P. Ray

发表

Five years' experience of preimplantation genetic diagnosis in the Parisian Center: outcome of the first 441 started cycles.

N. Frydman, R. Frydman, E. Feyereisen, 2007, Fertility and sterility.

CFAP61 is required for sperm flagellum formation and male fertility in human and mouse

P. Ray, Siyu Liu, Jintao Zhang, 2021, bioRxiv.

The genetic architecture of morphological abnormalities of the sperm tail

P. Ray, Zine-Eddine Kherraf, Caroline Cazin, 2020, Human Genetics.

Genetic causes of male infertility: snapshot on morphological abnormalities of the sperm flagellum

P. Ray, C. Coutton, C. Arnoult, 2019, Basic and Clinical Andrology.

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

A. Munnich, B. Gener, S. Lyonnet, 2003, Nature Genetics.

Absence of Dpy19l2, a new inner nuclear membrane protein, causes globozoospermia in mice by preventing the anchoring of the acrosome to the nucleus

P. Ray, C. Coutton, C. Arnoult, 2012, Development.

Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome and recurrent intrauterine fetal death

R. Bouvier, P. Ray, A. Vasiljevic, 2015, The Lancet.

Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility

Klaus Dieterich, Pierre-Simon Jouk, Sophie Rousseaux, 2007, Nature Genetics.

Deciphering the genetics of male infertility: progress and challenges.

P. Ray, 2011, The Journal of urology.

A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis.

P. Ray, J. Lunardi, R. Zouari, 2011, Molecular human reproduction.

Identification of a new recurrent aurora kinase C mutation in both European and African men with macrozoospermia.

M. Blum, P. Jouk, S. Viville, 2012, Human Reproduction.

Quantitative measurement of transcript levels throughout human preimplantation development: analysis of hypoxanthine phosphoribosyl transferase.

P. Ray, A. Ao, A. Handyside, 2001, Molecular human reproduction.

Genetics of teratozoospermia: Back to the head.

P. Ray, Zine-Eddine Kherraf, Caroline Cazin, 2020, Best practice & research. Clinical endocrinology & metabolism.

AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice

A. Monaco, Z. Molnár, P. Ray, 2018, Scientific Reports.

Genetic abnormalities leading to qualitative defects of sperm morphology or function

M. Mitchell, P. Ray, C. Metzler-Guillemain, 2017, Clinical genetics.

MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia.

P. Jouk, F. Abada, P. Ray, 2012, Human reproduction.

Preimplantation genetic diagnosis (PGD), a collaborative activity of clinical genetic departments and IVF centres

L. Gianaroli, E. Kanavakis, S. Viville, 2001, Prenatal diagnosis.

Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.

P. Tufféry, P. Ray, T. Dirami, 2013, American journal of human genetics.

Denaturing high‐performance liquid chromatography (DHPLC)‐based prenatal diagnosis for tuberous sclerosis

P. Bénit, A. Munnich, P. Ray, 2001, Prenatal diagnosis.

Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.

N. Thierry-Mieg, S. Brouillet, P. Ray, 2018, American journal of human genetics.

Paternal epigenetics: Mammalian sperm provide much more than DNA at fertilization

P. Ray, C. Arnoult, Emilie Le Blévec, 2020, Molecular and Cellular Endocrinology.

Oligogenic heterozygous inheritance of sperm abnormalities in mouse

P. Ray, S. Nef, Zine-Eddine Kherraf, 2022, eLife.

Creation of knock out and knock in mice by CRISPR/Cas9 to validate candidate genes for human male infertility, interest, difficulties and feasibility

B. Conne, P. Ray, S. Nef, 2018, Molecular and Cellular Endocrinology.

Snake venoms as a source of compounds modulating sperm physiology: Secreted phospholipases A2 from Oxyuranus scutellatus scutellatus impact sperm motility, acrosome reaction and in vitro fertilization in mice.

