Skip to main content

Table 1 A list of projects that contributed data1

From: Enhanced genetic maps from family-based disease studies: population-specific comparisons

PI

(last name)

Number

of persons

genotyped

Number

of

pedigrees

Number

of

markers

Weber

Set

Ethnicity

PubMed ID

Bell

602

60

386

9

European (Europe)

14500288

Berrettini

689

202

386

9

European (Europe)

11799475

Berrettini

899

329

361

9

European (USA2)

11799475

Boomsma

917

219

405

10

European (Europe)

17700629, 16899170

Cantor

347

71

402

10

European (USA)

15476245

Catalona

513

232

387

9

European (USA)

11309685

Cho

701

196

387

9

European (USA)

15472510

Concannon

465

111

387

9

European (USA)

11507694

Concannon

461

110

386

9

European (USA)

11507694

DeLisi

446

114

404

10

Hispanic (Costa Rica)

12116183

Duerr

439

96

386

9

European (USA)

10747815

Duerr

605

126

386

9

European (USA)

10747815

Hunt

3322

948

391

9

African American

12068377

Jacob

1041

375

402

10

European (Europe)

11818963

Jacob

550

191

402

10

European (Europe)

11818963

Klein

542

96

404

10

European (USA)

12900797

Klein

130

22

386

9

European (USA)

12900797

Kuivaniemi

140

38

402

10

European (Europe, USA, Canada)

15096456

Leal

153

11

386

9

European (Europe)

10777717

Murray

756

173

387

9

European (Europe, USA), Chinese

12087515

Myles- Worsley

275

18

404

10

Palauan

15915326

Pirastu

877

197

403

10

European (Europe)

15478097

Vats

220

23

404

10

Unknown3

12819239

Weiss

1128

279

404

10

Chinese

11673820

Xu

745

168

388

9

Chinese

10330357

Xu

749

172

387

9

Chinese

10330357

  1. 1 Two additional PIs, A. Shuldiner and and G. Tromp, sent data for studies using Weber screening set 8 and 11. Since these were the only datasets that didn't use screening set 9 or 10 we opted to exclude them from our analyses.
  2. 2 These samples are individuals of European descent living in the United States (USA).
  3. 3 The ethnicity for the samples in this set was not available. Therefore, this set was only used for the initial CRI-MAP map which was used to determine starting points for the full-likelihood map.