Corinne D. Boehm

5.2k citations

38 papers · 3.3k indexed · 1 hit paper · h-index 22

Genetics top 0.5%
Molecular Biology top 5%
Hematology top 0.5%
Genetics top 2%
Pediatrics, Perinatology and Child Health top 2%

Co-authors: Haig H. Kazazian Stylianos E. Antonarakis Patricia J. Giardina Garry R. Cutting Stuart H. Orkin Samuel S. Chong Douglas R. Higgs Sabra C. Goff
Topics: Hemoglobinopathies and Related Disorders (17 papers)Prenatal Screening and Diagnostics (7 papers)Parvovirus B19 Infection Studies (5 papers)
Cited by: Genetics Hematology
Journals: Nature New England Journal of Medicine Proceedings of the National Academy of Sciences
Partner nations: United States Singapore Australia

In The Last Decade

Corinne D. Boehm

38 papers receiving 3.1k 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.

Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster

1982 822 citations Haig H. Kazazian, Stylianos E. Antonarakis et al. profile →

Peers

Countries citing papers authored by Corinne D. Boehm

Since Specialization

Citations

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

Fields of papers citing papers by Corinne D. Boehm

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Corinne D. Boehm. 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 Corinne D. Boehm. The network helps show where Corinne D. Boehm may publish in the future.