G. Lambeau, P. Ray, M. De Waard, 2010, Biochimie.

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

N. Thierry-Mieg, B. Conne, P. Jouk, 2018, Nature Communications.

Pantoprazole, a proton‐pump inhibitor, impairs human sperm motility and capacitation in vitro

P. Ray, S. Nef, C. Arnoult, 2020, Andrology.

Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis

A. Munnich, N. Frydman, R. Fanchin, 2005, Journal of Medical Genetics.

A new mutation identified in SPATA16 in two globozoospermic patients

S. Viville, P. Ray, A. Saâd, 2016, Journal of Assisted Reproduction and Genetics.

Subcellular localization of phospholipase Cζ in human sperm and its absence in DPY19L2-deficient sperm are consistent with its role in oocyte activation.

P. Ray, C. Metzler-Guillemain, C. Coutton, 2015, Molecular human reproduction.

ESHRE preimplantation genetic diagnosis consortium: Data collection III (May 2001)

S. Viville, K. Sermon, C. Staessen, 2002 .

Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction

P. Jouk, H. Sartelet, P. Ray, 2018, Clinical genetics.

Treatment of Mouse Sperm with a Non-Catalytic Mutant of PLA2G10 Reveals That PLA2G10 Improves In Vitro Fertilization through Both Its Enzymatic Activity and as Ligand of PLA2R1

G. Lambeau, P. Ray, C. Arnoult, 2022, International journal of molecular sciences.

The effect of group X secreted phospholipase A2 on fertilization outcome is specific and not mimicked by other secreted phospholipases A2 or progesterone.

G. Lambeau, P. Ray, C. Arnoult, 2014, Biochimie.

Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome

P. Jouk, P. Ray, J. Lunardi, 2010, Prenatal diagnosis.

Clinical applications of fetal sex determination in maternal blood in a preimplantation genetic diagnosis centre.

N. Frydman, R. Frydman, P. Ray, 2002, Human reproduction.

The essential role of intraflagellar transport protein IFT81 in male mice spermiogenesis and fertility.

Qi Zhou, C. Quan, P. Ray, 2020, American journal of physiology. Cell physiology.

Increased number of cells and metabolic activity in male human preimplantation embryos following in vitro fertilization.

P. Ray, A. Handyside, J. Conaghan, 1995, Journal of reproduction and fertility.

A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females

N. Thierry-Mieg, P. Ray, Zine-Eddine Kherraf, 2022, Clinical genetics.

Single cell multiplex PCR amplification of five dystrophin gene exons combined with gender determination.

A. Munnich, P. Ray, M. Vekemans, 2001, Molecular human reproduction.

Increasing the denaturation temperature during the first cycles of amplification reduces allele dropout from single cells for preimplantation genetic diagnosis.

P. Ray, A. Handyside, A. Handyside, 1996, Molecular human reproduction.

Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28

A. Munnich, N. Frydman, R. Frydman, 2004, Human Genetics.

Progesterone-induced Acrosome Exocytosis Requires Sequential Involvement of Calcium-independent Phospholipase A2β (iPLA2β) and Group X Secreted Phospholipase A2 (sPLA2)*

G. Lambeau, J. Turk, P. Ray, 2015, The Journal of Biological Chemistry.

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.

M. Ikawa, P. Ray, L. Jin, 2020, American journal of human genetics.

Improved single-cell protocol for preimplantation genetic diagnosis of spinal muscular atrophy.

A. Munnich, N. Frydman, R. Frydman, 2005, Fertility and sterility.

Reduced allele dropout in single-cell analysis for preimplantation genetic diagnosis of cystic fibrosis

P. Ray, A. Handyside, R. Winston, 1996, Journal of Assisted Reproduction and Genetics.

Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice.

Shimin Zhao, P. Ray, L. Jin, 2019, American journal of human genetics.

Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice

P. Ray, L. Jin, Yunxia Cao, 2019, Journal of Medical Genetics.

The sperm associated antigen 6 interactome and its role in spermatogenesis.

