Concepedia

Author

Dimitris Avramopoulos

Institute of Child Health

Also Known As

Avramopoulos, Dimitros, D Avramopoulos, D. Avramopoulos, Dimitris Avramopoulos

17

Publications

1.1K

Citations

13

H-Index

22

Concepts

All Affiliations

Institute of Child HealthKennedy CenterEginition HospitalJohns Hopkins UniversityJohns Hopkins Medicine
DA

About

Dimitris Avramopoulos is an author at Institute of Child Health specializing in genetics, medicine, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

5

5

654

2

Molecular Genetics

3

3

552

3

Biology

1

1

401

4

Obstetrics

1

1

35

5

Alzheimer's Disease

1

1

35

Dimitris Avramopoulos

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12

Publications

1.1K

Citations

12

H-Index

YearCitations

Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II

Neil E. Lamb, Sallie B. Freeman, Amanda Savage-Austin,

Nature Genetics

1996

401

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism

Georgia Karadima, Merete Bugge, Peter Nicolaidis,

European Journal of Human Genetics

1998

131

Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

Stylianos E. Antonarakis, J L Blouin, Jacqueline Y. Maher,

PubMed

1993

105

Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis

Constantinos Pángalos, Dimitris Avramopoulos, Jean‐Louis Blouin,

PubMed

1994

84

Apolipoprotein E allele distribution in parents of Down's syndrome children

Dimitris Avramopoulos, Maria Grigoriadou, Michael B. Petersen

The Lancet

1996

67

Normal phenotype with paternal uniparental isodisomy for chromosome 21.

J L Blouin, Dimitris Avramopoulos, Constantinos Pángalos,

PubMed

1993

62

Association between the dopamine D3 receptor gene locus (DRD3) and unipolar affective disorder

Dimitris Dikeos, G.N. Papadimitriou, Dimitris Avramopoulos,

Psychiatric Genetics

1999

58

Apolipoprotein E polymorphism in the Greek population

E. Sklavounou, E Economou-Petersen, Georgia Karadima,

Clinical Genetics

1997

47

Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome

Michael B. Petersen, Georgia Karadima, Maria Samaritaki,

American Journal of Medical Genetics

2000

35

Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype

Gotthold Barbi, Ingo Kennerknecht, Gudrun W�hr,

American Journal of Medical Genetics

2000

25

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