular Medicine ·John Garcia,Jackie Tahiliani,(unknown),(unknown),(unknown),Amy Daly,(unknown),Eden Haverfield,Blanca Herrera,Laura Murillo,Keith Nykamp,Scott Topper	19
7	Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder 2016 ·American Journal of Medical Genetics Part A ·Francisca Millan,Megan T. Cho,Kyle Retterer,Kristin G. Monaghan,Renkui Bai,Patrik Vitazka,David B. Everman,Brooke Smith,Brad Angle,Victoria H. J. Roberts,LaDonna Immken,(unknown),Marc DiFazio,Elliott H. Sherr,Eden Haverfield,Bethany Friedman,Aida Telegrafi,Jane Juusola,Wendy K. Chung,Sherri J. Bale	42
8	FTO variant associated with malformation syndrome 2015 ·American Journal of Medical Genetics Part A ·Luis Rohena,(unknown),Edwin R. Guzman,Mythily Ganapathi,Megan T. Cho,Eden Haverfield,Kwame Anyane‐Yeboa	14
9	Whole-Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death 2015 ·Pediatric and Developmental Pathology ·(unknown),Eden Haverfield,Wendy K. Chung	7
10	Loss of function mutation in glutamic pyruvate transaminase 2 (GPT2) causes developmental encephalopathy 2015 ·Journal of Inherited Metabolic Disease ·Katrina Celis,(unknown),Eden Haverfield,Joshua Cappell,Rongze Yang,Da‐Wei Gong,Wendy K. Chung	20
11	Nonspecific phenotype of Noonan syndrome diagnosed by whole exome sequencing 2015 ·Clinical Case Reports ·(unknown),Julia Wynn,Eden Haverfield,Wendy K. Chung	3
12	Assessing copy number from exome sequencing and exome array CGH based on CNV spectrum in a large clinical cohort 2014 ·Genetics in Medicine ·Kyle Retterer,Julie Scuffins,Daniel Schmidt,Rachel Lewis,Daniel Pineda‐Alvarez,Amanda Stafford,Lindsay Schmidt,(unknown),Federica Gibellini,(unknown),A. D. Blair,Sherri J. Bale,Ludmila Matyakhina,Jeanne Meck,Swaroop Aradhya,Eden Haverfield	86
13	Molecular confirmation of nine cases of Cornelia de Lange syndrome diagnosed prenatally 2013 ·Prenatal Diagnosis ·Melissa A Dempsey,Anthony E. Johnson,(unknown),Julie S. Moldenhauer,(unknown),Karen Chong,David Chitayat,Lauren C. Briere,Helen N. Lyon,(unknown),Sameer Vali Gopalani,Joseph R. Siebert,Sébastien Lévesque,J LEBLANC,Donald Menzies,Eden Haverfield,Soma Das	8
14	A pharmacogenetic study of vorinostat glucuronidation 2010 ·Pharmacogenetics and Genomics ·Soonmo Peter Kang,Jacqueline Ramı́rez,Larry House,Wei Zhang,Snezana Mirkov,Wanqing Liu,Eden Haverfield,Mark J. Ratain	36
15	Comparison of performance of three commercial platforms for warfarin sensitivity genotyping 2009 ·Clinica Chimica Acta ·Nikolina Babić,Eden Haverfield,(unknown),(unknown),Soma Das,Kiang-Teck J. Yeo	10
16	SMC1Aexpression and mechanism of pathogenicity in probands with X-Linked Cornelia de Lange syndrome 2009 ·Human Mutation ·Jinglan Liu,(unknown),Zhe Zhang,Matthew A. Deardorff,Eden Haverfield,Maninder Kaur,(unknown),Dinah Clark,Antonie D. Kline,Darrel Waggoner,Soma Das,Laird G. Jackson,Ian D. Krantz	39
17	Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia 2008 ·European Journal of Human Genetics ·Eden Haverfield,(unknown),Kristin Petras,William B. Dobyns,Soma Das	51
18	Genetic evidence in support of a shared Eurasian-North African dairying origin 2005 ·Human Genetics ·Sean Myles,Nourdine Bouzekri,Eden Haverfield,Mohamed Cherkaoui,Jean‐Michel Dugoujon,Ryk Ward	56
19	Pharmacogenomics of Deferiprone Metabolism. 2005 ·Blood ·Eden Haverfield,D. J. Weatherall,(unknown),Jacqueline Ramı́rez,Mark J. Ratain	6
20	UGT1A1 variation and gallstone formation in sickle cell disease 2004 ·Blood ·Eden Haverfield,(unknown),Terrence Forrester,Nourdine Bouzekri,Rosalind M. Harding,G. R. Serjeant,Thomas Walker,Tim Peto,Ryk Ward,D. J. Weatherall	69

About Eden Haverfield

Eden Haverfield is a scholar working on Genetics, Clinical Biochemistry and Genetics, having authored 23 papers that have together received 536 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Genetics (277 citations), Genetics (67 citations) and Pediatrics, Perinatology and Child Health (95 citations). Eden Haverfield has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Ryk Ward, Nourdine Bouzekri, Soma Das, Kristin Petras, William B. Dobyns, Sean Myles, Jean‐Michel Dugoujon, Mohamed Cherkaoui, Wendy K. Chung and D. J. Weatherall. Their work appears in journals such as Blood, Cancer Research and Fertility and Sterility.

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