Dimitar N. Azmanov

1.8k citations

23 papers · 336 indexed · h-index 12

Co-authors: Luba Kalaydjieva Ivailo Tournev Velina Guergueltcheva Teodora Chamova Bharti Morar Michael Bynevelt Ara Kaprelyan Laura V. Flórez
Topics: Genomics and Rare Diseases (7 papers)Genetic Syndromes and Imprinting (7 papers)Genomic variations and chromosomal abnormalities (5 papers)
Cited by: Genetics Cellular and Molecular Neuroscience Clinical Biochemistry
Journals: The American Journal of Human Genetics Human Molecular Genetics Gene
Partner nations: Australia Bulgaria United Kingdom

In The Last Decade

Dimitar N. Azmanov

21 papers receiving 329 citations

Peers

Countries citing papers authored by Dimitar N. Azmanov

Since Specialization

Citations

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

Fields of papers citing papers by Dimitar N. Azmanov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dimitar N. Azmanov. 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 Dimitar N. Azmanov. The network helps show where Dimitar N. Azmanov may publish in the future.

Co-authorship network of co-authors of Dimitar N. Azmanov

This figure shows the co-authorship network connecting the top 25 collaborators of Dimitar N. Azmanov. A scholar is included among the top collaborators of Dimitar N. Azmanov 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 Dimitar N. Azmanov. Dimitar N. Azmanov 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	Epilepsy surgery in PCDH 19 related developmental and epileptic encephalopathy: A case report 2022 ·Epilepsy & Behavior Reports ·Lakshmi Nagarajan,Soumya Ghosh,(unknown),Sharon Lee,Jonathan Silberstein,Dimitar N. Azmanov,(unknown)	4
2	Studying Disease-Associated UBE3A Missense Variants Using Enhanced Sampling Molecular Simulations 2022 ·ACS Omega ·Mark Agostino,F. Ellis McKenzie,(unknown),Karen Woodward,(unknown),Dimitar N. Azmanov,Julian Ik‐Tsen Heng	0
3	Further heterogeneity in Silver–Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement 2021 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Karen Woodward,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Gillian M. Arscott,John Beilby,Catherine S. Choong,Sharron Townshend,Dimitar N. Azmanov	5
4	Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay 2021 ·Molecular Case Studies ·Ram J. Singh,Ana S.A. Cohen,(unknown),(unknown),(unknown),Geetu Mendiratta,Wahab Khan,Dimitar N. Azmanov,Karen Woodward,Maria Kirchhoff,Lisong Shi,Lisa Edelmann,Gareth Baynam,Stuart A. Scott,Ethylin Wang Jabs	3
5	A homozygous UBA5 pathogenic variant causes a fatal congenital neuropathy 2020 ·Journal of Medical Genetics ·Macarena Cabrera‐Serrano,David Coote,Dimitar N. Azmanov,Hayley Goullée,Erik Andersen,Catriona McLean,Mark R. Davis,Ryosuke Ishimura,Zornitza Stark,Jean‐Michel Vallat,Masaaki Komatsu,Andrew J. Kornberg,Monique M. Ryan,Nigel G. Laing,Gianina Ravenscroft	19
6	Tricho-hepatic-enteric syndrome (THES) without intractable diarrhoea 2019 ·Gene ·(unknown),Gopal P. Pathak,(unknown),(unknown),Dimitar N. Azmanov,(unknown),(unknown),(unknown),(unknown),Erin B. Taylor,Michael O’Sullivan,(unknown),Madhur Ravikumara,H. Dawkins,Nicholas Pachter,Gareth Baynam	12
7	Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy 2018 ·npj Genomic Medicine ·Mark Corbett,Clare L. van Eyk,Dani L. Webber,Stephen J. Bent,Morgan Newman,Kelly Harper,Jesia G. Berry,Dimitar N. Azmanov,Karen Woodward,Alison Gardner,Jennie Slee,Luis A. Pérez‐Jurado,Alastair H. MacLennan,Jozef Gécz	27
8	Transcriptome-wide effects of aPOLR3Agene mutation in patients with an unusual phenotype of striatal involvement 2016 ·Human Molecular Genetics ·Dimitar N. Azmanov,Stefan J. Siira,Teodora Chamova,Ara Kaprelyan,Velina Guergueltcheva,Anne-Marie J. Shearwood,Ganqiang Liu,Bharti Morar,Oliver Rackham,Michael Bynevelt,(unknown),Zdravko Kamenov,(unknown),Ivailo Tournev,Luba Kalaydjieva,Aleksandra Filipovska	38
9	Mosaic dominant TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia 2015 ·Movement Disorders ·Daliya Kancheva,Teodora Chamova,Velina Guergueltcheva,Vanio Mitev,Dimitar N. Azmanov,Luba Kalaydjieva,Ivailo Tournev,Albena Jordanova	27
