H. Daum

发表

Ultrasound findings provide clues to investigate founder mutations expressed as runs of homozygosity in chromosomal microarray studies

H. Daum, I. Lerer, A. Frumkin, 2018, Prenatal diagnosis.

Is it time for prenatal chromosomal-microarray analysis to all women? A review of the diagnostic yield in structurally normal fetuses

H. Daum, S. Stern, S. Shkedi-Rafid, 2021, Current opinion in obstetrics & gynecology.

Information Women Choose to Receive About Prenatal Chromosomal Microarray Analysis.

H. Daum, A. Frumkin, S. Shkedi-Rafid, 2019, Obstetrics and gynecology.

Third‐ or Fourth‐Degree Intrapartum Anal Sphincter Tears Are Associated With Levator Ani Avulsion in Primiparas

D. Valsky, H. Daum, S. Yagel, 2016, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Failure to Thrive in the Context of Carney Complex

C. Stratakis, H. Daum, M. Lodish, 2017, Hormone Research in Paediatrics.

Detailed Transabdominal Fetal Anatomic Scanning in the Late First Trimester Versus the Early Second Trimester of Pregnancy

D. Valsky, H. Daum, S. Porat, 2015, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Single‐nucleotide polymorphism‐based chromosomal microarray analysis provides clues and insights into disease mechanisms

H. Daum, A. Frumkin, S. Yagel, 2019, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Chromosomal microarray should be performed for cases of fetal short long bones detected prenatally

H. Daum, S. Ben-Shachar, M. Khayat, 2020, Archives of Gynecology and Obstetrics.

Autosomal dominant gain of function STAT1 mutation and severe bronchiectasis.

H. Daum, E. Kerem, K. Warnatz, 2017, Respiratory medicine.

Role of late amniocentesis in the era of modern genomic technologies

H. Daum, A. Frumkin, N. Yanai, 2019, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Group A streptococcus: is there a genital carrier state in women following infection?

H. Daum, D. Stroumsa, D. Hochner-Celnikier, 2016, European Journal of Clinical Microbiology & Infectious Diseases.

The many etiologies of nonimmune hydrops fetalis diagnosed by exome sequencing

H. Daum, N. Yanai, S. Porat, 2021, Prenatal diagnosis.

Fetal exome sequencing: yield and limitations in a tertiary referral center

D. Lev, T. Harel, H. Daum, 2019, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Reversal of mirror syndrome after prenatal treatment of Diamond‐Blackfan anemia

D. Valsky, H. Daum, S. Yagel, 2007, Prenatal diagnosis.

Sonographic finding of postpartum levator ani muscle injury correlates with pelvic floor clinical examination

D. Valsky, S. Cohen, H. Daum, 2014, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Rectus Sheath Hematoma as a Rare Complication of Genetic Amniocentesis

D. Valsky, H. Daum, S. Yagel, 2007, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

BRCA mutations and reproduction.

H. Daum, T. Peretz, N. Laufer, 2018, Fertility and sterility.

Universal chromosomal microarray analysis reveals high proportion of copy‐number variants in low‐risk pregnancies

D. Valsky, H. Daum, A. Frumkin, 2020, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

An Ashkenazi founder mutation in the PKHD1 gene.

S. Carmi, H. Daum, I. Lerer, 2016, European journal of medical genetics.

Smith–Lemli–Opitz syndrome: what is the actual risk for couples carriers of the DHCR7:c.964-1G>C variant?

H. Daum, V. Meiner, J. Zlotogora, 2020, European Journal of Human Genetics.

Prevalence and Characteristics of Postpartum Vulvovaginal Atrophy and Lack of Association With Postpartum Dyspareunia

H. Daum, H. Amsalem, A. Lev-Sagie, 2020, Journal of lower genital tract disease.

Exome sequencing for structurally normal fetuses—yields and ethical issues

D. Valsky, T. Harel, H. Daum, 2022, European Journal of Human Genetics.

Third- or Fourth-Degree Intrapartum Anal Sphincter Tears Are Associated With Levator Ani Avulsion in Primiparas.

D. Valsky, H. Daum, S. Yagel, 2016, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Bi‐allelic PAGR1 variants are associated with microcephaly and a severe neurodevelopmental disorder: Genetic evidence from two families

W. Chung, H. Daum, S. Yagel, 2021, American journal of medical genetics. Part A.

GNE variants causing autosomal recessive macrothrombocytopenia without associated muscle wasting.

Sri V. V. Deevi, W. Ouwehand, K. Downes, 2018, Blood.

Congenital myopathy due to myosin heavy chain 2 mutation presenting as chronic aspiration pneumonia in infancy

H. Daum, E. Kerem, Y. Fellig, 2017, Neuromuscular Disorders.

Grandparental genotyping enhances exome variant interpretation

T. Harel, H. Daum, V. Meiner, 2020, American journal of medical genetics. Part A.

Fanconi Anemia Gene Variants in Patients with Gonadal Dysfunction

H. Daum, J. Zlotogora, 2021, Reproductive Sciences.

Detection of copy number variants associated with late-onset conditions in ~16 200 pregnancies: parameters for disclosure and pregnancy outcome

H. Daum, A. Frumkin, V. Meiner, 2022, Journal of Medical Genetics.

Monozygotic multiple gestation after intracytoplasmic sperm injection and preimplantation genetic diagnosis.

H. Daum, S. Yagel, E. Aizenman, 2009, Fertility and sterility.

Tumor STAT3 tyrosine phosphorylation status, as a predictor of benefit from adjuvant chemotherapy for breast cancer

E. Galun, L. Kadouri, H. Daum, 2013, Breast Cancer Research and Treatment.

Tissue microarray-based study of patients with lymph node-positive breast cancer shows tyrosine phosphorylation of signal transducer and activator of transcription 3 (tyrosine705-STAT3) is a marker of good prognosis

E. Galun, H. Daum, T. Peretz, 2012, Clinical and Translational Oncology.

Autosomal dominant inheritance with sex‐limited infertility

H. Daum, J. Zlotogora, 2023, American journal of medical genetics. Part A.

Persistence of levator ani sonographic defect detected by three‐dimensional transperineal sonography in primiparous women

D. Valsky, H. Daum, S. Yagel, 2015, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The Yield of Chromosomal Microarray in Pregnancies Complicated with Fetal Growth Restriction Can Be Predicted According to Clinical Parameters

H. Daum, S. Ben-Shachar, L. Sagi‐Dain, 2020, Fetal Diagnosis and Therapy.

Prenatal diagnosis of lanosterol synthase deficiency: Fetal ultrasound findings as a window on family genetics.

H. Daum, S. Porat, A. Shaag, 2023, European journal of medical genetics.