Beverly R. Akerman

1.1k citations

21 papers · 951 indexed · h-index 16

Co-authors: R A Gravel Barbara L. Triggs‐Raine Eileen P. Treacy Daniel Leclerc Cynthia G. Goodyer Andréa C. LeBlanc Omar Tounekti Alfonso León‐Del‐Río
Topics: Metabolism and Genetic Disorders (7 papers)Lysosomal Storage Disorders Research (7 papers)Child Nutrition and Feeding Issues (4 papers)
Cited by: Clinical Biochemistry Physiology Cell Biology
Journals: Proceedings of the National Academy of Sciences Journal of Neuroscience Human Molecular Genetics
Partner nations: Canada United States Australia

In The Last Decade

Beverly R. Akerman

21 papers receiving 937 citations

Peers

Countries citing papers authored by Beverly R. Akerman

Since Specialization

Citations

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

Fields of papers citing papers by Beverly R. Akerman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Beverly R. Akerman. 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 Beverly R. Akerman. The network helps show where Beverly R. Akerman may publish in the future.

Co-authorship network of co-authors of Beverly R. Akerman

This figure shows the co-authorship network connecting the top 25 collaborators of Beverly R. Akerman. A scholar is included among the top collaborators of Beverly R. Akerman 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 Beverly R. Akerman. Beverly R. Akerman 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	17-beta-estradiol induces an inhibitor of active caspases. 2001 ·PubMed ·Yan Zhang,Omar Tounekti,Beverly R. Akerman,Cynthia G. Goodyer,Andréa C. LeBlanc	68
2	17-β-Estradiol Induces an Inhibitor of Active Caspases 2001 ·Journal of Neuroscience ·Yan Zhang,Omar Tounekti,Beverly R. Akerman,Cynthia G. Goodyer,Andréa C. LeBlanc	56
3	Characterization of Phenylketonuria Missense Substitutions, Distant from the Phenylalanine Hydroxylase Active Site, Illustrates a Paradigm for Mechanism and Potential Modulation of Phenotype 2001 ·Molecular Genetics and Metabolism ·Paula J. Waters,Michael A. Parniak,Beverly R. Akerman,Charles R. Scriver	1
4	Characterization of Phenylketonuria Missense Substitutions, Distant from the Phenylalanine Hydroxylase Active Site, Illustrates a Paradigm for Mechanism and Potential Modulation of Phenotype 2000 ·Molecular Genetics and Metabolism ·Paula J. Waters,Michael A. Parniak,Beverly R. Akerman,Charles R. Scriver	44
5	Population-Specific Polymorphisms of the Human FMO3 Gene: Significance for Detoxication 2000 ·Drug Metabolism and Disposition ·John R. Cashman,Beverly R. Akerman,S. M. Forrest,Eileen P. Treacy	62
6	Caspases, amyloid metabolism and Alzheimer's disease 2000 ·Neurobiology of Aging ·Andréa C. LeBlanc,Beverly R. Akerman,Yan Zhang,(unknown),Catherine Bergeron	1
7	Trimethylaminuria Is Caused by Mutations of the FMO3 Gene in a North American Cohort 1999 ·Molecular Genetics and Metabolism ·Beverly R. Akerman,(unknown),Lionel M.L. Chow,Deborah M. Lambert,Cheryl R. Greenberg,(unknown),Orval Mamer,Eileen P. Treacy	60
8	Two novel mutations of theFMO3 gene in a proband with trimethylaminuria 1999 ·Human Mutation ·Beverly R. Akerman,S. M. Forrest,L. H. Chow,Rima Youil,Melanie A. Knight,Eileen P. Treacy	35
9	Missense mutations in the phenylalanine hydroxylase gene (PAH) can cause accelerated proteolytic turnover of PAH enzyme: A mechanism underlying phenylketonuria 1999 ·Journal of Inherited Metabolic Disease ·Paula J. Waters,Michael A. Parniak,Beverly R. Akerman,A Jones,C. R. Scriver	35