10	Mosaic Genome-Wide uniparental disomy (GW-UPD): Heterogeneity of a rare disorder poses diagnostic and management challenges 2014 ·Pathology ·Dimitar N. Azmanov,Matthew Edwards,(unknown),Karen Carpenter,Karen Woodward,Kym Mina	2
11	Autosomal-Recessive Congenital Cerebellar Ataxia Is Caused by Mutations in Metabotropic Glutamate Receptor 1 2012 ·The American Journal of Human Genetics ·Velina Guergueltcheva,Dimitar N. Azmanov,Dora Angelicheva,Katherine R. Smith,Teodora Chamova,Laura V. Flórez,Michael Bynevelt,Thai B. Nguyen,Sylvia Cherninkova,Veneta Bojinova,Ara Kaprelyan,(unknown),Bharti Morar,David Chandler,Radka Kaneva,Melanie Bahlo,Ivailo Tournev,Luba Kalaydjieva	69
12	Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic dysplasia 2011 ·European Journal of Human Genetics ·(unknown),Miriam Aza‐Carmona,Eva Barroso,Damián Heine‐Suñer,Dimitar N. Azmanov,Jordi Rosell,Begoña Ezquieta,(unknown),(unknown),Jaime Cruz‐Rojo,Fernando Santos,José Ignacio Rodrı́guez,(unknown),Jesús Argente,Luba Kalaydjieva,Ricardo Gracía,Ángel Campos‐Barros,Sara Benito‐Sanz,Karen E. Heath	8
13	Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3 2011 ·Epilepsy Research ·Dimitar N. Azmanov,(unknown),(unknown),Bharti Morar,Dora Angelicheva,Dora Zlatareva,Radka Kaneva,Ivailo Tournev,Luba Kalaydjieva,Josemir W. Sander	7
14	A novel GEFS+ locus on 12p13.33 in a large Roma family 2011 ·Epilepsy Research ·Bharti Morar,(unknown),Dimitar N. Azmanov,(unknown),Dora Angelicheva,Velina Guergueltcheva,Radka Kaneva,Ingrid E. Scheffer,Ivailo Tournev,Luba Kalaydjieva,Josemir W. Sander	5
15	Mosaicism of a missenseSCN1Amutation and Dravet syndrome in a Roma/Gypsy family 2010 ·Epileptic Disorders ·Dimitar N. Azmanov,(unknown),(unknown),(unknown),Veneta Bojinova,Laura V. Flórez,Shelagh Smith,Ivailo Tournev,Assen Jablensky,John C. Mulley,Ingrid E. Scheffer,Luba Kalaydjieva,Josemir W. Sander	14
16	Partial epilepsy syndrome in a Gypsy family linked to 5q31.3‐q32 2009 ·Epilepsia ·Dora Angelicheva,Ivailo Tournev,Velina Guergueltcheva,Violeta Mihaylova,Dimitar N. Azmanov,Bharti Morar,(unknown),Shelagh Smith,Dora Zlatareva,John Stevens,Radka Kaneva,Veneta Bojinova,Kim W. Carter,Matthew A. Brown,Assen Jablensky,Luba Kalaydjieva,Josemir W. Sander	15
17	Further evidence for allelic heterogeneity in Hartnup disorder 2008 ·Human Mutation ·Dimitar N. Azmanov,(unknown),Helen Rodgers,Christiane Auray‐Blais,Robert Giguère,John E.J. Rasko,Stefan Bröer,Juleen A. Cavanaugh	15
18	Persistence of the Common Hartnup Disease D173N Allele in Populations of European Origin 2007 ·Annals of Human Genetics ·Dimitar N. Azmanov,Helen Rodgers,Christiane Auray‐Blais,Robert Giguère,Charles G. Bailey,Stefan Bröer,John E.J. Rasko,Juleen A. Cavanaugh	13
19	Profile of chromosomal aberrations in different gestational age spontaneous abortions detected by comparative genomic hybridization 2006 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·Dimitar N. Azmanov,(unknown),Boriana Zaharieva,(unknown),(unknown),(unknown),(unknown),(unknown),Драга Тончева	27
20	Apoptosis can be induced by Lontrel 2004 ·Comptes Rendus De L Academie Bulgare Des Sciences ·(unknown),Dimitar N. Azmanov,Gabriele Jovtchev,(unknown),(unknown),(unknown)	1

About Dimitar N. Azmanov

Dimitar N. Azmanov is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 23 papers that have together received 336 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Genetic Syndromes and Imprinting (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). The work is most often cited by research in Genetics (122 citations), Cellular and Molecular Neuroscience (75 citations) and Clinical Biochemistry (26 citations). Dimitar N. Azmanov has collaborated with scholars based in Australia, Bulgaria and United Kingdom. Frequent co-authors include Luba Kalaydjieva, Ivailo Tournev, Velina Guergueltcheva, Teodora Chamova, Bharti Morar, Michael Bynevelt, Ara Kaprelyan, Laura V. Flórez, Dora Angelicheva and Radka Kaneva. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics and Gene.

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