Huda B Al-Kouatly (H B Al-Kouatly)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 29

Top Topics

Systematic Review

Respiratory Tract

Top Venues

Prenatal diagnosis

American journal of medical genetics. Part A

Molecular genetics & genomic medicine

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

This page only lists publications with an associated author ORCID identifier.

Publications

M M Thorsen, K Khanuja, R C Mahoney, Huda B Al-Kouatly, M L Russo
Knowledge gaps and confidence in counseling about aneuploidy screening and testing: A survey of prenatal care clinicians. Prenatal diagnosis 44 (3) (2024)
Kavisha Khanuja, Jenani Jayakumaran, Huda B Al-Kouatly, Rodney A McLaren
Antenatal steroids and neonatal outcomes in late preterm births with pregestational diabetes. International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 166 (2) (2024)
Kavisha Khanuja, Jenani Jayakumaran, Huda B Al-Kouatly, Rodney A McLaren
Antenatal steroids and neonatal outcomes in late preterm births with pregestational diabetes. International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics (2024)
M M Thorsen, K Khanuja, R C Mahoney, Huda B Al-Kouatly, M L Russo
Knowledge gaps and confidence in counseling about aneuploidy screening and testing: A survey of prenatal care clinicians. Prenatal diagnosis 44 (3) (2024)
Neel S Iyer, Matthew H Mossayebi, Tracy J Gao, Lylach Haizler-Cohen, Daniele Di Mascio, Rodney A McLaren, Huda B Al-Kouatly
Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review. Molecular genetics & genomic medicine 12 (7) (2024)
Neel S Iyer, Matthew H Mossayebi, Tracy J Gao, Lylach Haizler-Cohen, Daniele Di Mascio, Rodney A McLaren, Huda B Al-Kouatly
Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review. Molecular genetics & genomic medicine 12 (7) (2024)
Stephanie M Rice, Dante F Varotsis, Sascha Wodoslawsky, Elizabeth Critchlow, Ruby Liu, Rodney A McLaren, Mona M Makhamreh, Brandy Firman, Seth I Berger, Huda B Al-Kouatly
Prenatal Phenotype of Alkuraya-Kučinskas Syndrome: A Novel Case and Systematic Literature Review. Prenatal diagnosis (2024)
M M Thorsen, K Khanuja, R C Mahoney, Huda B Al-Kouatly, M L Russo
Knowledge gaps and confidence in counseling about aneuploidy screening and testing: A survey of prenatal care clinicians. Prenatal diagnosis (2024)
M M Thorsen, K Khanuja, R C Mahoney, Huda B Al-Kouatly, M L Russo
Knowledge gaps and confidence in counseling about aneuploidy screening and testing: A survey of prenatal care clinicians. Prenatal diagnosis 44 (3) (2024)
Ariel T Levy, Sarah J Weingarten, Keely Robinson, Talia Suner, Rodney A McLaren, Antonio F Saad, Huda B Al-Kouatly
Recombinant erythropoietin for the treatment of iron deficiency anemia in pregnancy: A systematic review. International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics (2024)
Mona M Makhamreh, Kavya Shivashankar, Sarah Araji, Elizabeth Critchlow, Barbara M O'Brien, Sascha Wodoslawsky, Seth I Berger, Huda B Al-Kouatly
RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis. American journal of medical genetics. Part A 194 (5) (2023)
Mona M Makhamreh, Kavya Shivashankar, Sarah Araji, Elizabeth Critchlow, Barbara M O'Brien, Sascha Wodoslawsky, Seth I Berger, Huda B Al-Kouatly
RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis. American journal of medical genetics. Part A 194 (5) (2023)
Stephanie M Rice, Rodney A McLaren, Hiba J Mustafa, Lorraine Dugoff, Huda B Al-Kouatly
Connecting the Dots: Carrier Screening and the Genetic Information Nondiscrimination Act in the United States. Prenatal diagnosis (2023)
Huda B Al-Kouatly, Kavya Shivashankar, Matthew H Mossayebi, Mona M Makhamreh, Elizabeth Critchlow, Zimeng Gao, Luther-King Fasehun, Fowzan Sami Alkuraya, Erin E Ryan, Madhuri Hegde, Sascha Wodoslawsky, Joel Hughes, Seth I Berger
