Corinne D. Boehm

5.2k total citations · 1 hit paper
38 papers, 3.3k citations indexed

About

Corinne D. Boehm is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Corinne D. Boehm has authored 38 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 18 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Corinne D. Boehm's work include Hemoglobinopathies and Related Disorders (17 papers), Prenatal Screening and Diagnostics (7 papers) and Parvovirus B19 Infection Studies (5 papers). Corinne D. Boehm is often cited by papers focused on Hemoglobinopathies and Related Disorders (17 papers), Prenatal Screening and Diagnostics (7 papers) and Parvovirus B19 Infection Studies (5 papers). Corinne D. Boehm collaborates with scholars based in United States, Singapore and Australia. Corinne D. Boehm's 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 and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

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 Stuart H. Orkin, Haig H. Kazazian et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Corinne D. Boehm United States	22	1.6k	1.4k	1.1k	812	470	38	3.3k
H H Kazazian United States	32	1.1k 0.7×	1.7k 1.2×	1.1k 1.0×	857 1.1×	273 0.6×	64	3.2k
Y Kan United States	23	1.1k 0.7×	1.5k 1.1×	742 0.7×	597 0.7×	245 0.5×	33	3.0k
Park S. Gerald United States	34	575 0.4×	1.8k 1.3×	473 0.4×	1.2k 1.4×	484 1.0×	111	3.6k
Helena Ayyub United Kingdom	27	832 0.5×	2.7k 1.9×	429 0.4×	1.0k 1.2×	270 0.6×	43	3.5k
G.J.B. van Ommen Netherlands	37	639 0.4×	3.3k 2.4×	140 0.1×	1.3k 1.6×	243 0.5×	91	4.8k
Richard J. Gibbons United Kingdom	42	1.1k 0.7×	5.3k 3.8×	621 0.6×	2.5k 3.1×	268 0.6×	104	6.9k
Stefan J. White Netherlands	31	410 0.3×	1.9k 1.4×	170 0.2×	1.3k 1.7×	301 0.6×	76	3.3k
Veronica J. Buckle United Kingdom	47	465 0.3×	4.6k 3.3×	516 0.5×	2.1k 2.6×	359 0.8×	91	6.5k
Shubha R. Phadke India	23	314 0.2×	908 0.7×	222 0.2×	826 1.0×	437 0.9×	268	2.4k
P. Nagesh Rao United States	26	345 0.2×	842 0.6×	523 0.5×	625 0.8×	272 0.6×	77	2.2k

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

Sobreira, Nara, Lisa G. Riley, Wendy Gold, et al.. (2017). Mutations in RARS cause a hypomyelination disorder akin to Pelizaeus–Merzbacher disease. European Journal of Human Genetics. 25(10). 1134–1141. 33 indexed citations

Alodaib, Ahmad, Nara Sobreira, Wendy Gold, et al.. (2016). Whole-exome sequencing identifies novel variants in PNPT1 causing oxidative phosphorylation defects and severe multisystem disease. European Journal of Human Genetics. 25(1). 79–84. 28 indexed citations

Hamosh, Ada, Nara Sobreira, Julie Hoover‐Fong, et al.. (2013). P heno DB : A New Web‐Based Tool for the Collection, Storage, and Analysis of Phenotypic Features. Human Mutation. 34(4). 566–571. 48 indexed citations

Stetten, Gail, et al.. (2008). Clinical consequences of an increasing trend of preferential use of cultured villi for molecular diagnosis by CVS. Prenatal Diagnosis. 28(4). 332–334. 4 indexed citations

Witmer, P. Dane, Kimberly F. Doheny, Corinne D. Boehm, et al.. (2003). The Development of a Highly Informative Mouse Simple Sequence Length Polymorphism (SSLP) Marker Set and Construction of a Mouse Family Tree Using Parsimony Analysis. Genome Research. 13(3). 485–491. 57 indexed citations

Kemp, Stephan, Aurora Pujol, Hans R. Waterham, et al.. (2001). ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations. Human Mutation. 18(6). 499–515. 214 indexed citations

Chong, Samuel S., Corinne D. Boehm, Garry R. Cutting, & Douglas R. Higgs. (2000). Simplified Multiplex-PCR Diagnosis of Common Southeast Asian Deletional Determinants of α-Thalassemia. Clinical Chemistry. 46(10). 1692–1695. 62 indexed citations

Boehm, Corinne D., et al.. (1999). Accurate DNA-Based Diagnostic and Carrier Testing for X-Linked Adrenoleukodystrophy. Molecular Genetics and Metabolism. 66(2). 128–136. 76 indexed citations

Kimberland, Michelle L., Corinne D. Boehm, & Haig H. Kazazian. (1995). Two novel β-thalassemia alleles: Poly A signal (AATAAA→AAAA) and −92 C→T. Human Mutation. 5(3). 275–276. 2 indexed citations

10.

Holmes, Susan E., et al.. (1994). A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion. Nature Genetics. 7(2). 143–148. 189 indexed citations

11.

Reiss, Allan L., Lisa S. Freund, Leslie Plotnick, et al.. (1993). The effects of X monosomy on brain development: Monozygotic twins discorcant for Turner's syndrome. Annals of Neurology. 34(1). 95–107. 88 indexed citations

12.

Hofman, Karen & Corinne D. Boehm. (1992). Familial neurofibromatosis type 1: Clinical experience with DNA testing. The Journal of Pediatrics. 120(3). 394–398. 17 indexed citations

13.

Kazazian, Haig H., et al.. (1990). Gene Defects in β‐Thalassemia and Their Prenatal Diagnosis. Annals of the New York Academy of Sciences. 612(1). 1–14. 20 indexed citations

14.

Boehm, Corinne D. & Haig H. Kazazian. (1990). The molecular basis of genetic disease. Current Opinion in Biotechnology. 1(2). 180–187. 4 indexed citations

15.

Long, Jeffrey C., Aravinda Chakravarti, Corinne D. Boehm, Stylianos E. Antonarakis, & Haig H. Kazazian. (1990). Phylogeny of human β‐globin haplotypes and its implications for recent human evolution. American Journal of Physical Anthropology. 81(1). 113–130. 61 indexed citations

16.

Maberry, Mark C., et al.. (1990). Alpha-Thalassemia: Prenatal Diagnosis and Neonatal Implications. American Journal of Perinatology. 7(4). 356–358. 5 indexed citations

17.

Kazazian, Haig H., Deborah G. Phillips, Carol E. Dowling, & Corinne D. Boehm. (1989). Prenatal Diagnosis of Sickle Cell Anemia—1988. Annals of the New York Academy of Sciences. 565(1). 44–47. 5 indexed citations

18.

LeRoy, Bonnie S., Corinne D. Boehm, Richard A. King, et al.. (1988). Identification of carriers of Duchenne muscular dystrophy: Value of molecular analysis. American Journal of Medical Genetics. 31(3). 709–721. 2 indexed citations

19.

Saiki, Randall K., et al.. (1988). Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes. New England Journal of Medicine. 319(9). 537–541. 230 indexed citations

20.

Orkin, Stuart H., Peter Little, Haig H. Kazazian, & Corinne D. Boehm. (1982). Improved Detection of the Sickle Mutation by DNA Analysis. New England Journal of Medicine. 307(1). 32–36. 138 indexed citations

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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