Evidence map›Paper›PMID 42434306›Full record

ArticleFrontiers in endocrinology2026

Functional and clinical evidence for two novel heterozygous

Tian-Ying Wei, Ming-Xian Kang, Ge-Han Zhang, Jing Zhang, Jia-En Liu, Jing Ma, Ya-Ping Tian, Hua-Ying Hu

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Tian-Ying WeiBeijing Jiaen Hospital, Heen Life Medical Research Institute, Beijing, China.
Ming-Xian KangBeijing Jiaen Hospital, Heen Life Medical Research Institute, Beijing, China.
Ge-Han ZhangMedical Innovation Research Division of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Jing ZhangPrenatal Diagnosis Center, Shijiazhuang Obstetrics and Gynecology Hospital, Hebei Key Laboratory of Maternal and Fetal Medicine, Shijiazhuang, Hebei, China.
Jia-En LiuBeijing Jiaen Hospital, Heen Life Medical Research Institute, Beijing, China.
Jing MaHebei Key Laboratory of Reproductive Medicine, Hebei Reproductive Health Hospital, Shijiazhuang, Hebei, China.
Ya-Ping TianMedical Innovation Research Division of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Hua-Ying HuMedical Innovation Research Division of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Recurrent pregnancy loss (RPL) is a common reproductive disorder with largely unexplained etiology. Premature chromatid separation (PCS), a cytogenetic manifestation of chromosomal instability, is linked to spindle assembly checkpoint (SAC) dysfunction. While biallelic Methods: Here, we investigated two unrelated families with unexplained RPL. Chromosomal microarray analysis of six miscarriage specimens revealed random aneuploidies. Whole-exome sequencing identified two novel heterozygous Results: Two novel heterozygous Discussion: These findings provide the first clinical evidence suggesting that heterozygous

Indexed as

Abortion, HabitualCell Cycle ProteinsGenetic CounselingProtein Serine-Threonine KinasesAdultExome SequencingFemaleHeterozygoteHumansMaleMutation, MissensePedigreePregnancyBUB1B protein, humanCell Cycle ProteinsProtein Serine-Threonine KinasesaneuploidyBUB1Bgenetic diagnosispremature chromatid separationrecurrent pregnancy loss

Identifiers

PMID42434306
PMCPMC13349884

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.