U. Knippschild, C. Cho, P. Ray, 2019, Reproduction.

Enzymatic activity of mouse group X-sPLA2 improves in vitro production of preimplantation bovine embryos.

P. Mermillod, G. Lambeau, P. Ray, 2019, Theriogenology.

DPY19L2 deletion as a major cause of globozoospermia.

C. Redin, S. Viville, P. Ray, 2011, American journal of human genetics.

The genetic architecture of morphological abnormalities of the sperm tail

P. Ray, Zine-Eddine Kherraf, Caroline Cazin, 2020, Human Genetics.

Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations

N. Thierry-Mieg, P. Ray, H. Gourabi, 2019, Clinical genetics.

Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH 2 mutations

N. Thierry-Mieg, P. Ray, H. Gourabi, 2019 .

Patients with multiple morphological abnormalities of the sperm flagella due to DNAH1 mutations have a good prognosis following intracytoplasmic sperm injection.

S. Brouillet, P. Ray, C. Coutton, 2016, Human reproduction.

Single gene defects leading to sperm quantitative anomalies

M. Mitchell, P. Ray, C. Metzler-Guillemain, 2017, Clinical genetics.

Paternal transcripts for glucose‐6‐phosphate dehydrogenase and adenosine deaminase are first detectable in the human preimplantation embryo at the Three‐ to Four‐Cell stage

P. Ray, A. Ao, A. Handyside, 1997, Molecular reproduction and development.

Spermaurin, an La1-like peptide from the venom of the scorpion Scorpio maurus palmatus, improves sperm motility and fertilization in different mammalian species

P. Ray, P. Bulet, E. Schmitt, 2016, Molecular human reproduction.

Oligogenic heterozygous inheritance of sperm abnormalities in mouse

P. Ray, S. Nef, Zine-Eddine Kherraf, 2021, bioRxiv.

Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia.

N. Thierry-Mieg, P. Ray, L. Raymond, 2022, American journal of human genetics.

SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes

Thomas Karaouzene, Nicolas Thierry-Mieg, Serge Nef, 2017, EMBO molecular medicine.

Teratozoospermia: spotlight on the main genetic actors in the human.

P. Ray, C. Coutton, C. Arnoult, 2015, Human reproduction update.

Mutations of the aurora kinase C gene causing macrozoospermia are the most frequent genetic cause of male infertility in Algerian men

P. Ray, J. Fauré, C. Coutton, 2014, Asian journal of andrology.

Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice.

N. Thierry-Mieg, B. Conne, P. Ray, 2019, American journal of human genetics.

A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.

P. Jouk, S. Viville, F. Abada, 2011, American journal of human genetics.

Group X secreted phospholipase A2 specifically decreases sperm motility in mice

G. Lambeau, P. Ray, M. De Waard, 2011, Journal of cellular physiology.

Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.

P. Ray, S. Savinov, F. Guillonneau, 2019, American journal of human genetics.

Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia

S. Amselem, P. Ray, S. Savinov, 2018, Human molecular genetics.

Allelic drop-out and preferential amplification in single cells and human blastomeres: implications for preimplantation diagnosis of sex and cystic fibrosis.

P. Quirke, R. Lilford, P. Ray, 1995, Human reproduction.

Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility.

J. Veltman, M. O’Bryan, P. Ray, 2021, American journal of human genetics.

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.

Y. Li, Yong-Gang Yao, Zhixi Su, 2023, American journal of human genetics.

Rapid Proteomic Profiling by MALDI‐TOF Mass Spectrometry for Better Brain Tumor Classification

J. Rendu, P. Ray, C. Coutton, 2020, Proteomics. Clinical applications.

XIST expression from the maternal X chromosome in human male preimplantation embryos at the blastocyst stage.

