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Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome

American journal of medical genetics. Part A, 2020-05, Vol.182 (5), p.1273-1277

2020

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Debate 5: All Women with Recurrent Implantation Failure Should Be Offered PGT-A: Motion For – Author: Tristan Hardy; Motion Against – Author: Richard Legro

Fertility & reproduction, 2023-12, Vol.5 (4), p.314-314

2023

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Diagnosis of adolescent polycystic ovary syndrome

Steroids, 2013-08, Vol.78 (8), p.751-754

2013

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Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal services

Australian & New Zealand journal of obstetrics & gynaecology, 2024-04

2024

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The role of prenatal diagnosis following preimplantation genetic testing for single‐gene conditions: A historical overview of evolving technologies and clinical practice

Prenatal diagnosis, 2020-05, Vol.40 (6), p.647-651

Hardy, Tristan

2020

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Reproductive carrier screening

Pathology, 2024-02, Vol.56, p.S20

Hardy, Tristan

2024

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Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas

Journal of the Endocrine Society, 2020-12, Vol.4 (12), p.bvaa071-bvaa071

2020

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Variation in the Incidence and Type of Full versus Mosaic Segmental Aneuploidies Identified in Blastocysts Undergoing PGT-A

Fertility & reproduction, 2024-03, Vol.6 (1), p.15-22

2024

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Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes

Frontiers in genetics, 2022-08, Vol.13, p.975987-975987

2022

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Illuminating the Artefacts of NGS Seen in PGT-A & PGT-SR

Fertility & reproduction, 2022-09, Vol.4 (3n04), p.216-216

2022

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Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium

Molecular cytogenetics, 2024-04, Vol.17 (1), p.9-9, Article 9

2024

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Does Advanced Paternal Age Increase the Rate of Paternally Derived Aneuploidy as Detected by SNP Array?

Fertility & reproduction, 2022-09, Vol.4 (3n04), p.209-209

2022

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Preimplantation Genetic Diagnosis Update

Pathology, 2019-02, Vol.51, p.S36-S36

Hardy, Tristan

2019

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Higher Doses of FSH Used for Superovulation Do Not Adversely Affect Embryonic Ploidy: A Randomised Controlled Trial (Stimulation Resulting in Embryonic Aneuploidy Using Menopur (STREAM) Trial)

Fertility & reproduction, 2022-09, Vol.4 (3n04), p.142-142

2022

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Genetic Testing in Endocrinology

Clinical biochemist reviews, 2018-02, Vol.39 (1), p.17-28

2018

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Higher Doses of FSH Used for Superovulation Do Not Adversely Affect Embryonic Ploidy: A Randomized Controlled Trial (STimulation Resulting in Embryonic Aneuploidy using Menopur (STREAM) Trial)

Fertility & reproduction, 2021-09, Vol.3 (3), p.108-114

2021

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Placental, maternal, fetal, and technical origins of false-positive cell-free DNA screening results

American journal of obstetrics and gynecology, 2024-04, Vol.230 (4), p.381-389

2024

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A rare diagnosis of autosomal recessive recurrent biparental complete hydatidiform mole: the importance of clinical history and genetic testing

Pathology, 2024-02, Vol.56, p.S41

2024

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Impact of male age on paternal aneuploidy: single-nucleotide polymorphism microarray outcomes following blastocyst biopsy

Reproductive biomedicine online, 2023-10, Vol.47 (4), p.103245-103245, Article 103245

2023

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Recurrent pneumothorax in a case of tenascin‐X deficient Ehlers–Danlos syndrome: Broadening the phenotypic spectrum

American journal of medical genetics. Part A, 2022-05, Vol.188 (5), p.1583-1588

2022

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Recurrent pneumothorax in a case of t enascin‐X deficient Ehlers–Danlos syndrome: Broadening the phenotypic spectrum

American journal of medical genetics. Part A, 2022-05, Vol.188 (5), p.1583-1588

2022

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A Reappraisal of Circulating Fetal Cell Noninvasive Prenatal Testing

Trends in biotechnology (Regular ed.), 2019-06, Vol.37 (6), p.632-644

2019

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DCTA triplets: a fascinating trip

Pathology, 2024-02, Vol.56, p.S17-S18

2024

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Gene selection for the Australian Reproductive Genetic Carrier Screening Project ("Mackenzie's Mission")

European journal of human genetics : EJHG, 2021-01, Vol.29 (1), p.79-87

2021

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Clefting and cancer: A complex CDH1 case

Pathology, 2022-03, Vol.54, p.S14-S14

2022

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Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome

Debate 5: All Women with Recurrent Implantation Failure Should Be Offered PGT-A: Motion For – Author: Tristan Hardy; Motion Against – Author: Richard Legro

Diagnosis of adolescent polycystic ovary syndrome

Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal services

The role of prenatal diagnosis following preimplantation genetic testing for single‐gene conditions: A historical overview of evolving technologies and clinical practice

Reproductive carrier screening

Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas

Variation in the Incidence and Type of Full versus Mosaic Segmental Aneuploidies Identified in Blastocysts Undergoing PGT-A

Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes

Illuminating the Artefacts of NGS Seen in PGT-A & PGT-SR

Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium

Does Advanced Paternal Age Increase the Rate of Paternally Derived Aneuploidy as Detected by SNP Array?

Preimplantation Genetic Diagnosis Update

Higher Doses of FSH Used for Superovulation Do Not Adversely Affect Embryonic Ploidy: A Randomised Controlled Trial (Stimulation Resulting in Embryonic Aneuploidy Using Menopur (STREAM) Trial)

Genetic Testing in Endocrinology

Higher Doses of FSH Used for Superovulation Do Not Adversely Affect Embryonic Ploidy: A Randomized Controlled Trial (STimulation Resulting in Embryonic Aneuploidy using Menopur (STREAM) Trial)

Placental, maternal, fetal, and technical origins of false-positive cell-free DNA screening results

A rare diagnosis of autosomal recessive recurrent biparental complete hydatidiform mole: the importance of clinical history and genetic testing

Impact of male age on paternal aneuploidy: single-nucleotide polymorphism microarray outcomes following blastocyst biopsy

Recurrent pneumothorax in a case of tenascin‐X deficient Ehlers–Danlos syndrome: Broadening the phenotypic spectrum

Recurrent pneumothorax in a case of t enascin‐X deficient Ehlers–Danlos syndrome: Broadening the phenotypic spectrum

A Reappraisal of Circulating Fetal Cell Noninvasive Prenatal Testing

DCTA triplets: a fascinating trip

Gene selection for the Australian Reproductive Genetic Carrier Screening Project ("Mackenzie's Mission")

Clefting and cancer: A complex CDH1 case

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