Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

N. Bogdanova · SciRah

Researcher profile · Semantic Scholar

N. Bogdanova

Share profile

N. Bogdanova — researcher profile on SciRah

h-index: 20
Works: 59
Citations: 2,095

Most-cited papers

Comparison of phenotypes of polycystic kidney disease types 1 and 2. European PKD1-PKD2 Study Group.
N. Hateboer, M. A. Dijk, N. Bogdanova, E. Coto +5 more
1999The Lancet627 citations
Semantic Scholar
Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controls
F. Weiss, P. Simon, N. Bogdanova, J. Mayerle +3 more
2005Gut157 citations Open access
Semantic Scholar
Incompletely penetrant PKD1 alleles mimic the renal manifestations of ARPKD.
M. Vujić, C. M. Heyer, E. Ars, Katharina Hopp +8 more
2010Journal of the American Society of Nephrology153 citations Open access
Semantic Scholar
Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease.
R. Magistroni, N. He, Kai-Rong Wang, R. Andrew +20 more
2003Journal of the American Society of Nephrology130 citations Open access
Semantic Scholar
A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2).
B. Veldhuisen, J. Saris, S. de Haij, T. Hayashi +13 more
1997American Journal of Human Genetics101 citations Open access
Semantic Scholar
Gene expression patterns in relation to the clinical phenotype in Klinefelter syndrome.
M. Zitzmann, R. Bongers, S. Werler, N. Bogdanova +4 more
2015Journal of Clinical Endocrinology and Metabolism99 citations Open access
Semantic Scholar
Location of mutations within the PKD2 gene influences clinical outcome.
N. Hateboer, B. Veldhuisen, Dorien J. M. Peters, M. Breuning +13 more
2000Kidney International76 citations Open access
Semantic Scholar
Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A
N. Bogdanova, A. Markoff, R. Eisert, C. Wermes +5 more
2007Human Mutation66 citations Open access
Semantic Scholar
Genetic variation of DKK3 may modify renal disease severity in ADPKD.
Michelle Liu, S. Y. Shi, S. Senthilnathan, Julie L Yu +23 more
2010Journal of the American Society of Nephrology62 citations Open access
Semantic Scholar
CD34+ lineage specific donor cell chimerism for the diagnosis and treatment of impending relapse of AML or myelodysplastic syndrome after allo-SCT
F. Rosenow, A. Berkemeier, U. Krug, C. Müller-Tidow +10 more
2013Bone Marrow Transplantation52 citations
Semantic Scholar
Paternal and maternal carriage of the annexin A5 M2 haplotype are equal risk factors for recurrent pregnancy loss: a pilot study.
N. Rogenhofer, Laura Engels, N. Bogdanova, F. Tüttelmann +2 more
2012Fertility and Sterility50 citations Open access
Semantic Scholar
Evidence of a third ADPKD locus is not supported by reanalysis of designated PKD3 families
Binu M. Paul, Mark B. Consugar, MoonnohR . Lee, J. L. Sundsbak +11 more
2013Kidney International49 citations Open access
Semantic Scholar
Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A
N. Bogdanova, A. Markoff, H. Pollmann, U. Nowak-Göttl +6 more
2005Human Mutation48 citations
Semantic Scholar
Long-term secondary prophylaxis in children, adolescents and young adults with von Willebrand disease
S. Halimeh, A. Krümpel, H. Rott, N. Bogdanova +5 more
2011Thrombosis and Haemostasis46 citations
Semantic Scholar
Further insights into the role of the annexin A5 M2 haplotype as recurrent pregnancy loss factor, assessing timing of miscarriage and partner risk.
F. Tüttelmann, P. Ivanov, C. Dietzel, Ann-Kristin Sofroniou +5 more
2013Fertility and Sterility39 citations Open access
Semantic Scholar
Hereditary thrombophilic risk factors for recurrent pregnancy loss
A. Markoff, N. Bogdanova, M. Samama
2010Journal of Community Genetics35 citations Open access
Semantic Scholar
Effects of the FSH-β-subunit promoter polymorphism -211G->T on the hypothalamic-pituitary-ovarian axis in normally cycling women indicate a gender-specific regulation of gonadotropin secretion.
A. Schüring, A. Busch, N. Bogdanova, J. Gromoll +1 more
2013Journal of Clinical Endocrinology and Metabolism34 citations
Semantic Scholar