P. Ray, A. Handyside, R. Winston, 1997, Human molecular genetics.

Diversity of RNA-Binding Proteins Modulating Post-Transcriptional Regulation of Protein Expression in the Maturing Mammalian Oocyte

P. Ray, C. Arnoult, E. Lambert, 2020, Cells.

Preimplantation genetic diagnosis of β-thalassaemia major

P. Ray, A. Handyside, I. Roberts, 1996, The Lancet.

PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice

N. Thierry-Mieg, B. Conne, P. Ray, 2018, EMBO Molecular Medicine.

Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa

N. Thierry-Mieg, P. Ray, Zine-Eddine Kherraf, 2021, International journal of molecular sciences.

A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility.

M. Blum, N. Thierry-Mieg, P. Ray, 2018, American journal of human genetics.

KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole.

P. Ray, M. Totonchi, Navid Almadani, 2021, European journal of obstetrics, gynecology, and reproductive biology.

CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report.

N. Thierry-Mieg, S. Brouillet, P. Ray, 2019, Human reproduction.

Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.

N. Thierry-Mieg, D. Grunwald, P. Jouk, 2014, American journal of human genetics.

Dpy19l2-deficient globozoospermic sperm display altered genome packaging and DNA damage that compromises the initiation of embryo development.

J. Ravanat, P. Ray, C. Metzler-Guillemain, 2015, Molecular human reproduction.

Current status of preimplantation diagnosis

C. Strom, K. Sermon, A. Kuliev, 1997, Journal of Assisted Reproduction and Genetics.

Microduplication of the ARID1A gene causes intellectual disability with recognizable syndromic features

J. Clayton-Smith, P. Jouk, J. Thevenon, 2016, Genetics in Medicine.

Fine Characterisation of a Recombination Hotspot at the DPY19L2 Locus and Resolution of the Paradoxical Excess of Duplications over Deletions in the General Population

N. Thierry-Mieg, P. Jouk, F. Abada, 2013, PLoS genetics.

PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans

F. Béna, R. Christensen, P. Jouk, 2017, Journal of Medical Genetics.

Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player

N. Thierry-Mieg, L. Pasquier, Flore Mietton, 2020, Human Genetics.

Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player

N. Thierry-Mieg, L. Pasquier, Flore Mietton, 2020, Human genetics.

Reproductive genetics MLPA and sequence analysis of DPY 19 L 2 reveals point mutations causing globozoospermia

P. Jouk, F. Abada, P. Ray, 2012 .

The involvement of the nuclear lamina in human and rodent spermiogenesis: a systematic review

M. Mitchell, N. Lévy, P. Ray, 2018, Basic and Clinical Andrology.

First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiency

A. Munnich, N. Frydman, R. Frydman, 2000, Prenatal diagnosis.

AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice

A. Monaco, Z. Molnár, P. Ray, 2018, Scientific Reports.

Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.

M. Sabbaghian, P. Ray, M. Sanati, 2016, Human reproduction.

Birth of healthy female twins after preimplantation genetic diagnosis of cystic fibrosis combined with gender determination.

A. Munnich, N. Frydman, R. Frydman, 2002, Molecular human reproduction.

CLINICAL EXPERIENCE WITH PREIMPLANTATION GENETIC DIAGNOSIS OF CYSTIC FIBROSIS (ΔF508)

J. Harper, P. Ray, A. Ao, 1996 .

Clinical experience with preimplantation genetic diagnosis of cystic fibrosis (delta F508).

J. Harper, P. Ray, A. Ao, 1996, Prenatal Diagnosis.

Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella

N. Thierry-Mieg, P. Ray, Zine-Eddine Kherraf, 2018, Human reproduction.

Assessment of the reliability of single blastomere analysis for preimplantation diagnosis of the ΔF508 deletion causing cystic fibrosis in clinical practice

P. Ray, A. Ao, A. Handyside, 1998, Prenatal diagnosis.

The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility

N. Thierry-Mieg, P. Santulli, P. Ray, 2021, Clinical genetics.

Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility

N. Thierry-Mieg, P. Ray, Y. Fichou, 2020, Journal of Medical Genetics.

Novel axonemal protein ZMYND12 is required for flagellum function and male fertility