Co-authorship network of co-authors of Corinne D. Boehm

This figure shows the co-authorship network connecting the top 25 collaborators of Corinne D. Boehm. A scholar is included among the top collaborators of Corinne D. Boehm 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 Corinne D. Boehm. Corinne D. Boehm 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	Mutations in RARS cause a hypomyelination disorder akin to Pelizaeus–Merzbacher disease 2017 ·European Journal of Human Genetics ·(unknown),Nara Sobreira,Lisa G. Riley,Wendy Gold,Birgit Uhlenberg,Claudia Weiß,Corinne D. Boehm,Kristina Prelog,Robert Ouvrier,John Christodoulou	33
2	Whole-exome sequencing identifies novel variants in PNPT1 causing oxidative phosphorylation defects and severe multisystem disease 2016 ·European Journal of Human Genetics ·Ahmad Alodaib,Nara Sobreira,Wendy Gold,Lisa G. Riley,Nicole J. Van Bergen,Meredith Wilson,Bruce Bennetts,David R. Thorburn,Corinne D. Boehm,John Christodoulou	28
3	P heno DB : A New Web‐Based Tool for the Collection, Storage, and Analysis of Phenotypic Features 2013 ·Human Mutation ·Ada Hamosh,Nara Sobreira,Julie Hoover‐Fong,V. Reid Sutton,Corinne D. Boehm,François Schiettecatte,David Valle	48
4	Clinical consequences of an increasing trend of preferential use of cultured villi for molecular diagnosis by CVS 2008 ·Prenatal Diagnosis ·(unknown),(unknown),(unknown),Gail Stetten,(unknown),Corinne D. Boehm,Karin J. Blakemore	4
5	The Development of a Highly Informative Mouse Simple Sequence Length Polymorphism (SSLP) Marker Set and Construction of a Mouse Family Tree Using Parsimony Analysis 2003 ·Genome Research ·P. Dane Witmer,Kimberly F. Doheny,(unknown),Corinne D. Boehm,(unknown),Janet L. Goldstein,(unknown),(unknown),(unknown),Elizabeth Pugh,Robert L. Nussbaum,Kent W. Hunter,(unknown),Lucy B. Rowe,Michael Brownstein	57
6	ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations 2001 ·Human Mutation ·Stephan Kemp,Aurora Pujol,Hans R. Waterham,(unknown),Corinne D. Boehm,Gerald V. Raymond,Garry R. Cutting,Ronald J. A. Wanders,Hugo W. Moser	214
7	Simplified Multiplex-PCR Diagnosis of Common Southeast Asian Deletional Determinants of α-Thalassemia 2000 ·Clinical Chemistry ·Samuel S. Chong,Corinne D. Boehm,Garry R. Cutting,Douglas R. Higgs	62
8	Accurate DNA-Based Diagnostic and Carrier Testing for X-Linked Adrenoleukodystrophy 1999 ·Molecular Genetics and Metabolism ·Corinne D. Boehm,Garry R. Cutting,(unknown),Hugo W. Moser,Samuel S. Chong	76
9	Practical guide to the diagnosis of thalassemia 1996 ·American Journal of Medical Genetics ·Kenneth W. Dumars,Corinne D. Boehm,James R. Eckman,Patricia J. Giardina,Peter A. Lane,Frank Shafer	25
10	Two novel β-thalassemia alleles: Poly A signal (AATAAA→AAAA) and −92 C→T 1995 ·Human Mutation ·Michelle L. Kimberland,Corinne D. Boehm,Haig H. Kazazian	2
11	A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion 1994 ·Nature Genetics ·Susan E. Holmes,Beth A. Dombroski,(unknown),Corinne D. Boehm,Haig H. Kazazian	189
12	The effects of X monosomy on brain development: Monozygotic twins discorcant for Turner's syndrome 1993 ·Annals of Neurology ·Allan L. Reiss,Lisa S. Freund,Leslie Plotnick,Thomas L. Baumgardner,Kathleen Green,(unknown),Mark Reader,Corinne D. Boehm,Martha B. Denckla	88
13	Familial neurofibromatosis type 1: Clinical experience with DNA testing 1992 ·The Journal of Pediatrics ·Karen Hofman,Corinne D. Boehm	17
14	The molecular basis of genetic disease 1990 ·Current Opinion in Biotechnology ·Corinne D. Boehm,Haig H. Kazazian	4
15	Alpha-Thalassemia: Prenatal Diagnosis and Neonatal Implications 1990 ·American Journal of Perinatology ·Mark C. Maberry,Victor Klein,Corinne D. Boehm,(unknown),Larry C. Gilstrap	5
16	Phylogeny of human β‐globin haplotypes and its implications for recent human evolution 1990 ·American Journal of Physical Anthropology ·Jeffrey C. Long,Aravinda Chakravarti,Corinne D. Boehm,Stylianos E. Antonarakis,Haig H. Kazazian	61
17	Gene Defects in β‐Thalassemia and Their Prenatal Diagnosis 1990 ·Annals of the New York Academy of Sciences ·Haig H. Kazazian,Carol E. Dowling,Corinne D. Boehm,(unknown),(unknown),Joel Katz,Stylianos E. Antonarakis	20
18	Prenatal Diagnosis of Sickle Cell Anemia—1988 1989 ·Annals of the New York Academy of Sciences ·Haig H. Kazazian,Deborah G. Phillips,Carol E. Dowling,Corinne D. Boehm	5
19	Identification of carriers of Duchenne muscular dystrophy: Value of molecular analysis 1988 ·American Journal of Medical Genetics ·Bonnie S. LeRoy,(unknown),(unknown),Corinne D. Boehm,Richard A. King,Stephen S. Rich,Preston Williams,Stephen A. Smith,Bérengère de Martinville,James F. Reynolds	2
20	Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes 1988 ·New England Journal of Medicine ·Randall K. Saiki,C. C. Chang,Corey Levenson,(unknown),Corinne D. Boehm,Haig H. Kazazian,(unknown)	230

About Corinne D. Boehm

Corinne D. Boehm is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health, having authored 38 papers that have together received 3.3k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (17 papers), Prenatal Screening and Diagnostics (7 papers) and Parvovirus B19 Infection Studies (5 papers). The work is most often cited by research in Genetics (1.6k citations), Hematology (1.1k citations) and Genetics (812 citations). Corinne D. Boehm has collaborated with scholars based in United States, Singapore and Australia. Frequent co-authors include Haig H. Kazazian, Stylianos E. Antonarakis, Patricia J. Giardina, Garry R. Cutting, Stuart H. Orkin, Samuel S. Chong, Douglas R. Higgs, Sabra C. Goff, Julianne P. Sexton and Pamela Waber. Their work appears in journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

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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