A large deletion and novel point mutations in the calpain 3 gene (CAPN3) in Bulgarian LGMD2A patients
A. Todorova, B. Georgieva, I. Tournev, T. Todorov +5 more
2007Neurogenetics27 citations
Semantic Scholar
Treacher Collins syndrome: clinical implications for the paediatrician—a new mutation in a severely affected newborn and comparison with three further patients with the same mutation, and review of the literature
J. Schlump, A. Stein, U. Hehr, T. Karen +8 more
2012European Journal of Pediatrics26 citations Open access
Semantic Scholar
Analysis of published PKD1 gene sequence variants
A. Gout, D. Ravine, Peter C. Harris, Sandro Rossetti +31 more
2007Nature Genetics21 citations
Semantic Scholar
Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A
N. Bogdanova, A. Markoff, H. Pollmann, U. Nowak-Göttl +4 more
2002Human Mutation20 citations Open access
Semantic Scholar
Independent association of the M2/ANXA5 haplotype with recurrent pregnancy loss (RPL) in PCOS patients.
N. Rogenhofer, Laura Engels, N. Bogdanova, F. Tüttelmann +2 more
2013Metabolism: Clinical and Experimental18 citations
Semantic Scholar
M2/ANXA5 haplotype as a predisposition factor in Malay women and couples experiencing recurrent spontaneous abortion: a pilot study.
Tang Thean Hock, N. Bogdanova, Ang Kai Cheen, Sushilnathan Kathirgamanathan +6 more
2015Reproductive Biomedicine Online16 citations Open access
Semantic Scholar
Genetic analysis of the M2/ANXA5 haplotype as recurrent pregnancy loss predisposition in the Malay population
Kai-Cheen Ang, Sushilnathan Kathirgamanathan, E. Ch'ng, Yania Lee +11 more
2017Journal of Assisted Reproduction and Genetics15 citations Open access
Semantic Scholar
Association between M2/ANXA5 haplotype and repeated pregnancy loss: a meta-analysis.
Kai-Cheen Ang, N. Bogdanova, A. Markoff, E. Ch'ng +1 more
2019Fertility and Sterility14 citations Open access
Semantic Scholar
Maternal and paternal carriage of the annexin A5 M2 haplotype: a possible risk factor for recurrent implantation failure (RIF)
N. Rogenhofer, A. Markoff, X. Ennerst, N. Bogdanova +1 more
2020Journal of Assisted Reproduction and Genetics13 citations Open access
Semantic Scholar
Maternal carriers of the ANXA5 M2 haplotype are exposed to a greater risk for placenta-mediated pregnancy complications
F. Aranda, S. Udry, Silvia Perés Wingeyer, L. C. Amshoff +5 more
2018Journal of Assisted Reproduction and Genetics11 citations Open access
Semantic Scholar
Functional characterisation of the CFTR mutations M348V and A1087P from patients with pancreatitis suggests functional interaction between CFTR monomers
F. Weiss, Peter Simon, N. Bogdanova, N. Shcheynikov +2 more
2009Gut10 citations
Semantic Scholar
Screening the 3′ region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutations
N. Bogdanova, M. McCluskey, Karin Sikmann, A. Markoff +7 more
2000Human Mutation10 citations Open access
Semantic Scholar
Autosomal Dominant Polycystic Kidney Disease – Clinical and Genetic Aspects
N. Bogdanova, A. Markoff, J. Horst
2002Kidney & Blood Pressure Research9 citations
Semantic Scholar
Seven novel and four recurrent point mutations in the factor VIII (F8C) gene
N. Bogdanova, B. Lemcke, A. Markoff, H. Pollmann +3 more
2001Human Mutation9 citations Open access
Semantic Scholar
Inhibitor-Immunology-Study
I. Wieland, C. Wermes, B. Eifrig, K. Holstein +12 more
2011Hämostaseologie7 citations
Semantic Scholar
Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1‐linked Australian families
M. McCluskey, T. Schiavello, Michael Hunter, Janina Hantke +7 more
2002Human Mutation7 citations Open access
Semantic Scholar
The haplotype M2 of the ANXA5 gene is not associated with antitrophoblast antibodies
N. Rogenhofer, Laura Engels, N. Bogdanova, F. Tüttelmann +2 more
2013Journal of Assisted Reproduction and Genetics6 citations Open access
Semantic Scholar
Genetic Predispositions to Thrombophilia Associated with Recurrent Pregnancy Loss
N. Bogdanova, A. Markoff
20085 citations
Semantic Scholar
Influence of factor 5 rs6025 and factor 2 rs1799963 mutation on inhibitor development in patients with hemophilia A--an Israeli-German multicenter database study.
