Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetics of suspected thrombophilia in Serbian females with infertility, including three cases, homozygous for FII 20210A or FV 1691A mutations.

Human fertility (Cambridge, England) - 1 Jun 2017

Djurovic Jelena, Stojkovic Oliver, Todorovic Jelena, Brajic Aleksandra, Stankovic Sanja, Obradovic Svetlana, Stamenkovic Gorana

Abstract excerpt

Reproductive failure (recurrent foetal loss, unexplained infertility and IVF implantation failure) may be, in a number of cases, explained by thrombophilia, either acquired or inherited. Several genes contribute to thrombophilia, some with major effect (Factor V, Factor II), and some with minor effect (MTHFR, PAI-1, ATIII, etc.). The aim of this study was to estimate frequency of thrombophilia-associated...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Abortion, Habitual
Share to Blood Coagulation Factors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Expression Regulation

Share to Genetic Predisposition to Disease

Share to Genotype

Share to Infertility, Female

Share to Serbia

Share to Thrombophilia

Source

Identifiers

PMID: 27855570
DOI: 10.1080/14647273.2016.1255785

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetics of suspected thrombophilia in Serbian females with infertility, including three cases, homozygous for FII 20210A or FV 1691A mutations.PMID 27855570Read ↗

Prevalence of F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms in Bosnian women with pregnancy loss.Semantic proximity Read ↗

Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion.Semantic proximity Read ↗

[Inherited thrombophilic factors in women with secondary infertility].Semantic proximity Read ↗

Association between FVL G1691A, FII G20210A, and MTHFR C677T and A1298C polymorphisms and Turkish women with recurrent pregnancy loss.Semantic proximity Read ↗

Which are the most common thrombophilic genetic nucleotide polymorphisms in infertile women undergoing an IVF cycle?Semantic proximity Read ↗

Genetic markers for inherited thrombophilia related pregnancy loss and implantation failure in Indian population - implications for diagnosis and clinical management.Semantic proximity Read ↗

[The role of 1691G>A (Leiden) mutation in Factor V gene, 20210G>A in prothrombin gene and 677C>T in MTHFR gene in etiology of early pregnancy loss].Semantic proximity Read ↗

Inherited thrombophilia in republic of Georgia women with or without a personal and/or family history of thrombosis and unexplained recurrent pregnancy loss.Semantic proximity Read ↗

The association between thrombophilic genes alterations and poor ovarian response in infertile women: a retrospective case-control study.Semantic proximity Read ↗

Prevalence of genetic prothrombotic risk factors: 1691G > A FV, 20210G > A PT and 677C > T MTHFR mutations in the Bosnian population.Semantic proximity Read ↗

[Factor V Leiden, FII G20210A, MTHFR C677T mutations as risk factors for venous thrombosis during pregnancy and puerperium].Semantic proximity Read ↗

The impact of heterozygosity for the factor V Leiden and factor II G20210A mutations on the risk of thrombosis in Greek patients.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.