10	A frequent TG deletion near the polyadenylation signal of the human HEXB gene: Occurrence of an irregular DNA structure and conserved nucleotide sequence motif in the 3′ untranslated region 1998 ·Human Mutation ·(unknown),(unknown),Beverly R. Akerman,Raquel Dodelson de Kremer,R A Gravel,(unknown)	13
11	Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs disease. 1997 ·PubMed ·Beverly R. Akerman,Marvin R. Natowicz,Michael M. Kaback,Magali Loyer,Eric Campeau,R A Gravel	15
12	Dramatically Different Phenotypes in Mouse Models of Human Tay-Sachs and Sandhoff Diseases 1996 ·Human Molecular Genetics ·Daniel J. Phaneuf,Nobuaki Wakamatsu,Jingqi Huang,(unknown),Alan C. Peterson,Sheila R. Fortunato,Gerd Ritter,Suleiman A. Igdoura,Carlos R. Morales,(unknown),Beverly R. Akerman,Daniel Leclerc,Nobuo Hanai,Jamey D. Marth,Jacquetta M. Trasler,R A Gravel	204
13	A second, large deletion in the HEXB gene in a patient with infantile Sandhoff disease 1995 ·Human Molecular Genetics ·Zhixin Zhang,Nobuaki Wakamatsu,Beverly R. Akerman,(unknown),(unknown),Roy A. Gravel	14
14	Donor splice site mutation in intron 5 of theHEXA gene in a Turkish infant with Tay-Sachs disease 1995 ·Human Mutation ·(unknown),Beverly R. Akerman,G Ciliv,Meral Topçu,Yavuz Renda,(unknown)	17
15	Isolation of a cDNA encoding human holocarboxylase synthetase by functional complementation of a biotin auxotroph of Escherichia coli. 1995 ·Proceedings of the National Academy of Sciences ·Alfonso León‐Del‐Río,Daniel Leclerc,Beverly R. Akerman,(unknown),R A Gravel	81
16	Mutations participating in interallelic complementation in propionic acidemia. 1994 ·PubMed ·R A Gravel,Beverly R. Akerman,A.M. Lamhonwah,Magali Loyer,Alfonso León‐Del‐Río,(unknown)	38
17	Molecular basis of hexosamininidase a deficiency and pseudodeficiency in the Berks County Pennsylvania Dutch 1992 ·Human Mutation ·Emilie H. Mules,Susan J. Hayflick,Carol E. Dowling,Thaddeus E. Kelly,Beverly R. Akerman,Roy A. Gravel,(unknown)	20
18	A mutation common in non-jewish Tay-Sachs disease: Frequency and RNA studies 1992 ·Human Mutation ·Beverly R. Akerman,Julian Zielenski,Barbara L. Triggs‐Raine,E M Prence,Marvin R. Natowicz,(unknown),Michael M. Kaback,Emilie H. Mules,Gilles Thomas,Joe T.R. Clarke,R A Gravel	34
19	Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay-Sachs disease. 1991 ·PubMed ·Barbara L. Triggs‐Raine,Beverly R. Akerman,Joe T.R. Clarke,(unknown)	84
20	Identification of deletion and triple α‐globin gene haplotypes in the montreal β‐thalassemia screening program: Implications for genetic medicine 1990 ·American Journal of Medical Genetics ·Beverly R. Akerman,Takuya Fujiwara,Gerald Lancaster,Kenneth Morgan,Charles R. Scriver	5

About Beverly R. Akerman

Beverly R. Akerman is a scholar working on Clinical Biochemistry, Physiology and Psychiatry and Mental health, having authored 21 papers that have together received 951 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (7 papers), Lysosomal Storage Disorders Research (7 papers) and Child Nutrition and Feeding Issues (4 papers). The work is most often cited by research in Clinical Biochemistry (159 citations), Physiology (383 citations) and Cell Biology (225 citations). Beverly R. Akerman has collaborated with scholars based in Canada, United States and Australia. Frequent co-authors include R A Gravel, Barbara L. Triggs‐Raine, Eileen P. Treacy, Daniel Leclerc, Cynthia G. Goodyer, Andréa C. LeBlanc, Omar Tounekti, Alfonso León‐Del‐Río, S. M. Forrest and Joe T.R. Clarke. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and Human Molecular Genetics.

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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