Laura M. Tanner

Helsinki, Finland

Last Updated: 09/26/2026

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Found 26 publications

Perinatal outcomes in 35 children with cartilage hair hypoplasia.

Perinatal outcomes in 35 children with cartilage hair hypoplasia.

Journal: Orphanet journal of rare diseases

Published: June 23, 2025

The Role of Prenatal Ultrasound and Added Value of Post-Mortem Radiographic Imaging With X-Ray and CT in Suspected Fetal Skeletal Dysplasia.

The Role of Prenatal Ultrasound and Added Value of Post-Mortem Radiographic Imaging With X-Ray and CT in Suspected Fetal Skeletal Dysplasia.

Journal: Prenatal diagnosis

Published: September 26, 2024

Infertility following trisomic pregnancies: A nationwide cohort study.

Infertility following trisomic pregnancies: A nationwide cohort study.

Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics

Published: June 06, 2024

Lysinuric Protein Intolerance and Its Nutritional and Multisystemic Challenges in Pregnancy: A Case Report and Literature Review.

Lysinuric Protein Intolerance and Its Nutritional and Multisystemic Challenges in Pregnancy: A Case Report and Literature Review.

Journal: Journal of clinical medicine

Published: September 14, 2023

Plasma calprotectin is extremely high in patients with lysinuric protein intolerance.

Plasma calprotectin is extremely high in patients with lysinuric protein intolerance.

Journal: JIMD reports

Published: March 09, 2023

X-linked pyruvate dehydrogenase complex deficiency due to a novel PDHA1 variant associated with structural brain abnormalities in a fetus.

X-linked pyruvate dehydrogenase complex deficiency due to a novel PDHA1 variant associated with structural brain abnormalities in a fetus.

Journal: Prenatal diagnosis

Published: January 26, 2023

Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohort.

Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohort.

Journal: Prenatal diagnosis

Published: March 04, 2022

Platelet function and filamin A expression in two families with novel FLNA gene mutations associated with periventricular nodular heterotopia and panlobular emphysema.

Platelet function and filamin A expression in two families with novel FLNA gene mutations associated with periventricular nodular heterotopia and panlobular emphysema.

Journal: American journal of medical genetics. Part A

Published: May 03, 2021

Prenatal array comparative genomic hybridization in a well-defined cohort of high-risk pregnancies. A 3-year implementation results in a public tertiary academic referral hospital.

Prenatal array comparative genomic hybridization in a well-defined cohort of high-risk pregnancies. A 3-year implementation results in a public tertiary academic referral hospital.

Journal: Prenatal diagnosis

Published: April 24, 2020

APOE Genotype Disclosure and Lifestyle Advice in a Randomized Intervention Study with Finnish Participants.

APOE Genotype Disclosure and Lifestyle Advice in a Randomized Intervention Study with Finnish Participants.

Journal: The Journal of nutrition

Published: December 31, 2019

A Long-Term Follow-Up Study on Disclosing Genetic Risk Information (APOE) to Promote Healthy Lifestyles in Finland.

A Long-Term Follow-Up Study on Disclosing Genetic Risk Information (APOE) to Promote Healthy Lifestyles in Finland.

Journal: Lifestyle genomics

Published: December 05, 2018

Abnormal coagulation and enhanced fibrinolysis due to lysinuric protein intolerance associates with bleeds and renal impairment.

Abnormal coagulation and enhanced fibrinolysis due to lysinuric protein intolerance associates with bleeds and renal impairment.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: May 12, 2018

Showing 1-12 of 26

Last Updated: 09/26/2026