G. Kenet, C. Bidlingmaier, N. Bogdanova, C. Ettingshausen +8 more
2014Thrombosis Research4 citations Open access
Semantic Scholar
Intervention of Low-Molecular-Weight Heparin in M2/ANXA5 Haplotype Carriers: A Case Report in Pregnancy
Kai-Cheen Ang, A. Roslani, N. Bogdanova, P. Wieacker +2 more
20173 citations
Semantic Scholar
Annexin A5 haplotype M2 is not a risk factor for recurrent spontaneous abortion in Northern Europe: is there sufficient evidence?
A. Markoff, H. Kurahashi, E. Grandone, N. Bogdanova
2016Reproductive Biomedicine Online3 citations Open access
Semantic Scholar
Lower Incidence of M2/ANXA5 Carriage in Recurrent Pregnancy Loss Patients With Elevated Lipoprotein(a) Levels
N. Rogenhofer, Laura Engels, N. Bogdanova, F. Tüttelmann +2 more
2014Clinical and applied thrombosis/hemostasis3 citations Open access
Semantic Scholar
Ten novel factor VIII (F8C) mutations in eighteen haemophilia A families detected in Singapore
A. Abdul-Ghafar, N. Bogdanova, L. Lim, Y. Zhao +2 more
2009Haemophilia3 citations
Semantic Scholar
THE ROLE OF HYPOXIA IN THE DEVELOPMENT OF SOME PATHOLOGICAL CONDITIONS AND MALIGNANT TUMORS
N. Bogdanova, N. H. Pogorela, E. Lukyanetz
20212 citations Open access
Semantic Scholar
The relevance of ANXA5 genetic variants on male fertility
H. Lavorato, A. Markoff, Valeria Altholz, N. Bogdanova +3 more
2019Journal of Assisted Reproduction and Genetics2 citations Open access
Semantic Scholar
Elevated annexin A5 plasma levels in term pregnancies of M2/ANXA5 carriers.
Kai-Cheen Ang, Sushilnathan Kathirgamanathan, E. Ch'ng, W. Abdullah +7 more
2017Thrombosis Research2 citations
Semantic Scholar
Intrafamilial phenotypic variability of Specific Language Impairment.
L. Bartha-Doering, Sabrina Regele, D. Deuster, R. Seidl +4 more
2016Brain and Language2 citations
Semantic Scholar
Novel MLH1 frameshift mutation in an extended hereditary nonpolyposis colorectal cancer family.
T. Kadiyska, R. Kaneva, D. Nedin, A. Alexandrova +7 more
2006World Journal of Gastroenterology2 citations Open access
Semantic Scholar
The M2 haplotype of ANXA5 gene in the context of unexplained recurrent miscarriages
A. Markoff, N. Bogdanova
2017Journal of Community Genetics1 citations Open access
Semantic Scholar
Development of cost-effective and accurate allele-specific PCR for determination of M2/ANXA5 haplotype in recurrent pregnancy loss
Kai-Cheen Ang, Timofey S. Rozhdestvensky, A. Markoff, N. Bogdanova +2 more
20210 citations Open access
Semantic Scholar
The M2 haplotype of ANXA5 gene in the context of unexplained recurrent miscarriages
A. Markoff, N. Bogdanova
2017Journal of Community Genetics0 citations Open access
Semantic Scholar
Authors' response to the letter of Nagirnaja et al., "Response to annexin A5 haplotype M2 is not a risk factor for recurrent miscarriages in Northern Europe, is there sufficient evidence?".
A. Markoff, H. Kurahashi, E. Grandone, N. Bogdanova
2016Reproductive Biomedicine Online0 citations Open access
Semantic Scholar
Haplotypes and polymorphisms of the ANXA5 nontranslated region in Japanese and European women with recurrent miscarriage and in controls.
A. Markoff, N. Bogdanova
2014Fertility and Sterility0 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

A. Markoff×30
Invite
A. Markoff — researcher profile on SciRah
P. Wieacker×9
Invite
P. Wieacker — researcher profile on SciRah
F. Tüttelmann×7
Invite
F. Tüttelmann — researcher profile on SciRah
J. Horst×7
Invite
J. Horst — researcher profile on SciRah

×6

Invite

B. Dworniczak — researcher profile on SciRah

Invite

R. Torra — researcher profile on SciRah

Invite

H. Pollmann — researcher profile on SciRah

U. Nowak-Göttl×5

Invite

U. Nowak-Göttl — researcher profile on SciRah

N. Rogenhofer×5

Invite

N. Rogenhofer — researcher profile on SciRah

Invite

C. Thaler — researcher profile on SciRah

Kai-Cheen Ang×5

Invite

Kai-Cheen Ang — researcher profile on SciRah

Thean-Hock Tang×5

Invite

Thean-Hock Tang — researcher profile on SciRah