N. Thierry-Mieg, P. Ray, J. Dupuy, 2023 .

Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human

A. Leenhardt, V. Probst, P. Ray, 2012, Human molecular genetics.

Lack of CCDC 146 , a ubiquitous centriole and microtubule-associated protein , 2 leads to non-syndromic male infertility in human and mouse 3 4 5

N. Thierry-Mieg, S. Geimer, P. Ray, 2023 .

Defect in the nuclear pore membrane glycoprotein 210-like gene is associated with extreme uncondensed sperm nuclear chromatin and male infertility: a case report.

N. Thierry-Mieg, P. Ray, A. Loundou, 2020, Human reproduction.

CFAP61 is required for sperm flagellum formation and male fertility in human and mouse.

P. Ray, Siyu Liu, Jintao Zhang, 2021, Development.

New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella

N. Thierry-Mieg, P. Ray, Zine-Eddine Kherraf, 2023, International journal of molecular sciences.

Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes C1orf185 and CCT6B

N. Thierry-Mieg, P. Ray, S. Nef, 2021, Cells.

A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome

N. Thierry-Mieg, P. Ray, Zine-Eddine Kherraf, 2021, Human Genetics.

[Contribution of genotyping for fetal sex determination in maternal serum for preimplantation genetic diagnosis of X-linked diseases].

N. Frydman, R. Frydman, P. Ray, 2003, Gynecologie, obstetrique & fertilite.

PCR from single cells for preimplantation diagnosis.

P. Ray, A. Handyside, 1996, Methods in molecular medicine.

The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population.

P. Jouk, S. Viville, P. Ray, 2009, Human molecular genetics.

[Function of aurora kinase C (AURKC) in human reproduction].

P. Ray, J. Lunardi, R. Zouari, 2009, Gynécologie Obstétrique & Fertilité.

Can intracytoplasmic morphologically selected sperm injection be used to select normal-sized sperm heads in infertile patients with macrocephalic sperm head syndrome?

P. Ray, F. Vialard, M. Chelli, 2010, Fertility and sterility.

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

N. Thierry-Mieg, B. Conne, P. Jouk, 2018, Nature Communications.

Understanding the genetics of human infertility

P. Ray, Qing Sang, Lei Wang, 2023, Science.

[Genetics of male infertility: the new players].

P. Ray, C. Coutton, C. Arnoult, 2012, Medecine sciences : M/S.

Inverse correlation between chromatin condensation and sperm head size in a case of enlarged sperm heads.

P. Ray, F. Vialard, J. Selva, 2011, Reproductive biomedicine online.

Corrigendum: Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia.

S. Amselem, P. Ray, S. Savinov, 2018, Human molecular genetics.

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

N. Thierry-Mieg, B. Conne, P. Jouk, 2018, Nature Communications.

Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP.

N. Thierry-Mieg, P. Ray, S. Savinov, 2016, Human molecular genetics.

[First birth after preimplantation genetic diagnosis performed on thawed embryos].

N. Frydman, R. Fanchin, R. Frydman, 2003, Journal de gynecologie, obstetrique et biologie de la reproduction.

[Preimplantation genetic diagnosis experience in Paris: evaluation of first births].

A. Munnich, R. Frydman, S. Romana, 2002, Journal de gynecologie, obstetrique et biologie de la reproduction.

Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCR.

A. Munnich, N. Frydman, R. Frydman, 2005, Molecular genetics and metabolism.

The place of 'social sexing' in medicine and science.

A. Munnich, R. Frydman, S. Viville, 2002, Human reproduction.

Evolution of preimplantation genetic diagnosis in France.

