A. Asamoah

发表

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.

Donna M. Martin, B. Coe, J. Rosenfeld, 2012, The New England journal of medicine.

Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes

S. Scherer, J. Rosenfeld, A. V. Vulto-van Silfhout, 2016, Molecular Psychiatry.

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.

Klaus Lehnert, Holger Lerche, Annapurna Poduri, 2018, American journal of human genetics.

Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low‐copy repeats

Stephanie E. Vallee, J. Rosenfeld, L. Shaffer, 2012, Human mutation.

Contribution of P. falciparum parasites with Pfhrp 2 gene deletions to false negative PfHRP 2 based malaria RDT results in Ghana: A nationwide study of symptomatic malaria patients

L. Amoah, A. Asamoah, B. Abuaku, 2020, PloS one.

Diarrhoea morbidity patterns in Central Region of Ghana

S. Sackey, K. Nyarko, E. Afari, 2016, The Pan African medical journal.

Impact of malaria diagnostic refresher training programme on competencies and skills in malaria diagnosis among medical laboratory professionals: evidence from Ghana 2015–2019

A. Asamoah, J. Nonvignon, K. Malm, 2021, Malaria journal.

Memory and Learning in Children with 22q11.2 Deletion Syndrome: Evidence for Ventral and Dorsal Stream Disruption?

E. Bigler, A. Asamoah, J. Titus, 2005, Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence.

A deletion in the angiotensin converting enzyme (ACE) gene is common among African Americans with essential hypertension

A. Asamoah, K. Yanamandra, T. Thurmon, 1996 .

Use of 86Rb and 22Na in assaying active and cotransport activities in human erythrocytes in a biracial population.

D. Freedman, G. Berenson, A. Asamoah, 1988, Clinica chimica acta; international journal of clinical chemistry.

Identification of ectodysplasin-A receptor gene deletion at 2q12.2 and a potential autosomal MR locus

A. Srivastava, B. Dupont, A. Asamoah, 2009, European Journal of Human Genetics.

Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay

A. Asamoah, D. V. Van Dyke, A. Wiktor, 2003, American journal of medical genetics. Part A.

Diagnosis of Classic Homocystinuria in Two Boys Presenting with Acute Cerebral Venous Thrombosis and Neurologic Dysfunction after Normal Newborn Screening

A. Asamoah, K. Jackson, J. Hersh, 2021, International journal of neonatal screening.

Gendered School Experiences: The impact on Retention and Achievement in Botswana and Ghana

M. Dunne, B. Chilisa, N. Kutor, 2005 .

Laboratory evaluation of homocysteine remethylation disorders and classic homocystinuria: long-term follow-up using a cohort of 123 patients.

T. Yuzyuk, N. Longo, A. Asamoah, 2020, Clinica chimica acta; international journal of clinical chemistry.

Spontaneous corneal rupture in Noonan syndrome. A case report.

A. Asamoah, J. Patel, Y. Au, 1997, Ophthalmic genetics.

A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay

Deborah L. Levy, Gregory M. Cooper, Brian L. Browning, 2010, Nature Genetics.

Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.

B. Pletcher, J. Knoll, J. Wagstaff, 1995, American journal of medical genetics.

Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.

William W. Cohen, L. Shaffer, E. Zackai, 2009, Human molecular genetics.

Perinatal Autopsy Findings in Three Cases of Jugular Lymphatic Obstruction Sequence and Cardiac Polyvalvular Dysplasia

A. Asamoah, R. Bendon, 2008, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2–p12.2

U. Surti, L. Shaffer, E. Zackai, 2007, Nature Genetics.

Nationwide molecular surveillance of three Plasmodium species harboured by symptomatic malaria patients living in Ghana

L. Amoah, A. Asamoah, B. Abuaku, 2022, Parasites & vectors.

Novel LMNA mutations in patients with Emery‐Dreifuss muscular dystrophy and functional characterization of four LMNA mutations

Juliet A. Ellis, J. Mendell, S. Iannaccone, 2011, Human mutation.

Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.

Matthew H. Brush, David R. Murdock, Jean M. Davidson, 2019, Biological psychiatry.

Congenital Chylothorax in Neonatal Thyrotoxicosis

A. Asamoah, A. Pramanik, Patricia Webster, 1999, Journal of Perinatology.

Molecular characterization of distal 4q duplication in two patients using oligonucleotide array‐based comparative genomic hybridization (oaCGH) analysis

A. Asamoah, G. Gowans, Kathryn Platky, 2014, American journal of medical genetics. Part A.

Unusual Metabolites in a Patient with Isovaleric Acidemia.

M. Pasquali, A. Asamoah, I. De Biase, 2019, Clinical chemistry.

Segregation and linkage analyses of dopamine-beta-hydroxylase activity in a six-generation pedigree.

R. Elston, G. Berenson, A. Asamoah, 1987, American journal of medical genetics.

Genotypic glucose-6-phosphate dehydrogenase (G6PD) deficiency protects against Plasmodium falciparum infection in individuals living in Ghana

L. Amoah, J. Abankwa, A. Asamoah, 2021, PloS one.

Assessing malaria staining practices with Giemsa for malaria microscopy; a case of selected laboratory facilities in the Ashanti region of Ghana

Michael Addai, A. Asamoah, B. A. Owusu, 2022, Scientific African.

A case of insertional translocation involving chromosomes 2 and 4

Harold Chen, A. Asamoah, L. Prouty, 1998, Clinical genetics.

The neuropsychological phenotype of velocardiofacial syndrome (VCFS): relationship to psychopathology.

R. Lajiness-O'Neill, A. Asamoah, J. Titus, 2006, Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists.

Factors Associated With Antimicrobial Self-Medication in Birim Central Municipal of Eastern Region Ghana

A. Asamoah, 2019 .

Fetal alcohol spectrum disorders: guidance for recognition, diagnosis, differential diagnosis and referral.

Y. Senturias, A. Asamoah, 2014, Current problems in pediatric and adolescent health care.

Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

A. Singleton, T. Rinne, J. Christodoulou, 2018, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Heme and sensory neuropathy: insights from novel mutations in the heme exporter feline leukemia virus subgroup C receptor 1

F. Altruda, E. Tolosano, E. Bellacchio, 2019, Pain.

Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2

B. Torchia, J. Coppinger, B. Bejjani, 2010, Clinical genetics.

17q inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type one.

B. Korf, K. North, J. Wagstaff, 1995, American journal of medical genetics.

Malaria parasitaemia and mRDT diagnostic performances among symptomatic individuals in selected health care facilities across Ghana

L. Amoah, A. Asamoah, B. Abuaku, 2021, BMC Public Health.

Therapeutic efficacy of dihydroartemisinin-piperaquine combination for the treatment of uncomplicated malaria in Ghana

A. Asamoah, K. Koram, B. Abuaku, 2023, Frontiers in Cellular and Infection Microbiology.

Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes

Matthew J. Thomas, J. Rosenfeld, B. Torchia, 2012, European Journal of Human Genetics.

Emicizumab Associated Rhabdomyolysis in Hemophilia A

A. Raj, A. Asamoah, Vivek R. Sharma, 2020, Clinical Hematology International.

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.

I. Scheffer, H. Mefford, E. Haan, 2019, American Journal of Human Genetics.

A major gene model for the familial aggregation of plasma IgA concentration

Alexander F. Wilson, R. Elston, B. Julian, 1987, American journal of medical genetics.

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.

Bradley P. Coe, Donna M. Martin, J. Rosenfeld, 2012, The New England journal of medicine.

Nationwide Surveillance of Pfhrp2 Exon 2 Diversity in Plasmodium falciparum Circulating in Symptomatic Malaria Patients Living in Ghana.

Colby T. Ford, L. Amoah, A. Asamoah, 2022, The American journal of tropical medicine and hygiene.