Publications by authors named "Robert D Oates"

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Genetic characterization of a missense mutation in the X-linked TAF7L gene identified in an oligozoospermic man†.
Li Ling, Fangfang Li, Pinglan Yang, Robert D Oates, Sherman Silber

Biol Reprod· July 2022

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Correction to: A contiguous microdeletion syndrome at Xp22.13 with non-obstructive azoospermia and congenital cataracts.
Aubrey Milunsky, Jeff M Milunsky, Weilai Dong, Hayk Hovhannisyan, Robert D Oates

J Assist Reprod Genet· September 2021

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Commentary on: A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens.
Robert D Oates

J Assist Reprod Genet· June 2020

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Fertility Considerations in Adolescent Klinefelter Syndrome: Current Practice Patterns.
Shalender Bhasin, Robert D Oates

J Clin Endocrinol Metab· April 2020

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A contiguous microdeletion syndrome at Xp23.13 with non-obstructive azoospermia and congenital cataracts.
Aubrey Milunsky, Jeff M Milunsky, Weilai Dong, Hayk Hovhannisyan, Robert D Oates

J Assist Reprod Genet· February 2020

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Detection of Anal Cancer at the Time of Neovaginoplasty: Is There a Role for Anal Cancer Screening Before Gender-Affirming Genital Surgery in High-Risk Patients?
James T Rague, Robert D Oates, Jaromir Slama, Carl Streed

LGBT Health· January 2020

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Forty years of IVF.
Craig Niederberger, Antonio Pellicer, Jacques Cohen, David K Gardner, Gianpiero D Palermo, Robert D Oates

Fertil Steril· July 2018

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The diagnosis of male infertility: an analysis of the evidence to support the development of global WHO guidance-challenges and future research opportunities.
Christopher L R Barratt, Lars Björndahl, Christopher J De Jonge, Dolores J Lamb, Francisco Osorio Martini, Robert D Oates

Hum Reprod Update· November 2017

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Concepts in diagnosis and therapy for male reproductive impairment.
Herman Tournaye, Csilla Krausz, Robert D Oates

Lancet Diabetes Endocrinol· July 2017

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Novel concepts in the aetiology of male reproductive impairment.
Herman Tournaye, Csilla Krausz, Robert D Oates

Lancet Diabetes Endocrinol· July 2017

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Common urologic diseases in older men and their treatment: how they impact fertility.
Gabriella Avellino, Didi Theva, Robert D Oates

Fertil Steril· February 2017

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TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.
Fang Yang, Sherman Silber, N Adrian Leu, Robert D Oates, Janet D Marszalek

EMBO Mol Med· September 2015

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Ejaculatory dysfunction.
Elizabeth Phillips, Christina Carpenter, Robert D Oates

Urol Clin North Am· February 2014

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Sperm retrieval in adolescents with Klinefelter syndrome.
Robert D Oates

Fertil Steril· October 2013

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AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.
Steven G Rozen, Janet D Marszalek, Kathryn Irenze, Helen Skaletsky, Laura G Brown, Robert D Oates

Am J Hum Genet· November 2012

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The natural history of endocrine function and spermatogenesis in Klinefelter syndrome: what the data show.
Robert D Oates

Fertil Steril· August 2012

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Clinical evaluation of the infertile male with respect to genetic etiologies.
Robert D Oates

Syst Biol Reprod Med· February 2011

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Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes.
Julian Lange, Helen Skaletsky, Saskia K M van Daalen, Stephanie L Embry, Cindy M Korver, Robert D Oates

Cell· September 2009

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The Y chromosome and male infertility.
Hossein Sadeghi-Nejad, Robert D Oates

Curr Opin Urol· November 2008

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The genetic basis of male reproductive failure.
Robert D Oates

Urol Clin North Am· May 2008

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A multi-institutional randomized controlled trial of adjuvant Web-based teaching to medical students.
B Price Kerfoot, Harley Baker, Thomas L Jackson, William C Hulbert, Daniel D Federman, Robert D Oates

Acad Med· March 2006

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Are sequence family variants useful for identifying deletions in the human Y chromosome?
Sjoerd Repping, Cindy M Korver, Robert D Oates, Sherman Silber, Fulco van der Veen

Am J Hum Genet· September 2004

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A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region.
Sjoerd Repping, Saskia K M van Daalen, Cindy M Korver, Laura G Brown, Janet D Marszalek, Robert D Oates

Genomics· June 2004

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Clinical and diagnostic features of patients with suspected Klinefelter syndrome.
Robert D Oates

J Androl· November 2003

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Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection.
Sjoerd Repping, Helen Skaletsky, Laura Brown, Saskia K M van Daalen, Cindy M Korver, Robert D Oates

Nat Genet· November 2003

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