P. Ray, 2001, Reproductive biomedicine online.

Successful preimplantation genetic diagnosis for sex linked Lesch–Nyhan syndrome using specific diagnosis

J. Harper, P. Ray, A. Ao, 1999, Prenatal diagnosis.

Correction: Dynamics of Sun5 Localization during Spermatogenesis in Wild Type and Dpy19l2 Knock-Out Mice Indicates That Sun5 Is Not Involved in Acrosome Attachment to the Nuclear Envelope

P. Ray, C. Arnoult, J. Escoffier, 2015, PloS one.

Dynamics of Sun5 Localization during Spermatogenesis in Wild Type and Dpy19l2 Knock-Out Mice Indicates That Sun5 Is Not Involved in Acrosome Attachment to the Nuclear Envelope

P. Ray, C. Arnoult, J. Escoffier, 2015, PloS one.

Sun proteins and Dpy19l2 forming LINC-like links are critical for spermiogenesis

P. Ray, C. Coutton, C. Arnoult, 2016, Biology Open.

Preimplantation diagnosis of genetic and chromosomal disorders

C. Readhead, N. Arnheim, C. Strom, 1994, Journal of Assisted Reproduction and Genetics.

Chronology of reported denaturing high performance liquid chromatography (DHPLC)‐based prenatal diagnoses

P. Bénit, A. Munnich, P. Ray, 2003, Prenatal diagnosis.

Comparative testicular transcriptome of wild type and globozoospermic Dpy19l2 knock out mice

P. Ray, C. Coutton, C. Arnoult, 2013, Basic and Clinical Andrology.

O▪26 Preimplantation diagnosis of the NARP mitochondrial DNA mutation

A. Munnich, N. Frydman, R. Frydman, 2005 .

Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function

N. Thierry-Mieg, P. Ray, J. Dupuy, 2023, bioRxiv.

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse

N. Thierry-Mieg, Kuokuo Li, F. Tao, 2021, Human Genetics.

Whole-exome sequencing identi fi es mutations in FSIP 2 as a recurrent cause of multiple morphological abnormalities of the sperm fl agella

N. Thierry-Mieg, P. Ray, C. Coutton, 2018 .

Absence of CFAP 69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse

N. Thierry-Mieg, S. Brouillet, P. Ray, 2018 .

Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans

N. Thierry-Mieg, P. Ray, Caroline Cazin, 2023, iScience.

Genetic causes of macrozoospermia and proposal for an optimized genetic diagnosis strategy based on sperm parameters.

N. Thierry-Mieg, P. Ray, E. Bieth, 2023, Journal of genetics and genomics = Yi chuan xue bao.

[AFU and SALF recommendations for the evaluation of male infertility].

P. Ray, F. Eustache, W. Akakpo, 2020, Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie.

Progesterone-induced Acrosome Exocytosis Requires Sequential Involvement of Calcium-independent Phospholipase A2β (iPLA2β) and Group X Secreted Phospholipase A2 (sPLA2)*

G. Lambeau, J. Turk, P. Ray, 2015, The Journal of Biological Chemistry.

Microduplication of the ARID1A gene causes intellectual disability with recognizable syndromic features

J. Clayton-Smith, P. Jouk, J. Thevenon, 2016, Genetics in Medicine.

A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.

P. Jouk, S. Viville, F. Abada, 2011, American journal of human genetics.

CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans.

P. Ray, Caroline Cazin, A. Touré, 2023, Clinical Genetics.

Absence of Dpy19l2, a new inner nuclear membrane protein, causes globozoospermia in mice by preventing the anchoring of the acrosome to the nucleus

P. Ray, C. Coutton, C. Arnoult, 2012, Development.

Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse

S. Geimer, P. Ray, N. Klena, 2023, bioRxiv.

Sex selection by preimplantation genetic diagnosis: should it be carried out for social purposes?Is preimplantation genetic diagnosis for ‘social sexing’ desirable in today's and tomorrow's society?

A. Munnich, R. Frydman, S. Viville, 2003 .

From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the ZMYND15 gene

P. Ray, Caroline Cazin, C. Coutton, 2022, Asian journal of andrology.