Eden Haverfield

2.8k citations

23 papers · 536 indexed · h-index 13

Genetics top 10%
- BRCA gene mutations in cancer 5
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 4
- Genetic Associations and Epidemiology 2
Genetics
- BRCA gene mutations in cancer 5
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 4
- Genetic Associations and Epidemiology 2
Pediatrics, Perinatology and Child Health top 10%
Hematology
Molecular Biology
- RNA modifications and cancer 3
- Biochemical and Molecular Research 2
- Protein Tyrosine Phosphatases 2
Clinical Biochemistry
- Metabolism and Genetic Disorders 2

Co-authors: Ryk Ward Nourdine Bouzekri Soma Das Kristin Petras William B. Dobyns Sean Myles Jean‐Michel Dugoujon Mohamed Cherkaoui
Cited by: Genetics Pediatrics, Perinatology and Child Health
Journals: Blood (2 papers)Cancer Research (1 paper)Fertility and Sterility (1 paper)
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

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

All Works

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20 of 20 papers shown

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

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