Diagnostic yield from prenatal exome sequencing for non-immune hydrops fetalis: A systematic review and meta-analysis. Clinical genetics (2023)
Mona M Makhamreh, Kavya Shivashankar, Sarah Araji, Elizabeth Critchlow, Barbara M O'Brien, Sascha Wodoslawsky, Seth I Berger, Huda B Al-Kouatly
RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis. American journal of medical genetics. Part A 194 (5) (2023)
Mona M Makhamreh, Kavya Shivashankar, Sarah Araji, Elizabeth Critchlow, Barbara M O'Brien, Sascha Wodoslawsky, Seth I Berger, Huda B Al-Kouatly
RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis. American journal of medical genetics. Part A 194 (5) (2023)
Mona M Makhamreh, Kavya Shivashankar, Sarah Araji, Elizabeth Critchlow, Barbara M O'Brien, Sascha Wodoslawsky, Seth I Berger, Huda B Al-Kouatly
RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis. American journal of medical genetics. Part A 194 (5) (2023)
Amelie Pham, Sonia Biswas, Ariel T Levy, Michail Spiliopoulos, Rodney McLaren, Mona M Makhamreh, Huda B Al-Kouatly
Imaging and outcomes of fetal adrenal hemorrhage: A systematic review. Prenatal diagnosis (2023)
Casey J Brewer, Mona M Makhamreh, Kavya Shivashankar, Rodney McLaren, Mariella Toro, Seth I Berger, Huda B Al-Kouatly
PIEZO1 is the most common monogenic etiology of non-immune hydrops fetalis detected by prenatal exome sequencing. Prenatal diagnosis (2023)
Mona M Makhamreh, Kavya Shivashankar, Sarah Araji, Elizabeth Critchlow, Barbara M O'Brien, Sascha Wodoslawsky, Seth I Berger, Huda B Al-Kouatly
RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis. American journal of medical genetics. Part A (2023)
Elizabeth Critchlow, Sascha Wodoslawsky, Mona M Makhamreh, Stephanie M Rice, Ozhan M Turan, Brandy Firman, Rodney A McLaren, Sarah Araji, Huda B Al-Kouatly
Maternal outcomes of a cohort of pregnancies affected by non-immune hydrops fetalis. International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics (2023)
Mona M Makhamreh, Kavya Shivashankar, Sarah Araji, Elizabeth Critchlow, Barbara M O'Brien, Sascha Wodoslawsky, Seth I Berger, Huda B Al-Kouatly
RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis. American journal of medical genetics. Part A 194 (5) (2023)
Mona M Makhamreh, Kavya Shivashankar, Sarah Araji, Elizabeth Critchlow, Barbara M O'Brien, Sascha Wodoslawsky, Seth I Berger, Huda B Al-Kouatly
RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis. American journal of medical genetics. Part A 194 (5) (2023)
Rebecca Horgan, Elizabeth Critchlow, Sascha Wodoslawsky, Stephanie M Rice, Jonathan L Hecht, Huda B Al-Kouatly
Placental phenotype in non-immune hydrops fetalis with negative standard workup. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 60 (5) (2022)
Neel S Iyer, Alexis C Gimovsky, Carlos R Ferreira, Elizabeth Critchlow, Huda B Al-Kouatly
Lysosomal storage disorders as an etiology of nonimmune hydrops fetalis: A systematic review. Clinical genetics 100 (5) (2021)
Marie Cosette Gabriel, Stephanie M Rice, Jennifer L Sloan, Matthew H Mossayebi, Charles P Venditti, Huda B Al-Kouatly
Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria. Molecular genetics & genomic medicine 9 (4) (2021)
Kate Swanson, Juliet C Bishop, Huda B Al-Kouatly, Mona Makhamreh, Thomas Felton, Neeta L Vora, Teresa N Sparks, Angie C Jelin
Prenatal phenotype of 47, XXY (Klinefelter syndrome). Prenatal diagnosis (2021)
Cheryl Godcharles, Melody Safarzadeh, Emily A Oliver, Amanda Roman, Huda B Al-Kouatly
Phrenic nerve injury secondary to extracorporeal membrane oxygenation in pregnancy: A case report. Clinical case reports 8 (10) (2020)
Julie Gomez, Stephanie M Rice, Mona M Makhamreh, Huda B Al-Kouatly
Pregnancy management in a patient with stickler syndrome. Molecular genetics & genomic medicine 8 (8) (2020)